, rnulti-qua ntum-we ll lasers." Truu.:
IEeE
S.
3d ed.. \\/lIc:y New York. 1900.
}/)/I. £63, 102-LO~ ( 1%5).
47~
SEfvlICONDUCTOR LASERS
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»:
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T. Tsang, M. C. WlI, T. Tanbun-Ek, R . A. Logan, S. N. G. Chu, and A. M. Sergent, "Low-threshold and high-power output J .5-,um InGaAsj InGnAsP separate confinement multiple quantum well laser grown by chemical beam epitaxy." Appl. Phys. Lett. 57,..-2065-2067 (990).
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.............. ,...
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..., ....
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... ... '
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I);' :Halheni(ltico! Functions,
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4R2
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Pj\RT IV Modulation of Light
•
11 Direct Modulation of Semiconductor Lasers For a sem icond uctor laser, the output power of light intensity P increases linearly with the injection current above threshold, as discussed in Section 10.1, Eq . (10.1.31): h co
P
=
qTfi
In(l/R) cr.L + In l/R (1 - 1tlt )
Therefore, for an injection current with a dc component and a small signal ac modulation,
1=10+i(t) we expect the optical output power to have corresponding dc and ac components (Fig. 11.1):
P(t) =Po+p(t) .>
In this chapter, we study the direct current modulation of diode lasers and som e intrinsic effects, such as relaxation oscillations, modulation speed, and the laser linewidth theory. Our goal is to understand how the laser light o utpu t characteristics vary as /we increase th e modulation frequ ency of the injection current.
11.1
RATE EQUATIONS 'AND LINEAR GAIN ANALYSIS
Assume that only one mode is lasing; then the rate equations for the carrier d en sity N (l/cm 3 ) and the photon density S O/cm 3 ) can be written as [1-4]
clN
cit clS dt _
]
N
q,{
T
._- - -- ._- :·, ('u( =' IV) ..{' J
- .r · c
S
'i/ ( •.
tV)) .-- .--- + f3 R sp
>...
( 11.1.1) (11 .1.2)
T{..
487
D]F.E:::T MODULATJO)\; 01~ SE.,liCONDUCTOR LAsERS
~P(t) = Po + pet)
pet) ......
~
o
0..
--8;:::l
P 0..
--
;:::l
o
Time :;> t
i(t)
Figure 11.1. For an injection current J = 10 + i(t), the optical output power is Pi t ) = Po + pet), where (10' Po) is the bias point for the direct current modulation of the semiconductor laser.
where
]
=
q
=
the injection current density (A I ern 2 ) a unit charge 0.6 X 10- 19 Coulomb)
d
=
the thickness of the active region (ern)
T
=
carrier lifetime (s)
L'
= c r n , is the group velocity of light (cm y s) .'
g(N) = the gain coefficient (l/cm)
r Tp
=
optical confinement factor
= photon lifetime (s)
f3 = the spontaneous emission factor
R s p = the spontaneous emission rate per .unit volume (ern -3 s-1) In the first rate equation (I1.1.1) for the carrier density N, the first term J Iqd is the injected number of carriers perunit volume per second. The current density} is the current I divided by rhe cross-section area of carrier injection. The recombination rate N
R( N) -
( 11.1.3) T
11.1
Rid E EOUATrONS AND LINEAR GAIN AI'iAL'(SIS
accounts for the carrier loss due to radiative and nonradiative recombinations. The time constant T generally depends on N, but is assumed to be a constant for simplicity. The term Lg(N)S is the carrier loss due to stimulated emISSIOns. In the second rate equation 01.1.2) for photon density S, the first term rL!g(N)S, is the increasing rate of the number of photons per unit volume due to stimulated emissions. The second term, - S / T p ' is the decreasing rate of the photon density due to absorptions and transmission through the mirrors of the laser cavity,
~
= L'
(a. + ~ln~J R
TIL p
(11.1.4)
where T p has the physical meaning of the average photon lifetime in the cavity. Photons disappear from the cavity via absorption processes or trans~~mission out of the end facets. The last term, {3R sp , is the fraction of spontaneous emission entering the lasing mode, which is generally very small. The spontaneous emission factor {3 can be calculated with a simple analytical expression for index-guided laser modes with a plane phase front (5]. For a gain-guided laser with a cylindrical constant phase front, the spontaneous emission is shown to be enhanced by another factor [6, 7]. It is noted [3] that the optical confinement factor r appears only in 01.1.2). This is because the optical mode extends beyond the active region d by the factor r. The two rate equations ensure that the total carrier and photon numbers are balanced taking into account the difference in the thicknesses (d versus d / I ).
11.1.1
Linea r Gain Theory
I f we assume that the photon density S is not high so that the nonlinear gain saturation effect can be ignored, we have a simplified gain model:
•
(11.1.5 )
where go = g( No), and g' = ()g IaN is the differential gam at N = No. Assume that 1 ( t) = 11)
+ j ( t)
'V( r) = NI;
+
s(r )
+
=
Sll
Il (
S(
where ii.t ) .'ti! J, n nd sl.i) a re small Sigll;tl~ mg dC"\'tdu.;;', III' til)" :F;·j 5'1)' l--:":;fJcctivcly.
t)
t)
l:()mp:~!;::d V.,:i(tl
( 11.1.6) their correspond-
DIRr::cr klODULATICIN OF SEMICONDUCTOR LASERS
490
de Solutions. The photon density So and the carrier density No at steady state are f3R:;p
50 = - - - - - ( 1 /1"p)
~ (:~
No
T
-
(11.1.7)
- r cs 0
(11.1.8)
LgoS o )
Note that for negligible f3R sp , the inverse photon lifetime is approximately 1 -
= fL'go
(11.1.9)
'T p
ac Analysis. The small-signal equations are
jet)
d
-net) dt
d -set) dt
=
=
- '-
qd
net) -
-- -
u[g'Son(t) + gos(t)]
(11.1.10)
'T
set) fv[g'Son(t) + gos(t)] - - ~
(11.1.11)
For a current injection with a microwave modulation angular frequency
(s)
(11.1.12) where jew) is the (complex) phasor of jet), we find the solution by substitutmg
net) = Re[n(w)e- i w t ] set)
Re[s(w) e-i(dt]
=
(11.1.13)
into (11.1.10) and (11.1.11). \Ve find the complex amplitude new) for the carrier density
n( (v)
I,
r-
reg So \
i co --
r ig () -+-
~Jlp.). s( w) (11.1.14)
where (11.1.9) has been u-:..~d. and the cornplex vnagnitude s(UJ) for the
photon density
s«({»)
fvg 'So[j(w)/qd] D( (v)
=
(J 1.1.15)
where the frequency dependent denominator Dt co) is
~
D(w)
iW( ~
- w' -
+
vg'So) + "g'::
(11.1.16)
Its magnitude square is
(11.1.17) Since the above function depends on w 2 , if we let y 2 occurs at (J/Jy)ID(w)1 = 0, we find
w; =
vg So
1_
1. ( 1 + ug'5 0 2 T
-
-
Tp
-
)2
2
= w ,
the mmimum
(11.1.18)
where the last term is usually negligible compared with the first term and
(11.].19)
is used. The relaxation frequency
I,
I,.
= wr /
27T
271 is
( 11.1.20)
A
which is proportional to or the square root of the optical output power since it is linearly proportional to the photon density 5 n . The frequency response function is s ( (u ~
I = .r I'.!? ' So / Wi
.i( w) I
! D ( (v) ! ( 11.1.2 L)
;::O Ir~ E · ..T rv'lnD~JLAT;O:~
-1-92
OF
5;::~''lICONDUCTOR LASERS
which has a fiat respon se at low frequencies 00\\/ pass) and peaks at co = W I" then rolls otT as the fr equency increases further. The bandwidth or 3-dB frequency I3dB (= W J lll3 / 2 7T) occurs at ID(W 3 d S >1 = or
n'w;,
(",juB since ID( (u
=
0)1
=
r '7
(Un' + wjdB (~
+
TpW; ~ 2 w;
(11 .1.22)
w;.
Example The frequency response for a distributed feedback semiconductor laser [8] is shown in Fig. 11.2 for different optical output powers at 5, 10, 15, and 20 mW. The peak respon se occurs at the relaxation oscillation frequency j,. and decreases to - 3 dB at f3dB compared with the normalized respons e at low frequencies (0 d B). T he bandwidth increases as the optical output power PI) increases with a ,;Po dependence, since PI) is proportional to the photon density So, as shown in Fig. 11.3. The 3-dB_!requency I3dB YS. the square root of the output power are shown with the relaxation frequency fro Since the output power Po is proportional to I - I t h , the plot, II" YS. ,; [ - I t h also shows a linear relationship. Therefore, II" can also be plotted vs. ';1 - I t h for semiconductor lasers and a linear relationship is shown [9]. Improvements of the modulation bandwidth using quantum wells and quantum wires or strained quan tum wells have been discussed [4, 10, 11]. l:II
M
12
.-
CD "0
W (J)
z
6
0
Q... (J)
W 0::
0
-
>U
z
w => a w
a:: u,
I
-
-
-
-
I I
--
I
-6
, I
-12
fr '::t 'oJ
I
l
lf3dB
I
1
6
9
FREQUE~jC '{
~2
15
is
(GHz)
Figure 11.2. Smul l s ignal f r·::l!u .:nl.:~ r ::"p01! S<:.' of a ci i:,l ,·i hu kJ fCI.' db 'ld·; luse r u t d ifle rcnt o u tp u t po v.. ers . Tile s ub rno u ru lclilPC::' ,lili r\.· \\ ,l ~, 21)"C'. Th e p'-',lk re s p o nse de te rm in es the rel axa ti on (re qu e ncy t,
4'·:3
20 r------r----.----,...----,.----
16 3 d8 BANDWIDTH-f 3 d8 N
I
~
12
>u z W
::J
o
w
8
0:
---- RELAXATION OSCILLATION FREQUENCY (fr)
LJ,..
4
OL-
o
'--
-'-2
1
.J.-
- ' - -_ _- - - - '
3
4
5
Figure 11.3. The relaxation oscillation frequency and the 3-dB bandwidth of the distributed feedback laser in Fig. 11.2 are plotted as a function of square root of output power P (or Po in the text). (Arter Ref. ~U
11.2 HIGH-SPEED l\;10DULATION HESPONSE \YITH NONLINEAR GAIN SATURATION [12, 13] 11.2.1
Nonlinear Gain Saturation
The gain model g(N) can be taken from ( 11.2.1) where ,go = g(No), s' = (C>g IaN ),v=No IS the differential gam at NI). The factor '1 + ES accounts for nonlinear gain saturation, which is important when the photon density is high. The factor E is called the gain suppression coefficient. The steady-state solution at 1 = 10 is obtained from did t = 0 in the rate equations: JI)
NI)
qd )
8iJ'
-; (I
1' I' ------.-. 1. +1::,)'11
L"'Y ,:.1) S ()
+
-
._.~--
1
T
Sp ..
_-
eo .> \
I
Tp
~
T
l
:'l
( 11.2.2)
PSI' . j
~"I
(
')
1 1..... .J
,.-"
)
" .
."
.,.
~
~_~
"'";"1 '\
~
• • "'""t••
~'" .,
.. tr,;,,-r-::-:'- -
. ' f. ~~" ·~ _
I.JJ I~LC ; ' ~,·C(y)U :..i \T IO N
494
:1·'
,...,.. . ....
..
OF SE .:MCONDUCTOR LASERS
If e =F O~ the general solution of (11.2.3) is
~ r- (~"» - r
5o = 2
e
cg 0 - e (3 R Sf) )
and No is obtained from (11.2.2) using the above 50' Using the linearized expression by substituting (11.1.6) into (11.2.1), we obtain
g(N)
go 1 + £5
=
0
g'n(t) + 1 + e5
( 11.2.5) 0
The ac responses ni t') and s( t) satisfy the following equations: d dt
-net)
jet) net) -d - - - -
=
q
T
[U g '5 0 1
+ £So
1net)
ug o
-
(1
+ cS c.
)2 S
( t ) (11.2.6)
O
and
~s(t) dt
=
(
fug'So ]n(t) 1+E5 0
+
set)
..,s(t) (l+eSof fuga
which can be derived by keeping :the first-order terms of n( t (11.1.1) and (11.1.2) and using 01.2.5). 11.2.2
)
(11.2.7)
and st.t ) in
Sinusoidal Steady-State Solution of the Small-Signal Equations
Using d/dt
~
- iw in 01.2.7) and 01.2.3), we relate s to n
.
-lw(1 + £5 0 [
! +.
E5 0 f3 R sp ] --;; + ~ s( w)
.
=
(fLIg'5 o) n( w)
(11.2.8)
'rYe then use (11.2.6) and find 1
(
-r,
- i w + _.T
cg'5 o I)
+ - - --, tl ( w ) _. 1 + c') o ,
j( (u ) qr.!
vs;
-(---~S'/ s( w) (lJ .2.9) 1+ e
or
· i .2
N )NLINEAR (J /d"r SATUIU\TJON
4';5
Therefore, the small signal photon density function is
s( (1.»)
Define (11.2 .11 )
which is the same as 01.] .19). We obtain the frequency response function for semiconductor lasers 2
s( W) j( W)
(1].2.12)
where a damping factor 'Y is defined:
= rg'
So(1 +
= Kf} +
_ 8-
ug'rr;
J+
1 T
1
(11.2.13) T
Here a K factor (ns) K
=
47T
2
(T!~
-+
~-) rg '
(11.2.14)
I
and W r = 2 »I, have been used. The 3-d B cutoff frequency occurs ,H ( 11.2.15)
S~~MICC·NDUCTORLASERS
DIRECt tvIOijL)rj'\TIO>1 OF
The maximum possible bandwidth occurs when the following condition is satisfied:
(11.2.16) such that the frequcncy response function is a monotonic decreasing function, (11.2.12) a W;/((tJ4 + w;). We then have the maximum relaxation frequency by solving 01.2.16) for I,.: 27Tfi j~,lllax =
(11.2.17)
K
By fitting the frequency response function 01.2.12) to the experimental data, the damping factor y can be found together with the relaxation frequency L. Equation (11.2.13), y = Kj} + 1/ 'T, shows that a linear relation with a slope K holds if the damping factor 'Y is plotted vs. j} and the intercept with the vertical axis gives the inverse carrier lifetime 1/ 'T . Example Figure 11.4 shows the experimental results [14] for two strained quantum-well lasers with (1) a slope K = 0.22 ns for a tensile strain laser with four quantum wells, and a maximum bandwidth j~. max = 27Tfi / K = 40 GHz, and (2) a slope with K = 0.58 ns for a compressive strain laser with four quantum wells and fro max = 15 GHz. Both lines intercept the vertical axis at 1/ 'T ::::::: 5 GHz, and the carrier lifetime Tat threshold is 0.2 ns for both 40
,--------~---------~-~----.
t
--. N
I
30
<.9 '-'" ;=-
20 • 4 MOW tensile strain K = 0.22, l ma x ::; 40 GHz o 4 MQW compressive strain K = 0.58, 'max = 15 GHz
10
o '"o
.L..-.-.
20
.L..-.-._ _ .------JL--.-_
40
60
_----..J
80
-.J
100
(1 (GHz 2 ) r igur e 1l...l. and
1/'
Experimented results ,huwing rh,C' li.ic ar relation between the damping factor 'Y
for two quantum-well Lt~t:J::;, 'Y = f\f,~ -l- liT. The slope: g:"/cs the: K factor (in ns) an d
the: intercept with the y axis gives the inverse cl:'ri::l" liL:tinlC J /T at threshold. (After Rd. 1-.1-.)
IU
SE MICUN D UCT O R Lt\S[.R S;'LCTRAL Ul'IEWlDTH
samples. The difference of the slopes of the two laser structures can be explain ed fr om the differen ce in the differential gain of over a factor of 2, sin ce J} /P o = 3,6 GH z 2/ mvY for the compressive strain la ser and f } jPo = 7.7 GHz 2/ mvV for the tensile strain sample. Ii]
Since the damping f actor depends on th e K factor, relaxation frequency , a n d the inverse carrier lifetime, the experimental data provide very good guidance for the design of high-speed semiconductor lasers . The K factor, K = 41T 2 ( 'T{I + (e/vg'» , can also be used to determine the nonlinear gain suppression coefficient E. Theoretical models and experimental data on strained and unstr airied quantum-well lasers have been presented with interesting results [15-24]' T h e measured nonlinear gain suppression coefficient E ranges from 2 to 13 X 10 - 17 cm ' for InGaAs or InGaAsP materials in the quantum wells [15, 17, 18]. V arious physical mechanisms such as the well-barrier hole burning effects [20], carrier heating and spectral hole burning [21], carrier transport [22, 231, and carrier capture by and e scape from quantum well s [25-27] have been investigated and-shown to affect by varying degrees the high-speed modulation of semiconductor quantum-well lasers. More work is in progress to understand the ultimate limit on the high-speed modulation of semiconductor lasers.
11.3 SElVIlCONDUCTOR LASER SPECTRAL LINEWlDTH AND THE LINEWIDTH ENHANCEMENT FACTOR The spectral properties of semiconductor lasers have been investigated since the early 1980 s. Experiments by Fleming and Mooradian [28] showed that the laser s p ec t ra l linewidth has a Lorentzian shape and the linewidth is inversely .p ro p o rt io n a l to the o p t ica l output power. However, the magnitude of the .linewid t h wa s much larger than they had expected from conventional theories. A m odel proposed b y Henry [29, 30J explained the phenomena by noting th at the se mico nd u cto r la ser is similar to a detune.d o scillator, a n d th ere is a sp ec t r um linewidt h e nh a nce me n t due to the coupling betwe en the amplitud e a nd phase fl uctua t io ns of the optical field . A linewidth enhancement factor 0'<, is introduced
a
() n'jrJ N =
"
_ . ~~
un "j aN
( 11.3 .1)
a nd th e la se r Iin e w idth h as a b roud e nin g enhan cement by an a mo u n t 1 + a ~ . H e re /1 ' nn e! II " a re th e re al and imaginary par ts of the refractive ind ex du e to the ca rr ier injec tio n int o th e active re gio n and N is t he ca rr ie r density, A
more form a l d eri vati o n h ~I S bee u give n by Va hJh and Yar iv [J 11. In this sec tio n, we prese n t th e m udel of Henry.
·198
DIR ECT tv :ODl: .U \ T l , )N O F S Ei'dl CON[ >U ClOR LASERS
11.3.1 Basic E qua tio ns for th e Optical In t ensity and. Phase in the Presence of S po n ta neous Emiss ion
Consider an o p t ica l field F-:; ( z , t ) give n by
E( z ,t) = E ( t ) e ilkz -w, ) E( t) -
(11.3.2)
(i(iT e i .pl l )
(11.3.3)
where [Ct) represents the intensity and ¢(t) th e phase of laser field. We assume [Ct) = E(t)E*Ct) has been normalized such that it represents the average number of photons in the cavity. The time-depend ent magnitude Ei t' ) is a complex phasor , assuming that its time va r ia tion is much slower than the optical fr equ en cy UJ. The phasor E Ct ) is plotted in the complex plane as a vecto r with a magnitude fi(t) a nd a phase ¢ (t) , as s ho wn in Fig . 11.5. The basic assumption is that a random spo n ta ne o us emission alters Ei t ) by /1 E , which adds a unit magnitude (one photon) and a ph a se e, which is random : .
-
...
(11.3.4)
There a re two co n tribu tio ns to th e ph ase change /1¢ :
(11.3.5) wh ere /1¢ ' is du e to the out-of-phase component of /1E , and /14>" is due to th e intensity chan ge which is coupled to the phase change . T o obtain the first contribution, /14> ', we note from Fig. 11.5, that 11 /1¢' ::= sin 8, or sin 8
(11.3 .6)
11 Irn E (t)
"
_~_--t.
F igure J 1.5 .
--::> Re E (t)
A pl o t o n til e co m p le x o p tica l c k,': ric he ll! [:29] EU) ~'"
/f(lT e:w li(p U )J d om ain
s how ing that its m a gn itu d e ..;7 a nd p hase :/) c.ui k : c ha nge d by th e s po n ta ne o us em iss io n of a p ho ton ( mag n itu d e is o ne si nce (he in te nsity ( iu s b ~: e n norma lize d to rep re se nt th e ph oton n umb er i ll the c.ivity) with a p h.rse ch :lIlge j, ,!,' . .
'11.-'
SEM ICONDUCTOP. LASER SPECTRAL L rI';EWID~~H
To obtain the second contribution, 6¢", due to the intensity change, we start from the wave equation 1 a2 2" -2 E,.£(Z, t) c at
where c is speed of light in free space and .», E,. = e j £0 of the semiconductor. We obtain
BE(t)
2iw
-£
c2
= -
at
r
2 (W- E c2
r
-
( 11.3.7)
the relative permittivity
IS
)
k 2 E(t)
( 11.3.8)
neglecting the term B2 Ei t ) jBt 2, since E(t) is a slowly varying function. We can also express Erin terms of the complex refractive index ~
VEr
I
= n
+
(11.3.9)
."
In
and
co
-ji; c
=
k=
w
w
c
c 1
-n' + i-n" co ,
co
-(g - a) 2
-ll
C
--n" c
( 11.3.10)
where g is the gain coefficient, and a is the absorption coefficient of the optical intensity. At threshold, the gain is balanced by the absorption, (g = a), n" = 0, and e , is real. Changes in carrier density N will cause n' and nil to deviate from the threshold values: E,. =
n'
(
= n ,/-
+
A' ts n
+ 2'In
r
+ lun . ")2 A
A "( 1 un
. ) la e
(11.3.11)
where we have defined a linewidth enhancement factor a e as the ratio of the change in the real part of the refractive index to the change in the imaginary part: .1n' at' =
.1 nil
( 1.1.3.12)
Therefore
DE (it .. (;
( ,
'-- 't -,
~~~-
-
) I' (j ,
.- i a ., ) E'(I )
\"l~l") J ..) . .)
f " -::- --C;- ' ~"'I":'
__ ~ .~--: .~",,-.,.,<".,, '_ .•.• ~.-r ....• - .._ . - ..-
. , or" -
..... . . .
500
~,
-':
"'....
,.~'
~
"
_.- "
-
-,,-
-
DIRE CT rviOD Ui A T IU!':
.,'
-
O~:
••.
_
• _
, _ . ..
"
, ..
.'
.... ..
,. ~ '"
'..
t
~
SEMICONDUCTOR LASERS
where the group velocity L: = C / u' has been used , and we ignore th e dispersion effect for simplicity. If we include the effect of the material dispersion , (11.3.8) has to be modifi ed [29J and the result fo r 01.3.13) still holds with the group velocity given by u = cj(n' + W on' jo(u), which is derived usin g k = (UlZ'je and lJ = (okjaw) -l. Substituting E(t) = fi(i)-eirJ>(t) into (11.3.13) and separating the real and imaginary parts, we find 1 dl
- ( 2 dt d¢ -
dt
-
-
g - O' )
2
vI
( 11. 3 .14a )
(g-2 a)
(11.3 .14b)
[)O'e
Therefore, we obtain d¢
2/
dt
(11.3.15)
dt
Initially at t = 0, 1(0) = I + 6.1, and at t die out, 1(00) = 1, and we obtain
=
co ,
the relaxation oscillations
a 6.¢" = .': 6./
21 O'e
2 / (1
rr
+ 2y /
cos 8)
(11.3.16)
which can be derived from the relation among the three s id e s of the triangle in Fig. 11.5. The total phase change is then 6,
«.
= -
2/
+
6.¢"
+
IT/ (sin e + a
1
e
cos 8)
(11.3.17)
The ensembl e average of the spontaneous emission events at a time duration t is contributed from the constant term ( O'ej2 I) multiplied by the total number of the events , R spt:
( 11.3.18) since <s in &) = ( cos () > = O. H ere R "p is the spontaneous e m ISSlOn rate (l js). Equati on ( 1 1.3.18) gi \ e ~ an a ng u lar fr equency s h ift: rl '-
6!u = -- <6(b ) df '
=
a" - H. '2 J sp
( LJ.3.19)
l Jl .•.,~
SE;
lll~ONDUCTOR
,:-,Ot
LASER Sr::,CTRAL LU-':EWIDTH
The total phase fluctuation for Rspt spontaneous events gives the variance:
(11.3.20)
We use an absolute value for It I since (6.4>2) is a positive quantity. Therefore, we found the mean (6.4> > and its variance (~4>2 > as above. 11.3.2
Power Spectrum and Semiconductor Laser Spectral Linewidth
The power spectrum of the laser is the Fourier transform of the correlation function:
YV( w)
f
co
d t ei
(v
E *( t ) E ( 0) >--
t(
-oc,
_ foo
dt
e iw t (
[1( t ) I ( O) r / 2
e-ic.(t»
-cc
:::::: 1(0)
foo
dt
eiwt(e-i..l>U)
(11.3.21)
-00
where the small intensity fluctuation is neglected and the amplitude function for the field E(l) = [1(t)]1/2 eiJ>(t) has been used, which does not include the central frequency of the laser, that is, w in (11.3.2), and .'
~4>(t) =
4>( t) - 4>(0)
Since the spontaneous emission events are random, the phase ¢ should have a Gaussian probability distribution function, P(~cP) = a Gaussian function. The ensemble average for a Gaussian distribution is [30, 32] (e-i..l(t»
=
IX d(D..(/.»P(~(p)
e-i..l,/,
-COL
( 11.3.22) Using the result for the variance <::'.(//')
LI1
(11.3.:20), we can define a
coherence time as 1.LL"~ I l {'
)
- -----!\ 41 'i'
( 11 .J .2J )
•
SU2
such that function
DJRi:C'T MODULATlON OF SErvllCONDUCTOR LASERS
<6.cP 2 ) /2
=
It 1/ t The power spectrum (] 1.3.21) gives a Lorentzian C'
(11.3.24 ) with a full width at half-maximum (FWHM) of Dow =
2 _ (1 + a;) R t 21 sp c
or
Do! =
(1 +
an
4TT" 1
R
(11.3.25)
(11.3.26)
The number of photons 1 in the laser cavity (the photon density multiplied by the volume) is related to the optical output power by (I0.1.28)
( 11.3.27) where Ifzw is the total photon energy and va m is the escaping rate of the photon out of the cavity with a length L, where a
rn
1 L
1 R
= -In-
(11.3.28)
and R is the mirror reflectivity at both ends. We find !1f=
(11.3.29) I
which are commonly used 'to explain the spectral linewidth of semiconductor lasers. Alternatively, the spontaneous emission rate (l/s) is related to the gain coefficient (I / cm ), by a dimensionless spontaneous emission factor n~p:
R sp
= ugn
sp
(11.3.30)
where 1
(11.3.31) and t:..F = Fe - F; is the separation of the quasi-Fermi levels between the electron and the hole. Note that the photon number 1 and the spontaneous
ermss io n rate R ~p (l Is) are defined for the whole volume of the active region.
11.3.3
Linewidth Enhancement Factor in Semiconductor Lasers
Experimental data [33] for the laser linewidth 6./ depending on the op tical output power with an inverse law are shown in Fig. 11.6. The surprisingly large linewidth measured in this set of data was explained by Henry [29] using the correction factor (l + a ~), where a e = S. More measurements have been done for various semiconductor lasers including index-guided double-heterostructure, unstrained and strained quantum-well lasers, with reduced linewidth enhancement factor [34, 35] a e . In a semiconductor laser, the injected carrier-ind uced refractive index change is associated with the change in the gain. The linewidth enhancement factor a t can be directly expressed in terms of the differential change of the refractive index per injected carrier vs. the differential gain: dn' ae =
-
200
eln"
47T dn/dN
--
(11.3.32)
A dg/dN
r----,----.---r-""'T'"--r--T----,r--~-_..........
160 .' N
:r
~
120
:z:
~
Cl
~
w
80
Z ..J
SLOPE a 9.28 77 K
40
o
0.3
lNVERSE }<":g Ui' L'
1.1. O,
Se m ico nd uctor
1.~
1.0
PO "HER
L ~ :< f lil,!<:v,idtil ';eiSUS
Z.O
z.~
1 {mW- }
invc rse power
at
three temperatu res ex hib it-
in g. the lin ear beh av ior . ( A l' tc i Ref. 33.) The magn itudc of the lari,:c lincwidth was explain ed [29] ll si r~g th e co rrec tion fucior 1' -1- (t :: with ry, == 5 ut r(Joln temperature.
. ~
-:'
-H-''''r ,.,....
.,"'
~
,
•.
.-~ ... ~.
---
'..
.
12 . - - - - - - - - -
't
l;j'D
10
'-
o
u ~
8-
" 4 MOW tensile strain (In O.3Ga 0.7 As)
o 4 MOW compressive strain (Ino,eGao.2 As)
6
4 2 O'------"'-------....L.---_-...JL-.1400 1450 1500 1550 Wavelength (nm)
----.J
1600
~
Figure 11.7. The linewidth enhancement factor LYe vs. wavelength of two types of strained MQW lasers. The lasing wavelength is indicated by the arrows. (After Ref. 14.)
where we have used dn"/dN = (-1/2)(dg/dN)/(21T/A) in 01.3.10) with w / c = 274/ A, and A as the wavelength in free space. The linewidth enhancement factor varies from about 1.5 to 10 and is dependent on the lasing wavelength. Experimental data of Q'e for two strained quantum-well lasers are shown in Fig. 11.7. The high-speed modulation characteristics of these lasers are shown in Fig. 11.4. The dependence of CI.' <: on the loss or the Fermi levels of semiconductor lasers has also been shown to be important [36]. For strained quantum wells, theoretical analysis [37] shows that Q'e can be reduced to about 1.1 using tensile strains with TM polarization of semiconductor quantum-well lasers. Similar behavior to the spectral broadening in semiconductor lasers also occurs in an intensity modulator using the e lectroabsorption effects [38-40]. This is because a phase modulation due to the change in the refractive index is associated with the change in the absorption coefficient. PROBLEMS 11.1
11.2
Estimate the photon lifetime for a semiconductor laser assuming the following parameters: CY i = 10 cm- 1, refractive index = 3.2, and, cavity Ie ngth L = 200 ,u m. Discuss the effects on photon lifetime if we increase the cavity length or reflectivity by a factor of two. Derive (a) the de solutions for So arid No and (b) the ac solutions for s( t ) and nt; [) in the linear gu in tl! - ory .
•
11.3
.. .,~
Discuss how Olle rnuy improve the relaxation frequency semiconductor laser.
I,.
of a
RLFER Ei\iCES
50)
I 1.4
Derive an expression for the 3-dB angular frequency W 3d B for the small signal frequency response of a semiconductor laser using the linear gain theory.
11.5
Derive the de solutions for So and N u in the nonlinear gain theory for the frequency response of a semiconductor laser.
11.6
Derive the ac solutions for si t) and nCr) in the nonlinear gain theory.
11.7
Discuss the effect of decreasing the damping factor 1'.
11.8
Plot the frequency response curve when the condition 2w~ = 1'2 satisfied.
11.9
Derive 01.2.13) and discuss the approximations used.
11.10
IS
Derive 01.3.13) and 01.3.14) taking into account the material disperSIOn.
11.11
Derive (11.322) for a Gaussian distribution function P(t::.¢).
11.12
Describe the factors determining the spectral linewidth of a semiconductor laser. How may one decrease the semiconductor laser linewidth?
REFERENCES 1. T. Ikegarni and Y. Sue matsu, "Resonance-like characteristics of the direct modu-
lation of a junction laser," Proc. IEEE 55, 122-123 (1967).
2. A. Yariv, Quantum Electronics, 3d ed., Wiley, New York, 1989. 3. K. Lau and A. Yariv, "High-frequency current modulation of semiconductor lasers." Chapter 2, in W. T. Tsang. Vol. Ed., Lightwai:e Communications Technology. Vol. 22, Part B. in R. K. Willardson and A. C. Beer, Eds., Semiconductors and Sernimetals, Academic, New York, 1985. 4. K. Y. Lau, "Ultralow threshold quantum well lasers," Chapter 4, and "Dynamics of quantum well lasers," Chapter 5, in P. S. Zory, Jr., Ed., Quantum Well Lasers, Academic, San Diego. 1993.
). T. P. Lee, C. A. Burrus, J. A. Copeland, A. G. De ntai, and D. Marcuse, "Short-cavity InGaAsP injection lasers: Dependence of mode spectra and singlelongitudinal-mode power on cavity length," IEEE 1. Quantum Electron. QE-18, 1101-1112 (1982). 6. K. Petermann, "Calculated spontaneous emission factor for double-heterostructure injection lasers with guiu-induced w.ivc guiding,' IEEl:-' J. QW/J1twn Electron. QE-15. 560-570 (1 (79). 7. W. St rcifer, D. R. Scifres, and R. D. Bu r ah.rm. "Spontaneous emission factor of nurrow-suip gain-guided di,)(\t' lasers.' Elntron . Lett. 17. 933 (l9R I).
,\ N. K. ouu., S. J. \Vang. ,\. B. Piccirilli. r: F. Karlicck, J1' .. R. L. Brown, M. Washington, U. K.. Ch;I:,rt;llJit~. aile! ,-\.. Gua uck.: "Wide-bandwidth and
DIR:cCf MO)'ULAi I{)N OF SF MICONDUCTOR LASERS
506
high-power InGaAsP distributed feedback lasers," 1. Appl. Phys. 66, 4640-4644 (1989). 9. K.
Uomi,
M.
Aoki, T.
Tsuchiya,
and A.
Takai,
"Dependence
of high-speed
properties on the number of quantum wells in 1.55 fLm InGaAs-InGaAsP MQW A/4-shifted DFB lasers," IEEE.I. QuailtLilIl Electron. 29, 355-360 (1993). LO. Y. Arakawa, K. Vahala, A. Yariv, and K. Lau, "Enhanced modulation bandwidth
of GaAJAs double heterostructure lasers in high magnetic fields: Dynamic re
sponse with quantum wire effects," Appl. Phys. Lctt. 47, 1142-1144 (1985). 11. Y. Arakawa and A. Yariv, "Quantum well lasers: gain, spectra, dynamics," IEEE
1. Quantum Electron. QE-22, 1887-1899 (1986). 12. R. Olshansky, P. Hill, V. Lanzisera, and W. Powazinik, "Frequency response of 1.3 fLm InGaAsP high speed semiconductor lasers," IEEE 1. Quantum Electroll.
QE-23, 1410-1418 (1987). 13. R. Olshansky, P. Hill, V. Lanzisera, and W. Powazinik, "Universal relationship between resonant frequency and damping rate of 1.3 fLm InGaAsP semiconductor lasers," Appl. Phys. Lett. 50, 653-655 (1987).
14. L. F. Tiemeijer, P. J. A. Thijs, P. J. de Waard, J. J. M. Binsma, and T. V. Dongen, "Dependence of polarization, gain, linewidth enhancement factor, and K factor on
the
sign
of the
strain
of
InGaAs / InP
strained-layer multiquantum
well
lasers," Appl. Phys. Lett. 58, 2738-2740 (199l). IS. T. Fukushima, J. E. Bowers, R. A. Logan, T. Tanbun-Ek, and H. Temkin, "Effect of strain on the resonant frequency and damping factor in InGaAs / InP multiple
quantum well lasers," Appl. Phys. Lett. 58. 1244-1246 (1991). 16. S. D. Offsey, W. J. Schaff, L. F. Lester, L. F. Eastman, and S. K. McKernan, "Strained-layer InGaAs-GaAs-AIGaAs lasers grown by molecular beam epitaxy for high-speed modulation," IEEE J. Quantum Electron. 27,1455-1462 (1991). 17. H. Yasaka, K. Takahata, N. Yamamoto, and M. Naganuma, "Gain saturation coefficients of strained-layer multiple quantum-well distributed feedback lasers,"
IEEE Photoll. Techllol. Lett. 3, 879-882 (991). 18. -J. Zhou, N. Park, J. W. Dawson, K. Vahala, M. A. Newkirk, U. Koren, and B. I.
,
Miller,
"Highly nOl1lkgenerate four-wave
mixing and
gain
nonlinearity in
a
strained multiple-quantum-wcll optical amplifier," Appl. Phys. Lett. 62,2301-2303 (1993).
19. S. R. Chinn, "Measurement of nonlinear gain suppression and four-wave mixing in quantum well lasers." Appl. Phys. Lett. 59, 1673-1675 (l99JJ. 20. W.
Rideout,
W.
F.
Shlrfin,
E.
S.
Koteles,
M.
O.
Vassell,
and
B.
Elman,
"Well-barrier hole burning in quantum well lasers," IEEE Photon. Technol. Lett. 3. 784-786 (1991).
21. A.
Uskov, J.
Mork,
and J.
Mark.
"Theory of short-pulse gain saturation
in
semiconductor laser amplifiers," IEEE Photo/l. Tpchllol. Lett. 4, 443-446 (1992). "
R. Nagarajan, T. Fuku:)hirnd, S. 'vV. Corzine, aDd J. E. Bo\vcrs, "Effects of carrier transport on high-speed C]ucntum \Veil lasers," Appl. Phys. Lett. 59, 1835-1837 (j 9(1).
23. A. P. 'Wright, B. Garrett. G. H. B. ThD:np.,,"', :1lld J. E. A. \Vhitemvay, "Influence of carrier transport un \\-:,',ckf1gth chi;'p (ft" InCi'-t/\s/InC:T:'lJ-'\sP MQ\V lasers," Electroll. LeU. 23,1911-1913 iL9(2).
sm 24. E. Meland , R. Holmstrom, J. Schlafer, R. B. Lauer, and W. Powazinik, " E xtremely high-frequency (24 Gl-Iz) InGaAsP diode lasers with excellent modulation efficiency," Electron. Lett. 26, 1827--1829 (1990). 25. P. VY. M. Blom , J. E. M. Haverkort, P. J. van Hall, and J. H. Wolter, " Ca r d e r - carrie r scattering induced capture in quantum-well lasers," Appl, Phys. Leu . 62, 1490-1492 (1993). 26 . D . Morris, B. Devcaud , A . Regreny, and P. Auvray, "Electron and hole capture in multiple-quantum-well structures," Phys. ReI.'. B 47 , 6819-6822 (1993). 27. S. C. Kan, D. Vassilovski, T. C. Wu , and K. Y . Lau, "Quantum capture limited modulation bandwidth of quantum well , wire, and dot lasers," Appl, Phys. Lett. 62,2307-2309 (1993). 28. M . W. Fleming and A . Mooradian, "Fundamental line broadening of single-mode (GaAl)As diode lasers," Appl. Phys. Lett. 38, 511 (1981). 29 . C. H. Henry, "Theory of the linewidth of semiconductor lasers," IEEE J. Quantum Electron. QE-18, 259-264 (1982). 30 . c. H. Henry, "Spectral properties of semiconductor lasers," Chapter 3, in W. T. Tsang , Vol. Ed., Lightwave Communications Technology, Vol. 22, Part B, in R. K. Willardson and A. C. Beers, Eds., Semiconductors and Semimetals, Academic, New York, 1985. 31. K. Vahala and A . Yariv, "Semiclassical theory of semiconductor lasers, Part I," IEEE J. Quantum Electron. QE-19, 1096-1101 (1983). 32. M. Lax, "Classical noise, V, Noise in self-sustained oscillators," Phys . Rev. 160 , 290-307 (1967). 33. D. Welford and A. Mooradian, "Output power and temperature dependence of the linewidth of single-frequency cw (GaAl)As diode lasers," Appl. Phys . Lett. 40, 865 -867 (1982). 34 . Y. Asai , J. Ohya, and M. Ogura, "Spectral lincwidth and resonant frequency characteristics of 1nGaAsP/ 1nP multiquantum well lasers," IEEE J. Quantum Electron. 25, 662-667 (J 989). .' 35. N. K. Dutta, H . Temkin, T. Tanblln-Ek, and R. Logan, "Linewidth enhancement factor for In GaAs Z Inf' strained quantum well lasers," : Appl. Pliys. Lett. 57, 1390-1391 (1990). 36 . Y. Arakawa and A. Yariv, "Fermi energy dependence of linewidth enhancement factor of GaAIAs buried heterostructure lasers," Appl. Pliys. Leu . 47, 905-907 ( 1985)'37 . Y. Huang. S. Arai , and K. Komori, " T heo re tica lI inew id th enhancement factor of Ga I _. .. In .,.As / GaInAsP/ InP strained-quantum-well structures," IEEE Photon. Tee/fllUt . L eu . 5, 142-145 (1993). 3':-:. F. Koyama and K. 19a, "Frequency chirping of external modulation and its reduction ," Ele ctron. Lett . 2l, 1065-1066 (985) . .N . Y. Noda, M. Suzuki, Y. Kushiro, and S. Akiba, " H igh-s p ee d e lectroab sorption m odulat o r with st r ip -lo ad e d Ga InAsP planar waveguid e ," 1. Lightwtu:e Tcchnol . L:r-.:L l445-l453 (l986). 4(). 1". 1-1. \Vood . •. Multiple quantum well (MO\,V) waveguid e modulators ," J . Li ghtH '(/ CC Tcchnol. 6 , nJ --757 ([':HS).
12 Electrooptic and Acoustooptic Modulators In this chapter, we discuss eleetrooptic effects and modulators. The bulk electrooptic effects are di scussed first, and their applications as amplitude and phase modulators are presented. These devices using waveguide structures are then shown . The basic idea is that the optical refractive index of electrooptic materia Is, such as LiNbO 3' KH 2 P0 4 , or GaAs, and ZnS semiconductors, can be changed by an applied electric field. Therefore, an incident optical field propagating through the crystal with a proper polarization experiences efficient electrooptic effects. The transmitted field changes in either phase or polarization, which can be used in the designs of phase modulators as well as amplitude modulators. We then discuss scattering of light by sound and present a coupled-mode analysis for acoustooptic rncdulators.
12.1 ELECTROOPTIC EFFECTS AND AMPLITUDE MODULATORS [1, 2] To understand the e lectrooptic effects, we consider a crystal described by the constitutive relation associating the displacement vector D to the electric field E by a permittivity tensor E.
(]2 .1.1)
arid the permeabllity tensor € as K:
IS
fLo.
Let us define [he Inverse of the permittivity
K
The index ellipsoid
I~) Y
==
£--1
(12.1.2)
th e cryvt al is descritcd by c, c.
\"'
L'
\-
'"
U ~ !\. i I ~ t·l...'
Ii
c'"
(12.l.3)
12. )
dJ::CTR002T1C L fFEC"T:-; ;\i',Jj t\l\fPU rUDE
i'vIODULAT\)R.~
~09
where Xl = x, J 2 = y, and x 3 = z for convenience. For most crystals, E is symmetric due to the symmetry property of the structure. Therefore, ~ can be cliagonalized to be
= £=
[
E~'
0
(12.1.4)
E }'
0 The coordinate system iIL which £ is diagonalized is called the principal system. In this system, EoK is a diagonal matrix with the diagonal elements equal to the reciprocals of the square of the refractive indices of t he three characteristic polarizations along the direction of the principal axes:
EoK = EO
l/Er
0
0
2 1/n . x
0
0
0
l/E y
0
0
l/n;,
0
0
0
l/E z
0
0
1/11;
(12.1.5)
and the index ellipsoid (12.1.3) is
1 -+-+-Xl7
E
where I'li 12.1.1
=
o ( Ex
y2
')
Xi?
x-
EyE z
n~
Xi7
7
+
n 2y
'1
Z'-
+
fl~
1
( 12.1.6)
I~i/Eo' i = x, y, and z.
Electrooptic Effects
In a linear clcctrooptic material, the index ellipsoid is changed in the presence of an applied electric field F, and K i j becomes K i j + 11 K i } , where the change 11 K i j is linearly proportional to the electric field: 3
Eu
11K,}
=
L
rij k
r,
(12.1.7)
k=J
The linear electrooptic effect is also called the Pockels effect, after. Friedrich Pockels (3] 0865-1913), who described it in 1893. These r i j k coefficients are also called Pockels coefficients. Equation (12.1.7) can also be generalized to include the quadratic e icctrooptic effects. which are usually smaller than the linear effects, -' r) l ~ ' . . cJ ll .:..
EL ECTRO(..?TlC I\ ND :\COUSTOOPTIC
510
MODULATOR~;
However, for materials with centrosvmrn ctry, the index ellipsoid function mu st be an even funct ion of th e applied el ectric field, since it must remain invariant upon the sign reversal of the el ectric field. Therefore, r i j /.; vanishes and the quadratic e1cctrooptic effects dominate. The quadratic ele ctrooptic effect is also called the Kerr effect , after John Kerr [3] (1824-1907), who di scovered the effe ct in 1875. From the symmetry property of the crystal, the following matrix correspondence is defined:
(1 2.1.9)
that is, we have (ij) ~ 1 = 1,2, ... ,6, and ri jl<. = rj i k == r fl" Note that r1k 6 X 3 matrix, and Eq. 02.1.7) can b e rewritten as
to
(~K)]
r
(6.K)z
' 21
(6.K)3
r31
(6.K)4 (6.K) s (6.K )1)
Ii
I'll.
'13
r 33
'41
rn r 32 r42
r5 1
1'5'2
r 53
r6 ]
r 62
r63
" 2J
'"43
[;: ]
IS
a
( 12.1.10)
Depending on the symmetry of the crystal, many of the matrix elements r 1k m ay vanish. We usually refer to some databook [4] or reference tables [5-8] for the crystal symmetry and nonvanishing rJk va lues. A few important electrooptic materials are shown in Table] 2.1, for illustration purposes.
Example The potassium dihydrogen phosphate (KO P or KH 7 PO,) crystal is uniaxial in the absence of an applied field : ...
7
X.:. EO
L « >», IJ
n 20
z-J
y-
-+-
.,
Il ~
+
n J2
1
(12.1.11)
where n .r = Il~. = no' and n z = 11 c : With an applied field, we have r 1k = 0 except for r6J 'and "41 = r 52 · Therefore, Eq. 02.1.10) gives Eo(6.K)4 = r-lIF] , 1;'o( t1 K )) = r 52F2 , and EI)(6.K) t, = r cJ:;F:,. Note that Xl = X, x 2 = y, x J = z , a nd lise the mapping table in ( I? . J ,9 ):
cu :L 1K
i j ' \ i .t"j
= 2i .l i F, v; +-
21':'>2
F\..\.:: + 2 rl ) F
yx
_
'") ') (1 7 .1..1.:-
iJ
wh ere a fa ct o r 2 acco unts for t he syrnme rr ic property of th e matrix il K i j ,
In general, the above index ellipsoid may not have the principal axes along the x, Y, or z directions any more, as will be shown in the following examples. III 12.1.2
Longitudinal Amplitude Modulator
Consider the setup as in Fig. 12.1 with the applied electric field along the propagation direction (z ) of light F = iF_. The index ellipsoid is
1
(12.1.14)
The above equation shows that the principal axes along the x and y directions are rotated because of the cross term , 2r6 3 F;: xy . \Ye have to find Table 12.1
A Few Electrooptic Materials 'With Their Parameters [1,4, 6, 9]
Refractive Index
Point-Group Symmetry
Materi al
no
3m
Li.Nb0 3
2.297
Wavelength Ao(j.Lm)
Ill!
2.208
0.633
Nonzero Electrcoptic Coefficients (10 -12 m/V) "D r~2
1'12
32
Quartz (Si0 2 )
1.544
1.553
0.589
42m
KI-I 2 POol (KDP)
1.5115 1.5074 1.5266 1.5220 1.5079
1.4698 1.4669 J .480 8 1.4773 ] .4683
0.546 0.633 0.5'+6 0.633 0.546
42111 4 2m
1'4 1
" 02
NH"H 2PO .. (ADP) KD zPO"
r oll r~1
1'41 1'4 1 1'41
= 8.6, 1'33 = 30.8 = 1'51 = 2R, r 22 = 3.4 = "61 = -r2.'2 = -"52 = 0.2 = r 2 1 = - I ' l l - 0.93 = r ·.., = 8.77 , r 6J = 10.3 = r ~-,- = 8, "fl.1 = 11 = r 5 '2 = 23.76 , 1'63 = 8.56 = r .;;,., = 23.41, 1'0:' = 7.820 = r Y2 = 8.8. I"bJ - 26.8 =
" 23
~-
(KD '~P)
43m
GaAs
3.60 .3,42
43m
.3.34 J .29
InP
.1.20
43m
43111
~.. I;()
ZnS e /3-Zn S
2 .3() .
_-
-- _. _. _
= fl o =n 0 = !'lo
0.9 1.0 10.6
= II .)
I .Of)
- .
1 . ~)5
II ('
{l ( , , , . J._~.)
=1? = II
O.h
0
- - -- - _ . _ - ~ _
..
~ . _- - - -
1'41 = Tel l
I" - , :> -
= r '-,
=
1" '.1
= 1.1
-
r 'i J
-- 1.5
r 52 = r I1.; = 1.6 - . rj : ~ = . r :. = L.-+5 lJ = 1'5 2 -.. rt> 3 - 1.3
r .j J =
"-I t 1'-11
F-l 1
r~!
= r·, '- = -, = - r J_
r() .~ =
1""\ ). )'
2.0
= 2.1
._--
_.
FLEC~(ROOf'T'C
:512
Passing axis
,\;-iD ACOUSTOUPTJC MODULATCiZ:;
x
x
>
Output
y
,,
Polaroid
Polaroid
+V(t)Figure 12.1. A longitudinal amplitude modulator in which an applied electric field is biased along the direction of optical wave propagation,
the new principal optical axes such that the index ellipsoid can be described + ~ K )ij matrix. A coordinate rotation of 45° on the x-y plane gives
by a diagonal (K
1
X=
Ii
y
- ( -X'
(x' + v')
1
Ii
+ y')
(12.1.15)
Substituting 02.1.15) into (12.1.14), we find 1
( 12.1.16)
We may rewrite the index ellipsoid as ,
,1
)
X -
Y-
,:- + n,
Ii)'
,:-
1
z~
+
( 12.1.17)
1
.-, n~
where n ,x =
1
,
1/" - - - - -
(1 --
r (;:.ll ;, F. )
,.
J ,i'
"'"
1/ o
-
0
+ - ".' Il '-, F 7
I)
~
( l:?.l.lSa)
and, similarly. ; I'
L;
--1I
'2
~ F ' " ,.
( i2.1.18b)
12.1
LLECTEOUPllC
EFf~h(·TS.<\ -I[.
AMPLITUDE MODULA lORS
513
vYe note that in the new coordinate system (x'-y'··-z), the matrices (K j.K)ij and E tj are diagonalizcd: 1/ Il~;
0
0
1/ n'}~
0
0
Eo(K + t1K)
,
0 = E=
°
lin;
Ex
0
0
0
Ey
r
0
0
0
Ez
+
(12.1.19)
,2 , ,2 d E = neEo' 2 F l ' In . where Ex, = nxE or a pane wave propagating z o, E y = nyEo an the + z direction and polarized in the X' direction in a crystal described by diagonal permittivity tensor (12.1.19),
E -- x"'E 0 e i /3 z
( 12.1.20)
It is easy to show (Problem 12.2) from Maxwell's equations that the propagation constant f3 is
(12.1.21 )
where k: larly, for
=
(Ih! /-LuEu
=
27T /
"'0
and
"'0
is the wavelength in free space. Simi-
E -- y"'£ 0 e i /3 z
(12.1.22)
we find the propagation constant is f3 = kn'y. The incident optical field, after passing through the polarizer, can be expressed as E
st: 1I e i k z
=
"I
= X
Eoe ikz + y --e Eo ik~"I
(12.1.23)
12
fi
in free space. Upon hitting the surface at z = 0, the wave is decomposed into two orthonormal polarizations along the x' and y' directions; each satisfies all of the Maxwell's equations independently since both are characteristic polarizations of the crystal. The propagation constants of the .e and Y' components are kn':.' and k,(., respectively. Neglecting the reflections at the surfacex z = 0 arid .2 = the optical field at z = t can he written as
e,
.
E
r :
..... 1:' I ~ 1.:,' "-' ,.. ' ...:...
£J
.l
-
/ j
V.:..,
..' p
v
II, n
"I.
I
,.., I
.L I
"
>
..
.:.
0
__
. . ' .: pI/.:. II ,. I
/:- v
7 -
.
(12.1.24 )
ELEc r RO C) PTIC o'\ L D AC( iU$ r O :) PTIC
514
MODUJ.ATOR~;
Th e transmitted field passing through the se con d pol aroid is th e y cornponentofEin02 .1.24), or y . E, using Jy: J = Ct - Ji) /12 and yJ = ( x + y)/{i:
(12.J.25) The transmitted power intensity divided by the incident power intensity proportional to
1S
(12.1.26) Noting th at F/t) t = vet) is the applied voltage , we defin e ~-r ' the voltag e yielding a ph ase difference of 7T between the two characteristic polarizations, that is, k(n~t - n'y) t = Ti",
(12.1.27) and obta in
( 12.1.28) By vary ing VCr ) = Fz(t) t , the o u t p u t light intensity is modulated. To obtain a linear respons e, V ( l) has to be biased near V-rr /2 wh ere th e transmission factor is 50 % , as s ho w n in F ig. 12.2, i.e .
V( t)
( 12 .1 .29)
and the transmission factor is PI = Sin 2 ( JI Pi 4
I[
+
O 1TV sin w 2V;;m
l-'_o
- :- 1 + sin ( 7 V sin w ) -
V't t
t)
'"
t
] ]
( 11.1.30)
12.\
ELECTROUPTIC
E~FECTS
. 'J P,fP i = sin-
At'i;) A:v!; t.i
~
I I -1_!. I
,ViODUIATORS
5i5
(reV2V~ (t",) I
0.5
n n.r:
-
- - - - - - _. 0.5
_
I
Figure 12.2. Transmission of a light intensity in a longitudinal amplitude electrooptical modulator. The applied voltage V(t) is biased at a de value Vr r / 2 .
We see that for a small input signal zr Va « V7T , and a bias at the 50% point, V7 T / 2 , a linear response can be achieved. However, since Vr, is typically very large, a better way is to add a quarter-wave plate between the electrooptic crystal and the output polaroid, with the two principal axes of the plate along the x' and y' directions such that an extra phase difference of 1T /2 is introduced between the x' and y' components of 02.1.24):
Eo E = V 2 ( _t' e .17T/')- e Isk• n'n r f
+ y' e 'k ' f) I
II,
(12.1.31)
(12.1.32) .f
In this case, the modulat ion voltage is VU) = Va sin No de bias is necessary.
12.1.3
(IJ'/I
t instead of 02.1.29).
Transverse Amplitude Modulator
A transverse amplitude modulator is shown in Fig. 12.3 in which the applied field is biased in a direction perpendicular to the propagation direction of light. The incident optical electric held nfter passing through the polaroid is
E.I
EL FCTROOPTIC A N D ,-\COUST O \"',P f JC MJDULXi"ORS
5 16
AzF z
,z
z
z
z
- - - --
,
y' ",
,,
~x'
,,
,, y' =
Polaroid
t
Polaroid
Figure 12.3. A transverse ampl itude modulator. The bias field iFz is perp endicul ar to th e dire cti on of opt ical wave pr opagation .
propagating in fre e space. Note that the direction of prop agati on ha s been ch os en to be along the y ' di rection of the electrooptic crys tal, which makes an angle 45° with the principal x and y axes of the unbi ased crys tal. After passing through th e crysta l, the x' and z components g ain different p hase s at y' = t:
(1 2.1.34) Here, we still use KDP crystal in our analysis. The tran smitted field throu gh '- he secon d polaroid with the passing axis given by ( - ,i' + Z)/fi is
E = E . (
2
- xA, + z~ ) (
f)
v-
E0
= - ? ( - e ' k fI , r + el k < t ) "I
"
fI
-
Th erefor e, we finel th e transmission factor .'
(1 2.1.36 ) where
(12.1. 37) Here th e time-d ependent Iie lcl f~{t) m o dLll ~lte s th e pha se (p( t) , whi ch deter-
12.2
PHASE MODUwl\.TOR "
5L7
mines the output light intensity a s () function of time. Since F/O = V(t) /d, where d is the thickness of the crystal , we nne! that the phase difference between th e two characte ristic polarizations (£ ' and components) is, from 02.1.37),
z
Vet) d f
(12.1.38)
Again we can define a half-wave voltage V1T as the voltage required to introduce an extra phase shift to 77":
v
=
1T
277"
kn ~"63
(d)
( 12.1.39)
t
vVe can see that the factor d / t can be cho se n to be small; therefore, the half-wave voltage V, is reduced compared with that for a longitudin al amplitude modulator. We write
¢
=
k t' 77" V e t ) - 2 (n o -n ,J + 2 V1T
( 12 .1.40)
The transmission factor is then
(12.1.41) A linear response is obtainable if we choose
kt
71
----;-(11 1) - Il e )
4
( 12:'1.42)
and the input sign a l V( t ) = v~ ) sin (,)"" is small , Vo « V1T , The transmission factor is rhe sa me as (12 .1.32) and is similar to Fig . 12.2.
12.2
12.2.1
Pl:-L-\SE IVIODULATORS
Optical Phase M udula tion
Consider an in cid ent opt ical {k id pr op a guti n g alon g th e z dire ction and passing thro ugh th e pol a r. .lcl a~; s ho« n in Fig. 12.4: l~'
1...,
__ "': / r~ . \ 1:..
c:
-,
L:
11-. :."
') t ) l' 17~._.
ELL~CTI~OUPTIC I\N
SIS
0 ACOUSTOOPTiC MODULATORS
Passing Axis r x -v
Polaroid V(t) Figure 12.4. A longitudinal phase modulator with an applied electric field iF~(t) along the propagation direction of optical field E.
Since the polaroid has been aligned such that the passing axis is along one of the characteristic polarizations of the electrooptic crystal, x', the transmitted field at z = f is simply E I = X"'E oe ikn't .r
(12.2.2)
= x'Eo eikll"t eikn>uJF:(I)f/2
(12.2.3)
Therefore, if we modulate the applied electric field as (12.2.4)
we find (12.2.5)
where r r r'I F. k -263 0 0
l
iJ
(12.2.6)
The electric field in the time domain is
E,(f,L) = Re(E,e-I'AlI) =FEf)cl)s(kn(}t+ osinlrJl/IL -
Wl)
(12.2.7)
The phase of the output optical field is modulated by the factor 8 sin we use the mathernurical identity [10] --;-... ~
t
j'~})
"nt'
C.
(--: i '11 ( '!.J + 7i,l 2. }
wml.
If
. ., "J' (. 1)_ ...c..0
-
_..
_._~
.~~--
-- - -
12.2
PHASE MO j) "l JLA TO i ' S
:5I Y
or, equivalently, .:,t:,
e j,)
si n
"W
} ( 8) e im lD
(J 2 .2 .9)
/II
1/1 ..~ -
' ,I)
Equation (12.2.7) can als o be written as
Et( t,t)
Re(Ete- i
=
=
~ Re [ x'Eo e i(k,, _
Re(i'Eoei(kll ,J - w( )e ioSinw",t)
~~
( -w ,j m
cc
f m ( b) e im w m' ]
xAlE 0
=
( 12.2.10)
'11 =
-
0'0
The output optical field contains, in addition to the fundamental frequency (() with an amplitude 1 oUj )E o, various sideband s with frequencies, co +, (() m ' W + 2(v m , . . . , etc. , with corre sponding amplitudes +1 1( 0 ) £ 0' 1 2( 0 ) E o, ' " . Note that 1 _m(o ) = ( - l) 1m ( 0 ). If the m agnitude 0 = 2.4048, the root of the zeroth-order Be ssel function (1 0 (0) = 0), all of the power in the fundamental frequency w is transferred to the nonze ro-ord er harmonics. Jn
Example LiNb0 3 has a 3m point-group symmetry and from Table 12.1 its 'n matrix has the form [1, 11]
r=
-
0 0 0 0
-'22
'13
'2 2
}"13
0
'3 3
' 51
0
r 51
0 0
1" 22
where
r 12 r 42
= - '22 = I" SI
' 23 =
'u
r; l -
- r 22
0 0
Th e r va lu es a t a wavele ng th Ao = 0.633 /-Lm are r u = 8 .6 X 10 -- 12 rn y V r 'n
= 3 .4 X 10-
l2
my V
1'33
=
30 .8
X 10 -
12
m ,' V
r5 1
=
28.0
X
10 -
12
rn y' V
T he r efractive indices of LiNbO J h ave a un iaxial form: II, .X ~o, ,"Z
,I '
= .II
{I
:;.; '). . . ._ ') ~. / 1 7
"'1 ,' 1, '
,
i
,'
-t
::.
_. -
1/•
e'
-
'-
'") ')O {~ ,~ . ,,,", u
(12.2.11 )
ELECTR OOP'rlC AND ACOVST001'lI C MonLJLAT()R ~
described by C' 0
L (K
+ 0. K ij )
ij
1
XI Xj
i ,i
or using the sy rn rnctry in the
X 2( ~ no
- r 22F 2
r m atrix,
+ r 13F J ) + y 2(~ + no
F 2 + r l3 F 3 J
rn
+ z' (~; + r 33F3 ) + 2yzr S jF 2 + 2 zx r 5l F, - 2xyr"F j
~
1 (12.2.12)
Since " 33 is the large st coefficient , a n applied e le c t ric field alo ng the z d irection will be most e fficie n t for the e lectroopt ic c ontrol. T h e re fo re , for F, = F 2 = 0, the index ellipsoid is given by
or
x2 n 7x-
y ?-
+
1
..,
Il;
(1 2.2 .14a )
w he re the new refractive indice s a re n ,,' -- n,y --
11 0 -
3 .!..2no rUF 3
( 12.2.14b) ( 12 .2.14c)
12.2.2
X-cut LiNbO 3 Crystal
For an Xvcut LiNb0 3 crystal , as s ho w n in Fig. 12.5 a , two elect rod e s are placed symmetrically on both s ides of th e wave g u id es such th at th e bi a s fiel F = i F) is a lo ng the z dir ection a nd th e index ellipsoid is d e scribed by 02. 2.14). An incident optical electric fie ld with TE polarization will transmit as
E -- -;E ()
eikll c Y
-
-
(,, = { )
..!:E
,,, :/,".. /-i(1/2)/lJ' r llF 1 t'
( ) '-
"
,
(1 2 .2 .15<1)
S imil arl y. fo r T M p ol ari z at ion ,
( 12.2 . 15b)
J2..~
PHI\5lE fv'IUDULJ.T01'.S
51\ ~x
(a) X-cut LiNbO 3 phase modulator
z'~
.
,.y
~7~7%. /(ql
I' -----:c:==:;::--.---~-=~ I : '- _~ __ - 'r.,y L~ rf7'..' - -_ _-~ 1
~=JJA
TM
T~>
'------..=.:{-.:----~_ .
F '"' ZF z
. )r.V77~ffiWffi/~
--f"\JL->
"".v~
Incident
Transmitted
light
Electrooptic substrate
light
y
z
(b) Z-cut LiNbO, phase modulator _ __ z
------===__-....
..,\c-----:l2z(ZZ21
~~~~~
I '• I. _ -
t>~v
- -_-(___ ~ V_ ~-
VI
I
~
------~---~-
"-~~~~~~~~~~6::::6:~-'~'" Transmitted light
Incident
Light
Electrooptic substrate
Figure 12.5. Electroopric phase modulator using (a) X-cut LiNb0 3 substrate. where th e electrodes ar e pl aced symmetrically on both sides of the waveguide, such that the bias field is along the z dire ction; and (b) Z-cut LiNbO 3 substrate, where one electrode i::; placed dire ctly above the wavegu ide: such that the bias field in the waveguide is along the positive (or negative) z directi on tor the most efficient phase modulator since fJ3 is the largest electrooptic co e fficie n t.
Therefore , 'IE polarization should be used for most efficient ph ase modulati on since r J 3 > r 13 . 12.2.3
Z-cut LiNbO J Crystal
For a Z-cul LiNbO 3 crystal as shown in Fig. J2.5b, the electrodes are placed such that the wav e g u id e is below one of the two electrodes where the field is perpendicular to the Z-cut surface and :F = iFJ . The optical transmission field will he (TE polarization)
( L2.2.16a)
{ T IVl polar iz ati on)
( 1.2.2.J6b)
LI n d
E=
In thi s c a se . TM p ul~lriz;Jtiull i..., preferred Ior n :'j)S[ effici ent phase m odulat[ \.)I1 . For m or e d isc uss io ns on th-.::· 'polarizut ::))1 ..uul e lec tro d e de sign s, inc] ud ing the TE a nd TM polarizario n conversions. sec Refs . 11 - ·1 6.
ELF CTROOPTIC AND I-\COUST G n l' T IC IvlODULATCIRS
521
12.3
ELECT1l00P'flC EFFECTS iN \YAVEGUIDE DEVICES
In Chapter 8, we discussed optical directional couplers using parallel waveguides. Here we d iscuss briefly the applications of electrooptic effects in waveguide structures . We h ave discussed the use of KDP and LiNb0 3 in electrooptic amplitude and phase modulators. Some of these materials, such as LiNb0 3 , as electrooptic crystals have been used in many commercial devices. Here, we discuss the use of GaAs in electrooptic waveguide devices. For integrated optoelectronics, semiconductor materials, especially III- V compounds, are 'at tractive be cause many active and passive components, such as semiconductor lasers, photodetectors, and field effect transistors, are made of these compound semiconductors. However, considerable research work is still necessary for integrating passive and active devices with desired operation characteristics. Example GaAs at 10.6 ,urn wavelength no = 3.34, r.l1 = r5 2 = JO - L2 m / V. All other r components ar~_zero.
0 0 0 r=
0 0 0 0
0 0
r-') :J_
0
0
r 63
r-l l
0 0
yF2 + iF..",
For a biased field F = iF L +
"63 =
1.6 X
0
0 (12 .3.1)
the new index ellipsoid is
1 (12.3.2) If we choose F I = F 2 = 0, F ~
-,
-,
y-?
xn~
iF." , we then have
=
z-
+ n - + 2r nJF 3 x y + o ~
~
n-o
1
(12.3.3 )
This is simil ar to that of the KDP materials, except th a t the crystal in the absence of fidei is Isotropic. or n = 11(/ Again a rotation of 45° in the .r-y plane gives .r = (x' + yJ) /{2, Y = (-x' + }.I)/v2, L'
X
-:-
,
iI ~
-
-
- -
- -_
-
_
_~
..
.r "-
I'
,
- /2
, -r
- ~ -~ , "
-" - -- - - --
( .1 2 .3
, "/1 -
II ~I'
I.
-'
(J
_ ._-- -- ~
..
_~ - -
.
<1'} , L )
12.3
~::L E CTi< ()() P
' 1.=.' L P
;1. CT S IL V.: \ :E C, UIDE:
D (~·: \, l(T S
52.3
where (l2.3.4b) (12.3.4c)
The previous analysis for longitudinal amplitude modulators for LiNb0 3 applicable to GaAs materials. D
IS
In the following examples, we consider (a) a Mach-Zehnder interferometric waveguide modulator, (b) a directional coupler modulator, and (c) a A,B-phase-reversal directional coupler, as shown in Fig. 12.6. The input (a) A Mach-Zehnder i nte rfe rometric waveguide modulator
Electroopti c Crystal
(b) A directional coupler m odulator
(c) A 6~-phase-reversal directional coupler
"\.l-Figure 12.6.
._
--J
Wu ve gu ide e l c ct roop tic d e vi c es \" ith ,·kc[l"i)l! c de sig ns. (a) A tvLl ch - Z chmk r
iute rfer umctr ic m od ulator. (h) a c! i r ec LlL1IU I cou ple t rnl !d ulatoi', an(i (c) a .:.'l./3 ·pl u s-:-revt,;r.-; al
directi on a l co up ler .
L LECTR OO PT 1C A N :) A',':. -OUSTOOPTI C
M Oi.JULATOR ~; , ,
power Pin is ta ken as 1 in ea ch case. The electrodes a re d e signed s uch th at th e a p p lie d e le c tric field is al o ng the z di rect ion . F = ±zF.. . , a nd the b ias fields in two waveguid es nrc opposit e in sig ns . Therefore , th e difference betwe en the two propag ation factors is approximately
D. f3
= k [n o + 2.1n ~ r 63 F 3 ·)
-
k (no -
1 ) 2n~r F 63
3
= kn ~r6]F3 V ( t)
= kn 3r - do 63
(12.3.5)
where an e ffective width d is d efined for th e e lec t ric field (F 3 ::= V/ d) . The import ant point is that b.{3 a V( t ). We will stu d y the transm ission charact erist ics of th ese d evices as a function of the detunin g factor D.f3 t . 12.3.1
Mach-Zehnder Interferometric Waveguide Modulator
As shown in Fig. 12,6a, a sing le waveguide is branched into two arms for a distance t and combined aga in into one arm a s the outpu t waveguide. The wa vegu ide dimensi on can be chosen to g u id e th e fund ament al mode only.
=>
Constructi ve
......--l-----,r'-------
ou tput
De stru cti ve output
Fj gur~
12 .7. An illtlSl l" 'l ( ~'.l'~ l d tiie Y -j u nc tj '-'!1 Cl l!" !', hcil- Z eh nJ c i i ntrrfe roru. .t nc W ~\\!\:: ~~,ll i,le modu l.u,».
il" L1cl i vl;'
;\:1:1
l! o;:::;lr ll d iv .:
llU tp l: b
in
<1
525 1
0...
15
h
(l.)
2>
0
c,
0.5
........ ::;l
0.. ........ ::;l
0
0
-2
- 1
0
1
~~t In
2
Figure 12.8. The output power from a Mach-Zehnder interferometric waveguide modulator as a function of the mismatch factor t1{3L.
With a proper choice of the polarization of the incident wave and the electrode design, the tr ausmitted intensity is
(12.3.6)
where the output intensity is normalized such that the peak transrrnssion factor is 1 for perfect power transmission. One way to understand this tr an ission behavior is that if the guided modes are in phase at the exit of the I junction (Fig. 12.7), they add up constructively and transmit with the maximum power. If they are out of phase by 180°, they will cancel each other. Anther way to look at this is that if they add up to a first-order mode, it will leak out over a very short distance, since the waveguide is designed to guide the fundamental mode only, resulting in a destructive output. A plot of the outpu t power POllt vs. the mismatch 1:1 {3 L is shown in Fig. 12.8. The interferometric behavior is clearly seen. 12.3.2
Directional Coupler Modulator
For an incident optical beam into waveguide a modulator, the output power is
In
a directional coupler
(12.3.7<1)
'"' \ ( 1.:.'.. .J./tJi ~
lfi
~.
I:::LECTRO DPTIC ;.\ N D I .,CO UST O O PT IC MODUL,,\ TCiRS
5 26
....
,, --,'~ I
p., '"
...... ll,)
~ 0
p.,
0.5
Kf=n
.....
::J
0.. ..... ::J
0
P ~4
·3
-2
-1
0
K £=nI2 Kf=3n12 2 3
4
b. [3 f. In Figure 12.9. The output power from waveguide a as a functi on of f:j.f3L for K f = 3 tr / 2 for a direction al coupler modulator.
7T
/ 2,
7T ,
and
and (12.3.8 )
where the input power is assumed to be 1. Since 6.f3 = f3a - f3 b = kn>63F3 = kn>63V/ d, we plot the output power Pa vs. 6.f3 t . Suppose we design the modulator with a length t such that Pa = 0, and P b = 1, at 6.f3 = 0, i.e., K t = 7T / 2. To switch to Pa = 1, and Po = 0, we require at least 6.f3 t = 13 7T, assuming the field-induced change in the refractive index affects the coupling coefficient negligibly. (Otherwise, we can calculate the field-dependent K and still use th e expressions for Pa and P b in 02.3.7) an d (12.3.8) to find the output : -we rs .) To switch from a cross state to a parall el state , the applied volta ge Las to be large enough such that 6.f3 t = 13 1T is sa tisfi ed . A plot of P, vs. 6.f3 t fo r K t = 7T /2 is shown as the thick so lid curve in Fi g. 12.9. We also plot P; vs. 6.f3 t for K t = 7T, and K t = 37T /2. W e see that complete switching from th e @ state to the 0) state is possible (fo r K t = 7T /2 or 37T / 2). For K t = 'TT , where we start with the B state at 6.{3 t = 0, it is impossibl e to swit ch to the Q9 state simply by ch an ging 6.f3 t a lo ne . This f act ca n also be checked 'wit h the switching diagram in F ig. 8.19. 12.3.3
6.~-Phase-Reversal
Directional Coupler £11-17]
The 6.f3-ph ase-reversal direction al coupler is s ho wn in Fig. 12.6c, and its ana lysis can be found in Section 8.6. The switching diagram is shown in Fig. 8.21. Suppose we sta rt with the parallel state at K t = 7T , 6 t = 0, where U = ( f3a - {31) /2. The output power is .
.' d; t
._
C;)S 2
(~' ) I.
2
( 12. 3. 9)
1
"
0.5 L
o
-4
-3
-2
-1
0
L1~e Figure 12.10. fl.{3 t for K t
=
1
2
3
4
In
The output power Pa of a fl.{3-phase-reversal directional coupler as a function of TT/2 and 'TT,
VVe plot P a vs. D.f3 t as the solid curve in Fig. 12.10 for K K t = 7T /2 (dashed curve) for comparison.
t
= 7T
and also for
12.4 SCATTERING OF LIGHT BY SOUND: RMIAN-NATH AND BRAGG DIFFRACTIONS The refractive index of a medium can be caused by a mechanical strain produced by an acoustic wave; this is called the acoustooptic effect. A sound wave creates a sinusoidal perturbation of the density, or strain or pressure of the m.iterial. The induced change in refractive index can be described as (12.4.1)
with W s = the angular frequency, k , = the wave vector, k , = 2711 As' As wavelength, and V s = W s I k: s is the velocity of sound in the medium. 12.4.1
=
Raman-Nath Diffraction [9]
Here the length of the interaction between the light and the acousti<: wave is small:
kn
t
(12.4.2)
where k: = 2T1 IA Il , n = the refractive index. of the medium, and /\0 = the optical wavelength in free space. This is called the Raman-iNath regime of diffraction (Fig. 12.11), In this case, the thin region in which the acoustic wave propagates acts like :.1 phase grating. and the diffracted lights can go to Q1 a ny different directions determined by the generalized Snell's law for a
ELECTROOPTIC AND /\COLS
b£J
I.
kn
;+-2
+1
2rrlA,
+1 0 8_1 x-direction
>-
'\
t n
n+~n
x=o
+-e~
MODULATor.,)
... k,..
~2AA
Incident
Light
~()CJPTIC
kx
-1
-2
kn Radius = k n
n
x=/!
Thin Rarnari-cNa th diffraction. The interaction length f is very short and the thin like an optical phase grut ing with the period equal to the acoustic wavelength A,.
Figure l2.ll. region
8C1S
grating:
m
=
an integer
(12.4.3) A simple analysis of the diffraction efficiency for this case E = yE/x, z, t) at x = t
IS
to consider
where
(12.4.5) has been used. We then write the field at x = t identity [IO] c'" cu:::,
J)
L n:=
using the mathematical
i "'.1,,/ ( II) e i msb
(12.4.6)
-x
and set (12.4.7)
(12.4.8)
.')29
The eJectric field at x ;' (x 1~y
-
~ t)
11, L , -C
=
t
=
then becomes
E'oei(klll'-UJI) -
;-, L.rn
»«
l'IrIJlll(~" A/'lt) U.
AO
-00
e- i ll1( k ,, ::
- w , t)
,
e illl k ,z e --i(r.v +mw,)1 (12.4.9)
Since for x > t, the electric field has to satisfy the wave equation in the medium described by the refractive index n, we should have the solution of the form 00
E
eik,w/x·-t)+ik""z-iw",1 fll
/71
= -
( 12.4.10)
00
where k zm ( V III
k.K.J?1
-
(
--n c
mk s
=
):
(12.4.JJ)
and (12.4.12)
We note that
Ws
« w; therefore,
W m :::: W,
' n) ;{f;f
and
W',
k X III
=
( -c
r
,
(mk S
(12.4.13)
The diffraction angle of the m th order is therefore (12.4.14)
or sin - (' [' ~nk s] , '. kn
12.4.2
=
sin -
I ['
,
ni
~~_)' n ): s
(12.4.15)
Bragg Diffraction
Whe n the interaction length ( between the c:)tici.l] and acoustic waves is long compared with kl1/k~, vr: h..ve the i3r
:'7.-
.~"
.'1
- _.
.-
~~
EL ECTRoorT C AND ACDUSTCOP'(IC MODUi j ·.TOIZS
2kn sin
e = ks
k d = kj+k s
+----- f
e is long Figure 12.12. Bragg diffraction. When the intera ction length f is long , a particular angle of incidence with one diffracted beam satisfying the Bragg condition 2kll sin e = k , will be observed . (AO + OB= A/n for constructive interference. Therefore, 2A J sin e = A ln.)
Bragg condition : 2 k n sin () = k ,
( 12.4 .16)
where e is the angle of incidence, which is also the angle of diffraction. There is only one diffracted beam determined by the above Bragg condition (see Fig. 12.12 ). Our a na lysis of the Bragg diffr aclion is presented in Section 12-5.
12.5 COUPL i ~D-MODE ANALYSIS FOR BRAGG ACOUSTOOPTIC WAVE COUPLER [1, 2] The analysis for Bragg diffraction can be based on the coupled-mode theory. We start with the Maxwell equations: .'V
x E
\7
x
H
=
-
a at
- j.L H
a
-D
( 12. 5 . 1)
at
where the disp lac ement vector is ( 12.5.2)
and the refracti ve ind ex varia tion is n ( r , Ii
=
!l
-I- J.1I( r,
I)
(1 7_.J- ...)'~ )
' 1-;"" ': - .... ~ . • ',.'
••
53i
Here the background refractive index 11 and the. amplitude of variation Cin are independent of the position and t . Consider a TE polarized wave E = yEv and assume that both the acoustic wave and the optical wave propagate in the x-z plane (r = .:Lt + z2). This solution E = ;",E y (x, Z, t ) satisfies Gauss's law because
o
-
V'D=V'[c on 2 ( r , t ) E ] = Oy[c on 2 ( x , z , t ) E y ( x , z , t) ] =0 (12.5.4) and v . E = 9 . vE/x, z, r ) (12.5.1) and (12.5.2):
=
0 too. The wave equation
IS
derived from
(12.5.5)
( 12.5.6) We assume the incident electric field to be
(12.5.7) and the diffracted electric field to be (12.5.8) The variation of the refractive index can be put in the form 6. n ( r , t) = D. n cos ( k
!:J.n
s •
r - wst )
_ei(k,.- r--uJ.J)
2
D.../l + _o-i(k,.-r-'''-,I) .... 2
(12.5.9)
Then
(12.5.10 )
where the sCClmL1 de riv.u ive uf E/ k\::; been ignor~d. since \\'".: ,l~;::;ume that the amplitude f) 1") i:~ slowly varying compared with the e:l.p(ik/ . r) dependence and T/ is now ~11011:s the direction of :\./. A similar expression holds for \;2Ei/'
ELE CT RO OPT:( ' /-\. 1\: 0 A C O L ) ~TOOPT J C t\IOOULATOR:)
. 1,"
J _, • .
The term containin g t he product of ~11(r, t)E will give ri se to four terms:
(12.5.11 ) and a similar expressi on holds for ~!l(r, t)E d' Notin g that the total electric field E = E, + E d' we compare the terms of the same spatial and time variations and find
(12.5.12) or
(12.5.13) These results are illu strated in Fig. 1.2.13. Equation 02.5 . .12) shows th e . conservations o f momentum and energy for a photon with initial wave vector k , absorbing a phonon with a wave ve ct or k , resulting in a final photon st at e with mom entum Izk d = hk; + Ilk s and energy fIw d = h ca, + flC.lJs- Similarly, 02.5.13) corresponds to the emission of a phonon from the incident photon. Here II is the Pl a nck constant. Al so not ing that k , = ( wi/c ) n, k d = (wd /c)n, we find fr om 02.5.6) a nd 0 2.5.1 0)
aE.
ik.· 'VE. = i k -' I I art I
W ,? ! I
- - -;> .6. nE d ( r ) 2 c-
Since f; is along the direction of k. and r d is along the direction of k take r = xf , and
ri cos () = x
Ttl
cos 0 = x
=kj
+ ks
kd = k j
lOJ = 0\
+ CU s
0)d
kJ
,a)
et ,
we
(12 .5.14)
-
ks
= cui -
COs
( b)
Figure 12.1J . T he di,lgra :11:> to r th e d irtru c tio n uf lig h l nv so und : (a) k rl und (b) k " = k ; - k .\ . (U , i ;:; l V , - (!I . .
= k , + ks'
( 0"
= U)i
+
(') s
L'. 5
BRAG:"'; ACO l) ";TO ;)] 'TIC 'S.\ VE CDl:PLU,S
533
We obtain dEi dx
iK .E[
=
I
2 c cos
I
Kd
Since
W S «(U I' , Wd
we have
W d :::::: W i
K=
(12.5.15a)
e
w(f6.n =
= wand
2c cos
(12.5.15b)
e
K, :::::: K d
= K:
w6.n
2c cos
(12.5.16)
(j
The solutions for the coupled-mode equation given the initial conditions E/O) and £/0) are
E i ( x)
=
EJO)cos Kx + iEAO)sin Kx
EAx)
=
Ed(O)cos Kt + iEJO)sin K"
(12.5.17)
If initially, £iO) = 0, the field amplitudes are
E i ( x)
=
E j ( O)cos K1:
£A x)
=
iE j ( O)sin Kx
(12 .5.18)
The energy IE/U)1 is co upled to IEi X )1 and backward during the interaction as th e optical waves propagate along the x direction , as shown in Fig. 12.14 . We can write that th e diffraction efficiency at a length f! is 2
2
(12.5 .19)
TJ
.....
, ,,
>,
~
J::
-~
I
0.5
,,
,, "
/~"'-IEix)F
I
I
,, .#
0
,
I
•
~-"--"-----'-"'=:'-~--'---''----<--
rr/(2KJ
x/K
Positi on x Fi~uri~ 12.1-t The coup l i ng \ l l' l' ·; ·.', ;:;. i,;' o. betwe en t l . c i l1~'ilk! ,l ac o us toop tic me drum in w hich a SPl l ,1(1 wave P Wr'_~? ~l tl·S.
~1 11 :J cli !ri~IClccl ( 'ptI C I] \\ ~!v ,-'S ill ~In
ELEC T ROOF t'le AND f ,COUSTOOPTIC MODUlATORS
PROBLEMS
12.1
Calculate the voltage parameter V.. = ). 0 / (2 tl ~ 1'63) for the materials an d wavelengths with the nonzero 1"63 coefficients in Table 12.1.
12.2
Show from Maxwell's equations that for a permittivity tensor in the principal axis system,
o Ey
o (a) a plane wave polarized along the principal axis i and propagating along the z direction, E -- i.E 0 e if3 ;:
the propagation constant is f3 = w-{M,e x; (b) a plane wave of the form E = yEo e it3z will have a propagation constant f3 = f.L e y .
wJ
12.3
For a longitudinal amplitude modulator as shown in Fig. 12.1 , (a) if the bias voltage is V(t) = (0.5 + 0.1 s in W I1l t plot the output light intensity as a f unctio n of time. (b) Repeat r:clrt (a) if Vet) = 0.5V7T sin wJlJ .
12.4
Mod ify the design in Fig. 12.1 by adding a quarter-wave p la te such th at the transfer function 0 2.1.32) can be realized with a linear response and the bias voltage vCt) will not require a de bias voltage .
12.5
For the transverse m odulat or shown in Fig. 12.3 , plot the transmission factor PI /Pi vs. time, as suming that
12.6
A quarter-wave prate is ad ded immediately a fter the first polaroid in th e tran sverse amplitude modulator in Fig. 12.3, and the ele c troop tical m aterial is GaAs ' » , = fl o = 3.42), assuming that the wavelength ,~ () is 1.0 f.L 111. The electric field E i is circularly polarized
.'
)v:..,
'1:;'
e,
I
~-=
(
.r" I
,
r
j --
-;-:: ,~'"
I
befo re impi ng ing o n th e GaAs cr ystal.
-~) /E2o e 1'1 . \ " fl .
5::15
(a) Find the electric field E~ at y' = t' in Fig. 12.3. (b) Find the transmitted field E 1 after passing the exit polaroid. (c) Obtain the transmission factor PI/Pi and plot it vs. time for V(t) = (Vrr / 4) sin (U n / · 12.7
Consider a transverse elcctrooptic modular, as shown in Fig. 12.15. The incident electric field is randomly polarized and only half of its power passes through the polaroid. The crystal is a KDP with an ac electric field applied in the z direction, and the refractive index ellipsoid is described by 110 on the x-y plane and n e along the z axis before the ac field is applied. (a) Find the expressions for the optical electric fields Eland E z . (b) Find the expressions for the electric fields E 3 and E 4 after they have been reflected from the perfect mirror. (d Assume that the applied ac electric field across the modulator in this problem is_f/t) = F zu cos wt. Find the ratio of the output optical intensity to the incident optical intensity as a function of time. Use a graphical approach to illustrate your solution assuming that
kf -en -n 2 e
0
)
8
(d) If we have a dc applied field, F, = Eo, find the value Eo such that the .ncident light Pin is completely absorbed by the system. z z
PIN Incident liaht =::) o
---r------+---.~
x'
x'-
'-
e
Figure 12.15.
12.8
(n)
E"")
~
Reflected light
For A Ga As transverse .modulator, derive the index ellipsoid for
F
F j .1.: -+ F 2 .v
=
-I-
p.,,£
(h) If F is along th~ ( I l I) direction. i.e ..
F
( .t =.:.:
-~
0 -T·· ::) }-I)
.-.•- .------------------
"' V/ _J
•
.~
•
' •
•
••
~
'
. "
: .'
,
,
:'\'
-...~ .. :, . , . .
M •
•
•
•• • •
, ••
,: .. ,
~
...--
.
•
•
• • ~ • •• • ~ :' ~
•
ELE'::'TRCl(IPT!< ' !'.N }) ACOlSrO OPTI C MOD',JLA'(Of{S '
design a tran sverse modulator anel calculate the voltage parameter Vor . .
12.9
Discuss the design of a phase m odulato r using Gai\s compared with .th a t for LiNbO J used in th e text.
12.10
For a Ga As phase modulator, compare the longitudinal configuration in Fig. 1.2.4 vs. a possible transverse configuration such that the direction of the applied e le ctric field F is perpendicular to the direction of the optical wave propagation.
12.11
Derive 02.3.5) and (12.3.6).
12.12
(a) Check the output power Pa in Fig. 12 .9 using (12.3.8) for K
Tr / 2. (b) Plot P,
VS.
(!1f3 t / rr ) for K
t
t
=
2Tr.
=
12.13
Plot the output power PIJ VS . 6.f3 t / pler using 02.3.9) for K t = 3 tr / 2.
12.14
Derive (12.4.9)-(12.4.12).
12.15
D erive the coupl ed-mode equations in 02.5.15a) and C12.5.15b).
77" [or a
~f3-phase-reversal
cou-
REFERENCES 1. A. Yariv, Optical Electronics , 3d ed. Holt-Rinehart & Winston , New York, 1985.
2. H . A. Haus, Wan's and Fields ill Optoelectronics, Prentice -Hall, Englewood Cliffs, NJ, 1984. 3. B. E. 'P... Saleh and M. C. Teich. Fundamentals of Photonics, Wiley , New York,
199( 4. S . Ada ch i, Phy sical Prop erties of ]/J-V Semiconduct or Co m p oun ds , 'Wiley, Ne w York, 1992.
5:' K. H. Hellwege , Ed. , Landolt-Bomst ein Nltme;ical Data and Functional R elation ships ill Science and Technology , New Se ries, Group III 17a , Springer , Berlin, 1982; G roups HI -V 22a, Springer, Berlin , 1986. 6. K. Tada and N . Suzu ki . "Lin ear el ectrooptical properti es of IrtP. " Jpn . 1. Appl. Phys . 19,2295-2296 (1980): and N. Su zuk i and K. Tada, "Electro optic properties and Raman sc att erin g in InP," Ipn . J . A pp l . Phys. 23, 291-295 (1984).
7. S. Ad achi an d K. O e , .. Linear e lect ro-o p tic effe cts in z incble ride-typc se rnicon.iuctors: Key properties of inGaAsP rele va nt to device design, " 1. Appl. Ph ys, 56 , 74- 80 (19S·D; and "Qua d rnt ic e leciroo pti c (K err ) effe ct s in z inc ble nd e -typ e sem ico nd ucto rs: Key prope rt ies 1) [' InG a A.'.;P re lc vun t to device design," 1. Appl . Phys . 56 , l499-l5()4 (l 9K4).
:'> . S. Adachi , Prop erties
orln diu rn PJi m p hidc,
Engin eers. London . 1')9 1.
INSPEC, The In sti tute .o f Electrical
PErF,RENCE>;
537
9. A. K. Ghatuk
l l. S. Thaniyavarn, "Optical modulation: Elcctrooptical Devices," Chapter 4 in K Chang, Ed., Handbook ojMicrowat:e and Optical Components, Vol. 4 of Fiber and Electro-Optical Components, Wiley, New York, ~91}1. 12. H. Nishihara, M. Haruria, and T. Suhara, Optical Integrated Circuits, McGraw-Hill, 13. 14. 15. 16.
New York, 1989. T. Tamil', Ed., Guided-Ware Optoelectronics, 2d ed., Springer, Berlin, 1990. R. C. Alferness, "Guided-wave devices for optical communication," IEEE 1. Quantum Electron. QE-17, 946-959 (1981). O. G. Ramer, "Integrated optic electrooptic modulator electrode analysis," IEEE 1. Quantum Electron. QE-18, 386-392 (1982). D. Marcuse, "Optimal electrode design for integrated optics modulators," IEEE 1. Quantum Electron. QE-J.8, 393-398 (l1}82).
17. H. Kogelnik and R. V. Schmidt, "Switched directional couplers with alternating 6.(3," IEEE 1. Quantum Electron. QE-12, 396-401 (1976).
13 Electroabsorption Modulators Electrcabsorption effects near the semiconductor band edges have been an interesting research subject for many years. These include the interband photon-assisted tunneling or Franz-Keldysh effects [1-3J and the exciton absorption effects [4-9]. With the recent development of research in scmiconductor quantum-well structures, optical absorptions in quantum wells have been shown to exhibit a drastic change by an applied electric field [10-13]' Wh i1e previous excitonic electroabsorptioris in bulk semiconductors were mostly observed at low temperatures , sharp excitonic absorption spectra in quantum wells have been observed at room temperature . These so-called quantum-confined Stark effects (QCSE) [11, 12] show a significant amount of change of the absorption coefficient with an applied voltage bias because of the enhanced exciton binding energy in a quasi-two-dimensional structure using quantum wells. The quantum-well barriers confine both the electrons and holes within the wells ; therefore, the exciton binding energy is increased and the exciton is me difficult to ionize . The analytic solutions for pure two-dimensional and three-dimensional hydrogen models in Chapter 3 show that the exciton binding energy of the Is ground state is four times larger in the 20 case than in the 3D case (14]. The sharp excitonic absorption spectrum with a small scattering linewidth shows the possibility of a big change of the absorption" coefficient by an applied voltage bias. The change in the absorption coefficient can be as large as 10 4 em - I in GaAs / Al xGa I-x As quantum wells [10-13] . Interesting quantum-well electroabsorption modulators at room temperature have be en the subject of intensive research recently. In th is chapter we discuss the theory for electroabsorptions with and without excitonic effects. In Section 13.1 we present the effective mass theory for a two-particle system: an electron -hole pair. The general formulation for the optical absorption due to an electron -hole pair is discussed . We show th at a change of variables from the electron and hole position coordinates r e and to thei r differe nce coordinates r = r ", - r h and their center-of-mass coo rd ina tes R lea d to po ssib le an a lytical solutions [4, 5, 8, 9] when the interaction potentia! is due to (l ) an e le ctr ic field only, which leads to electroabsorption effe cts in whi ch a ligh t is incident , or (2) the Coulomb interaction between the electron '.lnd th e hole, which gives the excitonic
'It
5YI
absorption when a light is incident, or (3) both an electric field bias and the exciton effects. Case 0), the Franz-- Keldysh effect, is discussed in Section L3.2. The exciton effects, case (2), are presented in Section 13.3. Both have analytical solutions for direct band-gap semiconductors near thc absorption edge. Case (3) in a quantum well, presen ted in Section ] 3.4, is called the quantum-confined Stark effect. The general solutions are obtained using two methods: One is based on a numerical solution of the Schrodinger equation in the momentum space for an electron-hole pair confined in a quantum well with an applied electric field [15]. The other method is based on a variational method [11, 12], which is commonly used in the literature because of its relative simplicity and accuracy especially for the bound state energy of the Is excitons. Device applications including quantum-well electroabsorption modulators [16, 17] and self-electrooptic effect devices (SEEDs) [18-20] are discussed in Sections 13.5 and 13.6, respectively.
J3.1 GENERAL FORMULATION FOR OPTICAL ABSORPTION DUE TO AN ELECTRON-HOLE PAIR In Chapter 9, we derive the general formula for absorption coefficient in SI units:
n ( It w)
=
r
2 Co V.I
1< fie n, op"
r
e . pi i) 12
0 ( Ef -
e, -
It w ) [ f (EJ -
f ( E f) ] (13.1.1a)
')
nrcEumuw
(13.l.1b)
The absorption coefficient depends on the initial state Ii) with corresponding energy and the final state if) with corresponding energy EJo The summation over the initial and final states taking into account the Fermi occupation factor f( E) of these states gives the overall absorption spectrum. We also note that the delta function accounts for the energy conservation and the matrix element in (13.1. I a) takes into account the momentum conservation automatically, as has been discussed in Chapter 9, where no interaction between the electrons and holes is considered.
r;
Two-Particle "Va ve Function and the Effective Mass Equation
13.1.1
To describe an elccrron-f.olc pair ~t(H';, rhe two-p :.111 icl '2 \N,-lV,~ function rl., can be 1,/;( r .' T.,) for an -: lectron ~\ t p():,i non r,. '.! t1d a hole ;tt uosition . I'
I
54Q
ELEC ,'RO Af: SORPTION MODULATORS
expressed as a linear combination of the direct product of the single (uncorrelated) electron and hole Bloch fu nctions, !/Jedr) and 1/;,. _ k,,(r/), respectively:
L
LA(k e , kfJI!JCk/r ,Jt/J/' --k,,(rh)
he
hi>
(13 ,1.2)
where A(k e , k 1,) represents the amplitude function. Note that the Bloch functions ~l'"kfre) and rjl,"-k,,(r/) contain both th e slowly varying plane-wavelike envelope and fast-varying Bloch periodic functions. In the effective mass approximation for electron and hole pai rs, all enve lop e function ¢(r e , r h ) :is defined as the inverse Fourier transform of the amplitude function A(k e , k /,): ( 13.1.3)
which is the plane-wave expansion of the two-p article wave function, The Fouri er transform of the wave function 1>(re , r h ) is (13.1.4)
The m ajor difference between l/J and or 1 %,+ t) , have been dropped from the basis functions and only the plane-wave parts are kept. The envelope wave function e:p (re , r h) sa tisfies the effective mass equation
[E g + E c (
-
i \Ie)
-
Ec (
-
i 'l/J
+ V(r e , r hJ]¢(re,r h) = EcP(r e , r h) (13 .1.5)
where we have replaced k e in the dispersion relation E; =:; EJk e ) by the differenti al operator -i vI.' for the r e variables , an d k , in E( . == E ,"(k iJ ) by -- i VI; for the rlr variables. Using the parabolic model, we have Ec(k ,,) = 2 2 2 Jd E.(" (k h ) -- - IJ-?k * II k.. e ,/ 2 tn * I "/r j ? _nl;,. e an The Interaction potential V(r", , r/) may be of the form (1)
YI /il' \ e' 1") I.. --
eF . (, ...-- I: -- r 11 )"
(13 . 1.6 )
It is th e pote ntia l en ergy of ,I Jre e e lc ctron a nd ~l free hol e in the pr esence of a uniform electric field F. This will le ad to th e Franz- K c ldvsh effe ct [1- 3] for the opti cal abs o rp tion , as di ~ cli ss ed in Se c tion 13 .2. The interaction potential
can also be of the form ( 13.1.7)
It is the Coloumb interaction between an electron at
and a hole at rIJ. Here E s is the permittivity of the semiconductor. This potential leads to theexciton effect [4-9] in the optical absorption, which is discussed in Section 13.3. rc
Solution of the Two-Particle Eftective-Mass Equation
13.1.2
In general, for V(r", r,) = V(r e - r,), which depends only on the difference between the electron and hole position vectors, we may change the variables into the difference coordinate and the center-of-mass coordinate system, r arid R, respectively, as shown 111 Fig. 13.1a.
R= where M
=
m: +
m~.
(13.1.8)
!v!
The corresponding Fourier transform variables of r
(a) Real Space
Electron m~
o (b) Momentum Space
Fjgllrr 13.1.
(~l)
An illu~lLjl;(\11
the ditler'.'lh:c coortli n.it« \I/t',r~r"
+
1I1);r,,)i(II<~
Fou rie r trdil:;f."rm
",-:',:i',11"
+ l.'l); )
SP':ICl'.
(ill
rilt:
;'~'
ll».
l,k,('trDII p\~.,\I.'
r ...
[il'
~!IHI
i
',i
h..
',",TII)r
r .. the hole' position vector f:,.
('elltc~r-()~',nnsc
cl;"rdill~'k ';'O'cl"r
"~·;l
H
~~
til i h.,
and R in the mom entum space are (Fig. 13.1 b)
(13.1.9) respectively, whi ch can also be checked using
expj ik : r + iK . R) = expf ik , . r ', + ik , . r,J We can 'also express the above relation s as [II
= R
m "e
-
-r
( 13 .1.10)
K - k
(13.1.11)
M
and k
m *e --K
0-=
+
M
f
nz*
k
k
=
Iz
_h
lYI
From the corresponding differential operators k e =-iVe
k" = -i Vir K = - i
vR
fz 2k h2
h 2K 2
fz 2 k 2
')_nz"*
2lv!
k = -ivr
(13.1.12)
we ob tain tz 2k 2
-
-
c
-j-'
2m':
+
( 13 .1 .13 )
2m r
and
t1 2_
\-,2
2m ~:
c
_ _
-
tz l
--v 2m ~
2
Ir
tz 2 = - -- V2 2M R
-
-
tz 2
Zm ,
V2 r
Here m , is th e reduced effective ma ss, d efined by 11m ,. = (l Im : ) Th erefore , th e effe ctive mass equat ion 0 3. 1.5) becomes
[
-
tz ]. V 2
21\-1
II.
-
~ v} + V ( r) 2m,.
( 13 .1.14)
+
(l lm ~n.
- (E - E )] cP ( R, r) = 0 ( 13 .1.15 ) g
Tile solution to th e above equation GIn the n be obtained using th e met hod of the s ep a r a tio n o f variab les. noting t ha t the R de pe n de nce ' is a s im p le free particle wave fun ctio n. e t..tx- : A'.'' ;:t.h i\
l~
J. to.
~
.. ')
1.
- J(; - (~ \ r )
( 13 .1. 16)
[
~~-'1 Zrn;
-
2
+ VCr) -- &'.-'\dJ(") '
= 0.:
o
(13.1.17)
and the energy [f: is
'l" (-:;"' =
L"
1..~
l~
~g
-
(1'3.1.18)
----
Define the Fourier transform pair as ik'r
¢(r) -- "L. a( k) -e. . = -
a(k)
=
(13.1 .19a)
,(V
k
e
- ik - r
f d r¢(r) -;rr;3
( 13 .1.19b)
'rYe find
(13.1.20)
13.1.3
Optical Matrix Element of the Two-Particle Transition Picture
The optical matrix clement between the ground state (all electrons are in the valence band) and the final state (the electron-hole pair state) is described by [4, S, 13]
e . pli ) L LA *(k~"
k,,) (c,
\' \., A
k' "
(fle i k I1 P' r
-
1' 1 ,
L. L.J k
1
(, l\. <:.
keleik"p 'r
e . I
/ ;.!
) (k ) ct:
' "
e . pIL',-
11:;)
c
0" ,.+1.. " ,1;,."
1; [,
- LA ':' ( k . -- k )
r: . p " , I, 1-: )
(13.1.21)
l...
w he r..: th e lon z ..vavc lcnath (ot' dipol e ') ap oroxi.n ation t •
'-
,~
~
•
•..
.l
\.)~
1
C:-C
0 h as been used .
EU=CTF~Oi\l,SOR P·;'ION
MOD UU\ TORS
Therefore, the k selection rule ke
+
k, = k
op
has been adopted. Comparing (13.1.20) with the definition k;, = 0, we find that the matrix element is
(13.1.22)
= 0
(13.1.3), and using K = k , +
in
e . pii >:: : e . Pc£' LA ,t, ( k , -
k)
k
=
e.
PC! '
La·' (k) k
(13 .1.23) where
13.1.4
w-e' have
assumed that
e. P
CI
'
is independent of k.
Absorption Formula
The absorption coefficient is given by substituting the matrix element 03.1.23) into (13.1.1)
(13.1.24 ) n
where n corresponds to the discrete and continuum states of $(r) satisfying the effective mass equation in the difference coordinate system, 03.1.17). The equation for a Coulomb potential is the Schrodiriger equation for a hydrogen atom, and its solutions for both bound and continuum states have been presented in Chapter 3.
13.1.5 States
Physical Interpretation of 2 I
2
and Relation to Density of
Consider the case of a free electron and a free hole without Coulomb interaction, that is, VCr) = 0 in (U. 1.17). 'With K = 0, we have g' = E- E;;. Therefore, we u::;(; a new energy E measured from the band gap E<; for convenience:
(13.J .25)
54.;
In the discrete picture, we have the wave function and the energy spectrum
(13.1.26) where n == (n.t' ny, 11), k; normalization rule
=
11\.27T/L, k ;
=
n~,27T/L,
k;
= n z 2 71/
if n = n' if n -=I=- n' have been used. We check
qynCO)
=
( 13.1.27)
l/N and
1 =
L and the
-2
3/2
2
mr1 -2
27T ( fz
11vE
=
p:,D( E) (13.1.28)
which is the thr ee-dime.. .onal reduced density of states, where LI/ = [V/27T)"]!d 3k in the discrete picture has been used. (See Problem 13.1 for an alternative approach.)
.-
13.1.6 Optical Absorption Spectrum for Interband Free Electron-Hole Transitions
The optical absorption is given by integrating 03.1.24) (13.1.29a)
where (l3.1.29b)
which gives the absorption cocthcic nt clue [(,
d
free electron and hole. The
ELECTROA R ,ORPTION MODULATORS
546
momentum-matrix element of a bulk semiconductor is " I e'" . P c ( 1"-
mo
6
= M;;/ =
E'' p
(13.1.30)
where the e ne rgy parameter E p (in electron volt) for the matrix element tabulated in Table K.2 in Appendix K.
13.2
1S
FRANZ-KELDYSH EFFECT [1-3, 21-26]
Let us consider the case of a uniform applied elect ric field, VCr) = eF . r. The Schrodinger equation for the wave function cP(r) in the difference coordinate system (13.1.17) (with K = Q) is 2
1
- 11 V'2 + eF· r cP(r) = Ecj>(r) __ ( 2m,. . Assume that the applied field is in the z direction, F solution can be written as
=
iF (Fig -, 13.2a). The
( 13.2.2) where the z-dependent wave function ¢ (z) sa tisfies
( 13.2 .3) a nd the total energy E is related to E; for the z-dependent wave function
1z2 2 :. E = -2m- ,. ( k .\ + k~) + E , J
13.2.1
(13 .2.4 )
-
Solution of the: Schrodinger Equation for
3
Uniform Electric Field
The solution of the Schrodiriger equ ation 0 3.2 .3) with a uniform field can be obtained by a ch ange of va ria ble:
~
('2f7l r eF \ i: 3(! I 7' tz 2 ) ,-
2 = 1 \
-
E=)
-
eF
( 13.2.5)
lJ .?
FRAN Z · KfJ .D YSJ-)
EFF r~ C:T
Therefore ,
(13.2 .6) The Airy functions [27] Ai(Z) or Bi(Z) are the solutions. Since the wave function has to decay as z approaches + co (because of the potential + eFz), the Airy function Ai(Z) has to be chosen. The energy sp ectr um is continuous since the potential is not bounded as z ~ - 00. Therefore , the (real) wave function satisfying the normalization condition
f oo dZcPE)z)cPEzz( z) -
=
8(E z 1
Ez. 2 )
-
(13.2 .7)
00
for a continuum spectrum is
(13 .2.8) To prove that cI>£.C z ) satisfies the normalization condition, we use the integral repr esentation [27] of the Airy function :
(13.2.9) Therefore,
f O': Ai(t
.'
- a[)Ai(t - a:J dr
-x
(13.?10) where the identity
I
cl !
7.
.. .
f .
t' i f ';. i . : ) ! .o=.
:2
tt ;:; (
I\.
-7-
l:'
I
i.~L ECT '~ OA BS O P.PT i ON
MO D ULAT O RS
has b een use d. Us in g t
= ( 217l ,.. h:
eF) z 1/ 3
and
in (13.2.10), we obtain the normalization condition 03.2 .7). 13.2.2
Summation of the Density of States and Absorption Spectrum
Since the qu antum number is determin ed by (k .\., k y , EJ as described above in the wave fun ction (13 .2. 2) a nd th e co rres pon d ing energy spectr u m 03 .2.4), th e su m ove r a ll th e sta tes n for th e absorption spectrum in 03 . 1.24) has to b e repl a ce d by the s um over all th e q ua n tum numbers :
I: -I:I: f dE z n
k, k ,
wher e th e sum ove r th e energy E, is a n in tegral sin ce E ; is a co n ti n uo us spe ctr u m and a delt a func tion norm alized rul e 03.2.7) ha s be en a dop ted . Therefore ,
+
E,
+ £8 -
til" ]
( 13 .2 .12) wh ere Au is given by (13.1.29b ). Since ")
~
L
A «, «,
d 2k
=
2/ (21/ r
I")
-
m -;'J /
7T
tz-
dEl
(13 .2. 13)
w he re £ 1 = t1 2 (k.; + k; J1 2m r = tl 2 k;1 2m r i we ca rry ou t t he integration ove r £ 1 with th e de lta fun cti on a nd o b ta in the exp ression fo r the abso rp t io n coefficient:
L~:?
rR,-\N?,---KELDYSd
!~Ffl~CT
549
Let /-.) 7V) tr er :
hAF
=
(
\
-7---)
1/3
E g - hco
T=
zm ,
t.o F
( 13.2.15)
We find the absorption coefficient
( 13.2.16) where Ai'( y]) is the derivative of Ai( y]) with respect to 7J. It is interesting to show that in the limit when F -~ 0, we have
p~ [rrfilo F fAi 1( T) dT] ~
Jhw - s,
for hw > E g as expected, since a( fzw)
~ ao( F---.O
trw)
1
=
2 l?1,.
A O - - 2 ( ~-2 ) 217 Ii
3/ 2
~_ h o: - E g
(13.2.17)
Notice that the prefactor A 0 depends on the bulk momentum-matrix element Ie . PeLf = /VI;, which can be determined experimentally [24] by fitting the measured absorption spectrum' 'th the above theoretical results with F = 0 and F O. The Franz- Keldys.. absorption spectrum (13.2.16) is plotted schematically in Fig. 13.2b (solid curve) and compared with the zero-field
*
(a)
Ev
Figure 13.2. (;\) Frunz Ke ldysh effect o r phl)tu-as;~i~ill';cl abso r ptto n In d bulk semiconductor with a uniform electric l'tdd bias. (hi .'\l)~urpti'.)n spectrum ki! a n:1ii2 fIeld F,* (l (solid curve), 'Ihe dashed line is the free electron and [Kilt: ubsorpt ion spectrum ',Vii 1;C'L:i an applied electric field.
::L::T j'RU/\BSOR,'TION
550
MODl..JLATORS
spectrum (dashed curve) using (J 3.2.17). It shows the Fr anx-Keldysh oscillation phenomena in the absorption spectrum above the band gap and the exponentially decaying behavior below the band gap.
13.3
EXCITON EFFECT [4-9, 10-15]
When we consider the Coulomb interaction between the electron and the hole
VCr) -
(13.3.1)
the wave function ¢J(d satisfies the Schr6dinger equation for the hydrogen atom
[
~ V2 + Zm ,
-
v(r)]¢(r) = E¢(r)
(13 .3.2)
The solutions ¢(r) for both the three-dimensional (3D) and the two-dimensional (2D) cases have been studied in Section 3.4 and Appendix A and the results are tabulated in Table 3.1
13.3.1
3D Exciton [4, 5]
We use the most general formula (13.1.24) for the absorption coefficient:
(13.3.3a) n
(13.3.3b)
where the summation over n includes both the bound and continuum states. The' wave functions ¢n(r) have been normalized properly for both bound and continuum states as discussed in Sections 13.1, 13.2, and 3.4. 'For bound state contributions, we have the oscillator strength
, TJ
,
a ~ n'
au =
- - - , --, -
the exciton Bohr radius
J .1.:,
EXCITON EFFEC"-
55!
and the exciton binding energy
L
/I
=
Ry =
In r e 4 7
2f1-( 47/E s )
2 =
the exciton Rydberg energy
Therefore,
(13.3.4)
where E
=
hw - E g
(13.3.5)
Ry
is a normalized energy measured from the band gap E s: For the continuum-state contributions, we obtain
(13.3.6)
where the first bracket is AOp;D( E = lu» - E g ) , and the secone! bracket is called the Sommerfeld enhancement factor for the 3D case [4-9, 28]: ( 7/
I y';) e 'TT/ If'-
sinh( tr II~') 2rr1ft 1 - c-::'.T,-//i
As
E -7
C/..!,
(13.3.7)
we finel ,'I (l
--'
..::'---c;---~---~ ( ~/ E ,':11' ..
R y tt ;) ,
-+-
Tf), ( 13.3.8 )
552
t:L=.C iT.O t\[)SO RFT TON MODULATO RS
wh ich app ro ach es the 3D jo int den sity-of-stat e s rin an in terba nd tran sition wi thou t the exci to n effec ts, (fuu - E g ) / R y , p lus a consta n t 7i'. As E ----7 0,
V
( 13 .3 .9)
which gives a finit e valu e in ' contrast to th e va n is hi n g r esult of the interb and a bso rp tio n at lu» = E g • The total a bs orp tio n due to both th e bound and co n tin uu m states is given by
~ ~ [4'iT 0
') . . ,. -'-R Y a:0 _oJ
+
f:
~ 0( tau R- E
g
n =l /1
S JD
Iz W .- E (
+
y
R
S
~ 1 '1 -
1 / tl
\
y
y
If we include the fini te linew id th due to sca tte rings by repl acin g th e d elta fu nction by a Lo re ritzia n fu nction , 8(x) = (Y/ 7T )/( X2 + y2), whe re y is t he h alf-lin ewidt h normalized by R ydbe r g if x is a normalized e nergy, we find
a (tzw )
4L n=l
(13.3.11 )
13.3.2
2D Exci ton [14, 29]
.
.'
The abso rp tion spec tr um for a two-d im en sion al str uc t u re with exciton effects can also be ob ta ine d usi ng (13. 1.24):
(13.3.11)
For bo und s ta te co nt rib u tio ns . we usc
r;'
L
li
_ -
.,
(n - 2"I ) -.
( 13.3 . 13)
n ,:,
EXCITON EFfECT
553
and obtain
(13.3.14)
where e
.
(tzw - Eg)jR y again. The continuum-state contributions give
=
-
(13.3.15)
. . ..
where the two-dimensional Sommerfeld enhancement factor is
5 20 ( £ ) =
2 1+e- 2 rr/
----=
(13.3.16)
.je
The total absorption is the sum of asUzw) and ac(flw):
a( tzw)
=
1 [ + 1] + S( } (13.3.17) i)
L
A 0 2 {OC 4 3 8 e 27TR ya o n=l (n - ~)
s)
2
(n -
Notice that without the Sommerfeld enhancement factor, 5 20 ( £) is set to 1 and a /tzw) = A oj (27TR ya~). If we include the 'finite linewidth effect, we have
A a(tzw) -
-
-
0----=2 ya 27TR o
f
l
4
co
L n=l
.
1
y 3 ---------
7T(n - t) [
c
t +
+
1 1 2] 2
(n - 2)
de'
0 --;;:-
+
1' S 2D ( e')
y2
1 (13.3.18)
(£'_<)2+1'2j
ELECTVUAB~ORPTION
554
MODULATCRS
Table 13.1 Absorption Coefficients due to Exciton Bound and Continuum States 2 ./-E 1 ./- ') I m r e" e = nco - 'g AD = 7Te e' PCl' a = ~ I 7TE s R = 2 () 2 y 2 2 Ry n,CEoWln o m, \ e 2h (47Te s)
21
4)
A
Bound States
Continuum States
Two-Dimensional Exciton ZERO L1NEWlDTH
FINITE LlNEWIDTH
A0 2 'IT" R y a 02
1'" dc' 0
7T
'Y S 2 D ( c ' ) (
, _ e )2 l + '2 e
Three-Dimensional Exciton ZERO LlNEWIDTH
Ao I:=
1
11
(
~
-rra 0 n
3)_1 0(£ + ~) Ry
n
FINITE LlNEWIDTH
AD
L cc
(
n=l
2)1 3
»«:»
3
'Y/
-
rr
n, (e + 1- ) 7
n:
Ao
2
+1'
2
[X; dE' /,,1-;' S3D(e')
27T2Rya~ 0
'IT"
.
(e'-c)2+'Y 2
The above results for both 2D and 3D excitons are summarized in Table 13.1. The absorption spectra for a finite linewidth and zero linewidth are plotted in Fig. 13.3 for comparison .
13.3.3
Experimental Results for 3D and Quasi.2D Excitons
Experimentally, the linewidth y is always finite and increases with temperature. For example, in Fig. 13.4a, we show the absorption spectra [30] of a bulk (3D) GaAs at four different temperatures, T = 21, 90, 186, and 294 K. We can see that the exciton linewidth is broadened with an increasing temperature. The absorption edge has a red shi ft since the GaAs bandgap
555
13.3 EXCITON EFFECT (a) 2D(y= 0) a(fzw) 1s
(b) 2D(y
* 0),
a(fzw)
with exciton /effect
2s k - - - - - - - - - . without exciton effect ~E --4R y g
fzw
(c) 3D(y = 0)
L...-----"~-+-----_..1iw
(d) 3D(y ~ 0)
a(liw)
a(fzw)
1 with exciton s~effect
J
~
..
,,~. '>-.th
, WI
. ff out excIton elect fzw
'--~,-+-+---------,~fzw
E -R E g g
y
Figure 13.3. Absorption spectra for a two-dimensional (2D) exciton with (a) a zero linewidth and (b) a finite linewidth, and a three-dimensional (3D) exciton with (c) a zero linewidth and Cd) a finite linewidth.
decreases with increasing temperature [31]:
,
T+b
(eV)
(13.3.19)
\, \
where Eg(O) = 1.519 eV, a = 5.4~5 X 10- 4 eV/ K, and b = 204 K. For comparison, we show the exciton absorption spectra [32] of an Ino.53Ga0.47As/Ino.52AI0.4sAs' (lattice-matched to InP substrate) quantumwell structure at different temperatures in Fig. 13.4b. The quantum-well structure has a quasi-two-dimensional character since the electron and hole wave functions are confined in the z direction with a finite well width instead of being restricted to the x-y plane as in the" pure" 2D case. It is expected that the binding energy of the Is exciton in the quasi-2D structure will be between the 3D value (,= R y) and 2D value (= 4R). Furthermore, we also see the splitting of the 'heavy-hole (HH) exciton and light-hole (LH) exciton in a quasi-2D structure, while we do not observe the HH and LH exciton splittings in a bulk GaAs sample because of the degeneracy of the HH and LH bands at the zone center of the valence-band structure. The energies and absorption spectra of the HH and LH excitons are further investigated in Section 13.4. I
~·~LECTR~)'\BSORrTION
55G
i·vt{,DUJ.f'.TORS
1.2
-.
1,1
-;
E
..qu 0 .......
'-"
ts
09 0.8
l
.. 0
0.7· . 0.6
I
!
1.42
1.44
1.46
1.48
1.5
1.52
1.54
1.56
Photon energy (eV) (a)
1.8
InGaAs/lnAIAs UNDOPED
1.6
I!
::::>1.4
I .:
uJ
1\::
~ 1.2
-c rn a:
"i~'~/;~ba"""7,'~'"
1.0
~ 0.8
_ I :.
-.,.,......
. '.
m
I;
-c 0.6
I~
0.4
Ij
/'
iE : ~
:I;
.....""'..,.,-.: ...
:1
o o
0.2
0.80
0.90
1.00
c
100. 200
300
T (K)
_ _L-_-lJ
~ - ~::--~:-:---:-~_----l....
0.70
.
QJ
1.10
1.20
1.30
ENERGY (eV)
(b)
.'
Figure 13.4. (a) Band-edge absorption spectra of a bulk GaAs sample at T = 294 K (circles), 186 K (squares), 90 K (triangles), and 21 K (dots). (After Ref. 30.) (b) Absorption spectra of an Ino53Gau..n As/ Ino.52Al0.48As quantum-well sample at T = 300 K (solid curve), 100 K (dashed curve), and 12 K (dotted curve). The insert shows the half-width at half-maximum (HWHM) of I the first absorption peak as a function of temperature. Squares are measured data; curve is calculated. (After Ref. 32 © 1988 IEEE.)
The insert in Fig. 13Ab shows the measured (squares) half-width at half-maximum (HWHM) of the first heavy-hole absorption line as a function of temperature. The solid line is a fit to the expression
r '2 ( =
HWHM) =
[0
r ph
+ exp
nw L o
( kBT
(13.3.20) ) .
1
13A
QUANTUM CONFINEL1 STARK EFFECT (OCSE)
557
where f o = 2.3 me V accounts for the inhomogeneous broadenings such as scatterings by interface roughness and alloy fluctuations, and the second term represents the homogeneous broadening due to InGaAs longitudinal optical (LO) phonon scatterings with nw L O = 35 meV and r p h = 15.3 meV. 13.4
QUANTUM CONFINED STARK EFFECT (QCSE) [11-13,15]
In this section, we consider the exciton absorption in a quantum-well structure in the presence of a uniform applied electric field. The effective mass equation, similar to 03.1.5), can be written as [12] 2
(He - Hh + Eg
-
41T6 s
le
re
-
rh
I] cP(r
e,
rJJ
E(re , r h )
=
(13.4.1)
where
H= e
(13.4.2a) (13 .4.2b)
The electron potential Veere) or the hole potential Vh(r h) may also include the effect of the electric field lelF . r , or -lelF . rho The interaction between the electron and the hole is due to the Coulomb potential. Let us assume that the quantum well is grown along the z axis and the uniform electric field is also applied along the z direction, the elcstron and hole potential can be written as (Fig. 13.5) (13.4 .3a) ,
(a) F
=0
\
(b) F> 0
. Eel hI ~--~-+~--------------------
---...~""---~
Figure 13.5. Quantum-well energy subbands and wave functions (a) in the absence of an applied electric field, and (b) in the presence of an applied electric field.
:)58
ELE(:TROAl'SOR.PTION MODULATORS
and (13 .4 .3b) 13.4.1 Solution of the Electron-Hole Effective-Mass Equation With Excitonic Efl"ects
Using the transformations for the difference coordinate and the center-ofmass coordinate systems for the x and y components, (13.4.4) where M = m; + m'J:, and p = xX + procedures as in (13.1.8) to 03.1 .15)
yy,
we obtain after following similar
Since the dependence on R t comes from only the leading kinetic energy term, the solution can be written as [33] eiK,'R,
~(re' r h ) =
..fA
F(p, »..
Z/J
(13.4.6) .'
where the exciton envelope function F(p, ze'
Zh)
satisfies
(13 .4.7)
The center of mass of the electron-hole pair is thus moving freely with a kinetic energy h 2K/2j(2M). Here, identical relations to (13.1.8) to (13.1.11), for the parallel components of the real-space and momentum-space vectors exist, e.g.,
(13.4.8)
13.4
QUANTUM CONFINED
~TARK
EFFECT CQCSU
5.'19
Note that -H(
h2
ZII) =
-
d2
~- - -
2m~ dz~
+
V (z ) h
h
(13.4.9) which are simply one-dimensional Schrodinger equations for a particle-in-abox model. Let us consider
where In(ze) and gm(zh) are the free-electron and the free-hole wave functions in the absence of any interactions. With the Coulomb interaction term, the solution F(p, Ze' Zh) is more complicated. However, using the completeness properties of the solutions {In(ze)} and {gm(Zh)}, we can expand the exciton envelope function as [12, 15, 19] (13.4.11) n
m
The Fourier transform pairs for the p dependence can be written as
(13.4.12) The envelope function
ri« ze' Zh)
becomes (13.4.13)
The complete envelope function is obtained from (13.4.6), noting that all possible K( can be included:
Comparing (13.4.13) and 03.4.14) with 03.1.2) and 03.1.3), we find that the
ELFCT[.z()r\USGRPTION MODUL,\TORS
original electron-hole pair state can be written as 1,8, 9, 15, 34]
'It(re,r,J
L L
=
ketn
Gllm(kl)~Jnk)re)ljJm-kil/rlr)
(13.4.15a)
k/llnt
eik ., 'p ,.
fA
(13.4 .15b)
fn(ze)ucCre)
e:-ikllt 'PiI
IA
( 13.4.15c)
gm(zh)u u(r h)
13.4.2 Optical Matrix Element for Excitonic Transitions in a Quantum Wen The optical matrix element is obtained using Ii) = [ground state ), IW(r e , r;), and
(fie'
pli) =
LL
LQ;;~n(kt)(ljJflkJr)le . PIl/lm -kJr)
mn k e l
kilt
If > =
= L LC:m(k{)e . Pcl..Inm nm k,
(13.4.16) nm
where lnm = { ':_ oof,7(z)gm(z) dz, and PeL' = (u/r)lpluL,(r). The above matrix elemen t can be expressed al terna tively in terms of F( p, z e> Z h):
pli) =
fex-c-
dzF*(p = O,z,z)v'/ie' P ee
(13.4 .17)
oe
Noting that K{ = kef + kill = 0 from (13.4.16), we substitute the expression (13.4.11) for F(p, ze' z,,) into (13.4.7), and obtain -(E-E8
) ]
( 13.4.18) Multiplying the above equation by f,:( ze) and g,~(z It) and integrating over ze and Zh' we obtain
(13.4.19)
1:<.4
QUANTUM
«xss:
CONFINEDSTAI~KF.FFECT
' 501
where
(13.4 .20) (13.4.21) We have ignored coupling among different subbands so that only n' = nand m' = m are taken into account in (13.4.20). The wave function 4>nm(P) satisfies the normalization condition in a two-dimensional space: (13.4.22 ) This was derived using (13.4.23)
(13.4.24 ) t
\
13.4.3 i, Variational Method for Exciton Problem
.'
Two different methods are commonly used to find the solution for the exciton , equation (13.4.19). The most common approach is a variational method, which is very useful to find the bound state solution. Noting that the Is state solution of ¢(p) behaves like e -p iau or e - pI(2 a o ), the following variational form is assumed in the variational approach [12J:
<4>1 - (h 2/2m r ) \lp2 <4>14»
-
V(p) I4»
(13.4 .25)
where
4>(p)
· ( 13 .4 .26)
' ::L ~:CT 1{ \./ .\ U S O R f' T I O N MODULATOR~
<4>14> > =
which satisfies the normalization condition
1 in 03.4.22). We find
It is convenient to write in terms of the normalized parameters
ao =
(13.4.28)
and the normalized exciton binding energy
E ex
C ex
=
R
(13.4.29)
y
(13.4.30)
where the function G(x) is defined as an integral .'
\ '.
1o dt (t
te- t
00
G(x) =
2
+ X
2
1/2
(13.4.31)
)
which is a smooth monotonic function and can be approximated [55] analytically. It has th~; properties that GW) = 1 and G(oo) = O. Typically, for a quantum-well problem, Ize - zhl is finite and the argument in G(x) is over a finite range. The pure two-dimensional limit can be obtained by ignoring the z dependence and using G(O) = 1, E ~x
Thus we find the minimum at exciton binding energy.
13
=
13 2
= 2 and
-
4{3
B ex
(13.4 .32)
= .- 4 as expected for a pure 2D
13.4
QUANTUM CONF1NED STARK EFFECT (QCSE)
13.4.4
563
Momentum-Space Solution for the Exciton Problem
Alternatively, the real-space exciton differential equation (13.4.19) can also be written in terms of the momentum space integral equation [IS, 35]:
where
A direct numerical solution of the above equation is discussed in Ref. 15. 13.4.5 Optical Absorption Spectrum with Exciton Effects in Quantum Wells
The solution to the eigenvalue equation (13.4.19) is a set of exciton binding energies and corresponding eigenfunctions for Is, 2s, 3s, and continuum states. We denote the quantum number for the exciton state as x. The absorption coefficient for' a quantum-well · structure can be obtained by substituting the matrix element (fie· pli) into (13.1.1)
(13.4.35,) where the exciton transition.energy is (13.4.36a) ,
and the band edge transition energy is en E hm
--
E g + E en
-
E hrn
(13.4.36b)
The exciton binding energy Eel< is a discretized set of Is, 2s, 3s, .. ' . states and continuum-state energies. Assuming that there is no mixing between different subbands, consider only the pair n = Cl and m = HH1, for example. We
. -...-f"'"T:"t'-
'I ~ """'
__
-- -....;...,;,,--:o"""._._ ~ . ,.
• ..:_ - ."!"',- .., ._ -__
'
~
- . -.o)W>
!"".
"...c._,
~ . ~,. -
....,..".•.
~ '~. ~
_~
••'":"'
~ ~ _ ,.-:'I
I;'Y',
.. -
_. ~
••...,.-,.....-: •••-.,'
,, - ~
._
,., . _ . ~4' . ,
__
' _~ . ~
CU : ...:::T ROABSO Rf T IO r-; MODULATORS
564
m a y drop th e sum ma tio n over nm a n d tr eat e ach pai r of nand m independen tly. This ass um p tio n is va lid only if th e subba ri d e nergy differ ence is much la rge r than th e e xcito n binding e nergy . T he a bso rp tio n coeffi ci ent becomes
2 a(llw ) = C o L
L I4
-
liw)
(13 .4.37)
x
Exciton Discrete ( Lsl -S ta t e Contribution. For the Is state , we find
( 13.4.38)
.
-_..
where a finite lin ewidth 2 y h as b e en as sum ed and the delta function is replaced by a Lorentzian function and x = Is state. The matrix e le m e nt Ie' Pal is ob ta ined [15, 36] from (9.5. 20)-(9 .5.23) in Secti on 9.5 .
For TE polarization ( i = i or
y) Heavy- hole exciton Light-hol e ex citon
(13 .4.39)
For TM polarization ( i = i) Heavy- hole exc iton Light-hole exciton where
Ml
(13.4.40)
is the bulk matrix element discussed in Chapter 9: ma
- 6 Ep
( 13.4.41)
Exciton Continuum-State Contributions. For continuum-state contributions, the wave fu n ction !
2"
~ .\
a n d E ex ~
=
2" " -- A ~ ~ k, t: .v
m y;tzr2
Jd E
"{
(13.4.42)
tz 2 k {2I /(7 m r ) = E { . We obtain the absorption coefficient due to ~
......--
~
_ .. __ "'4••• • ••
~ ••
1
13.4
QUANTUM CONFINED STARK LFFECr (QCSS)
the continuum states
where Ex = E~':n + E, and l¢x(O)/2 is usually approximated by the Sommerfeld enhancement factor for a 2D exciton:
(13.4.44 ) where 1
~ So
< 2. For a pure 2D exciton,
So =
2 and
(13.4.45) The matrix-element M(E t ) is defined [15, 37, 38] as Ie . Pcvl 2 = M(E t)Mb2 , which has been derived in Section 9.5 and is tabulated in Table 9.1. TE polarization
Heavy-hole excito. Light-hole exciton
( 13.4.46)
TM polarization
Heavy-hole exciton Light-hole exciton
(13.4.47)
where cos? ()nm = (E en + \EhmD/(Een + IEhml + E). The heavy-hole exciton contribution to the TM polarization is taken to be zero instead of (~)sin2 ()nm because a rigorous valence-band mixing model shows that the heave-hole exciton has a negligible contribution to the TM case [39-43]. Note that k ; = l/a o and
----
(13.4.48)
E L E ::T K OA B ~ O R P - r I O N
56 6
MODULATORS
Total Absorption Spectrum. The complete absorption spectrum can be written as the sum of the bound-state and continuum-st ate contributions [15]:
(13.4.49) Let us look at the band-edge transition energy
E}~;~:
(1304.50) for the electron subband n and the hole subband m in the presence of an applied electric field. Note that th e subband energies are measured from the band edges at the center of the quantum well (positive for electrons and negative for holes). 13.4.6
Perturbation Method
A simple second-order perturbation th eory shows [44] that (see the example in Section 3.5 and its references)
/ 13 .4.51) in an infinite quantum-well model assum ing an effective well width of L efr . Therefore, the band-edge transition energy for the first co nd uc tion and the first heavy-hol e subba n d is determined by
( 13.4 .52) where C 1 = -2.19 X 10- 3 . As an example, for ~ GaAs/AlxGa1_xAs quantum well with an effective well width of 100 A, the above change in the transition energy is E~}(F) - E/~t(F = 0) = -U.S meY at F = 100 "kY/cm assuming that m : = O.0665mo and m~h = O.34m o' The exciton binding energy E c x also depends on the electric field strength. In general, the band-edge
13.4. QUANTUM CONFINED STARK EFFECT (QCSE)
567
a
2 1 ------l..-~C-..---___'_:7"""==----.~-.=.-------~
tu»
Figure 13.6. Exciton absorption spectrum of a Quantum-well structure in the absence of an applied electric field. The contributions due to the discrete and continuum states are shown separately as dashed lines.
shift due to the electric field is quite clear and appears stronger than the binding energy change with the electric field. Variational methods instead of the above perturbation method for the band-edge energies have also been used [44-47].
13.4.7 Exciton Absorption Spectrum and Comparison With Experimental Data
Theoretical absorption spectrum for a single pair of transitions from the first conduction subband to the first heavy-hole subband is shown in Fig. 13.6, where the discrete Is bound state Ex = E i S contributes as a Lorentzian spectrum, and the steplike density of states enhanced by the Sommerfeld factor contributes as the high-energy tail. With an applied electric field, the quantum confined Stark effects can be measured from the shift of the peak absorption coefficient as a function of the applied electric field. Figure 13.7 shows the polarization-dependent optical absorption spectra for (a) TE and (b) TM polarizations [17, 48] with estimated electric fields [13]. Theoretical results using the parabolic band model [15] presented in this section and using a valence-band mixing model [43] have been used to successfully match these experimental data, as shown in Fig. 13.8. To understand these data, we make the following observations; 1. The exciton absorption peak energy depends on the band-edge transitiop energy Ehi(F), which shifts quadratically as a function of the field, minus the amount of the Is state exciton binding energy E 15 , which is about 8 meV for the heavy hole exciton. The transition energies of the heavy-hole and light-hole exciton peaks vs. the applied electric field are shown in Fig. 13.9. The binding energy for a bulk (3D)GaAs R y is
..
'''~''--
;
/
ELECTt{ Or\ BSO RPT IO N MODULATORS
568 4 ___.----
(a) TE
2
-z 0
en en :E
en
I
0
Z
(b) TM
< a:
t-
c
~
I
2
o~~:::;;;=-.--.:::~6
1.42
1.46
~
1.5
PHOTON ENERGY (eV) Figure 13.7. Experimental absorption spectra of a GaAsjAl O.3Ga O.7 A s quantum-well wavegu ide modulator as a funct ion of field : (a ) TE polarization for (i) 0 kY/ em, (ii) 60 kY jem, (iii) 100 kYjem, (iv) 150 k Vy cm. (b) TM polarization for (i) 0 kYjem, (ii) 60 kYjem, (iii) 110 kYjcm, (iv) 150 kYj cm, and (v) 200 kYjcm. (After Ref. 48.) [13,17].
about 4.2 meV and is 4R }' = 16.8 meV for a pure 2D exciton. A quasi-two-dimensional quantum-well structure gives a binding energy corresponding to an " effective dimension" between 2D and 3D. Therefore , the binding energy of the quantum well is somewhere between 2D and 3D. As a matter of fact, since analytical solutions for the hydrogen atom equation in an a-dimensional space have analytical solutions for an integer a such as 2 and 3, the idea is to extend the general result for a given a using the concept of analytical continuation. Using this approach, the oscillator strength for the bound and continuum states can
13A
QUANTUM CONFINED STARK EFFECr (QCSE)
569
(a) TE
C
W
-< N
.J
:E
a:
o z z o
i=
a. a: o en 1'C
<
1420
1440
1460
1480
. PHOTON ENERGY (meV) Figure 13.8. Theoretically calculated absorption spectra for the quantum-well waveguide modulator in Fig. 13.7: (a) TE polarization, (b) TM polarization. (After Ref. 43.)
be obtained using the analytical formulas once the "effective dimension" is determined. The effective dimension can be extracted by comparing the binding energy calculated variationally, as discussed in this section, with the analytical formula for binding energy·[49]. 2. The TE oscillator strength for the heavy-hole exciton is approximately three times that of the light-hole exciton. However, since the light-hole exciton transition energy is already in the continuum states of the heavy-hole transition, the spectrum would not show a 3:1 ratio. 3. The TM polarization spectra show that it is the light-hole exciton transition which is dominant for this polarization as a result of the optical momentum matrix-selection rule.
}.LECTRO ;\BSDRPTION MODULATORS
5"70 1480
'-,--I-.-----r--r'
I
0
1470
:x- - --x
' - - '?+O
-x ,
--->
1460
E ..-
1450
>-
o
a:
W Z UJ
,
'>4-q
(1)
X,
,, '0
14 4 0 1430
•
HH (exp.)
0
LH (exp .)
+
HH (theory)
x
LH (theory)
1420 1410 -30
0
30
60
FIELD
90
120 150
180
(kV/cm)~_
Figure 13.9. Comparison of experiment al and theoretically calculated exciton energies vs. the electric field. (After Ref. 43 .) .
4. At a fixed optical energy tz w of the incident light, the absorption coefficient can change drastically especially when h co is near an exciton peak absorption energy. This enhanced change of the absorption by an applied voltage is discussed further in the next section.
13.5
INTERBAND ELECTROABSORPTION MODULATOR
The electroabsorption modulators can be designed [l O, 50-56] using a waveguide configuration (a) or transverse transmission (or reflection) configuration (b). Consider the modulator structures shown in Figs. 13.10a and b. Suppose the operating optical energy fzwo is chosen near the exciton peak when a voltage V is applied (Fig. 13.10c). The transmission coefficient is proportional to (13 .5.1 ) . For the waveguide modulator, a(V) is the absorption coefficient of the waveguide region multiplied by the optical confinement factor I', and L is the total length of the guide for the waveguide modulator. For the transverse transmission modulator, a(V) is the average absorption coefficient of the multiple-quantum-well region, and L is the total thickness of the MQW region. The couplings or reflections at the facets are ignored here for
13.5 INTERBAND ELECTROABSORPTION MODULATOR
(a)
571
(c) a(1ico)
a(V)
C::::=~====~tt(V) = T(V)Pin
aCO)
noo (b) Transverse transmission modulator
(d)
Vet)
~Pin
~
----,/----L..--'------'---'-----l...---+t
Vet)
-
I
~
~
Pout ~ T(V) Pin
Figure 13.10. (a) A waveguide electroabsorption modulator. (b) A transverse transmission electroabsorption modulator. (c) The absorption coefficient a.(hw) of a quantum-well modulator at two different bias voltages, V and 0, for example. (d) With a bias voltage vet) across the modulator, the transmitted optical power (solid square wave) is modulated. Dashed line is the input power Pin'
convenience. The on/off ratio (or contrast ratio) Ron/off 13.10d) Ron/off
=
Pout (Von p (V out off
= =
IS
defined as (Fig.
T(O) 0) V)- T(V)
(13.5.2a)
or in decibels Ron/off (dB)
= =
T( Von = 0) 10Iog----T( Voff = V) 4.343[ a( V) - a(O) ] L
(13.5 .2b)
Therefore, in principle, the magnitude of the extinction ratio or the on / off ratio can be made as large as possible by increasing the cavity length L. However, we note that the insertion loss Lin is defined as Lin
Pin =
Po ut ( 0) Pin
=
1 - T(O) = I -
e-o:(O)L
(13.5.3)
EJ ECTR(lAHSOEPTION MODULATORS
572
at the transmission (on) state. Since nCO) is always finite , a large cavity length L will decrease the transm issivity T(O) exponentially. We may achieve an
infinite on / oft ratio using an infinitely long cavity and obtain no light transmission even for the on -state. If T(O) -;, 0, the insertion loss approaches 100%. Naturally, this is not desirable and an optimum design, which maximizes the extinction ratio and minimizes the insertion loss, is necessary. Note that Von is set to zero here only for illustration purposes. For high-speed switching, it is usually set a nonzero reverse bias voltage for fast carrier sweep-out of the absorption region. Another useful figure of merit in the design of the electroabsorption modulator is the change in absorption coefficient per unit applied voltage. a ( VoCf )
a ( Von)
-
(13.5.4 )
~V
where the change in voltage ~ V = IVon on / off ratio per unit applied vol tage is Ron /off ----'------ =
~V
4.343
-
V:>ff I.
This occurs because the
[a(V) -a(O)]L
6V
6a = 4 .3436F
(13 .5.5)
where the electric field across the multiple-Quantum-well region is approximately given by F = V/ L, if the built-in voltage Vb i is ignored. (Otherwise 6 F = (V - Vb) / L has to be used .) For more discussions on the figure of merits, such as ~a/(~F)2, C(~V)2, and the optimization of the contrast ratio, drive voltage, bandwidth, and total insertion loss, see Ref. 56.
13.6 SELF-ELECTROOPTIC EFFECT DEVICES (SEEDs) [18-20, SO-56]
Interesting optical switch devices such as the self-electrooptic effect devices have been demonstrated using the quantum confined Stark effects. These devices show optical bistability and consist of a multiquantum-well p-i-n diode structure with different possible loads, such as a resistor (R-SEED), a constant current source, or another p-i-n multiple-Quantum-well diode (Symmetric or S-SEED). In this section, we discuss basic physical principles of an R-SEED. As shown in Fig. 13.11a, the circuit equation is given by Kirchoff's voltage law:
(13.6.1)
13.6
SELl- -ELECTROOPTIC EFFECT DEVICES (SEeDs)
(a)
573
(b)
R
+
~
V o == V + R I R
Output Light Pout
(c)
= T(V) Pin (d)
Pout == T(V) Pin B
H
o
:>P·in Figure 13.11. (a) ' A circuit diagram for a self-electrooptic effect device with a resistor load (R-SEED) in the presence of an incident laser light at the in pu t Pin ' (b) A graphical solution for the photocurrent response JR = S(V)Pin + Jo(V) and the load line Vo = V + RJR,' (c) The transmission reV) of the laser light passing through the MQW p-i-n diode is plotted as a function of the voltage drop V across the diode. (d) The switch diagram for the optical output power vs. the optical input power with the arrows showing the path of switching.
where V is the voltage drop across the diode. The reverse bias volt age V and the reversed current JR are defined as shown in Fig. 13.11a. For an incident .laser light with a power Pin, the Current JR is the sum of the photocurrent S(V)P in and the dark Current JD(V): ! ( 13.6.2) where S( V) is the responsivity of the diode and is defined as TJ int A
S(V) = q - fzw
(13 .6 .3)
where (13.6.4) is the absorbance, that is, the fraction of absorbed power for a unit incident power, assuming a single path absorption. The absorbance can be derived by noting that the reflectivity at the front surface R p , plus' the transmission after
574
ELEC·'i=(OABSORPTION MODULATOFS
passing through the substrate (I - R p )( ] - R,) e -aL, plus the absorbance A, must equal]. At steady state, the voltage drop across the multiple-quantumwell diode V and the current lR is determined by the simultaneous solutions of the above two equations. A graphical illustration of these two equations is plotted in Fig. 13.11b, where the intersection points stand for the possible solutions for I R and V. As can be seen from Fig. 13.11b, when the optical input power Pin is increased, the photocurrent is irtcreased , in general, and the number of intersection points varies. For an optical power equal to P.In, }, we have two intersection points A and E with corresponding voltages VA and VE . Therefore, there are two possible output states: PO U I = T(VA)P in, " which is higher in output power, and POU I = T(VE)P in l' which is lower in output power because of the transmissivity T(VA ) > r(VE ) (Fig. 13.llc). Once we increase the optical input power to Pin, 2' we find that there are three intersection points, B , D, and F, with corresponding voltages VB' VD , and VF . Therefore, the optical output powers through the diode are given by three possible values: Pout = T(VB)Pin, 2 > T(VD)P in, 2 > T(VF)P in, 2 ' Increasing the optical input power to P in , 3 , we have only two intersection points, C and G, with corresponding voltages, Vc and . Ve . Therefore , we obtain the output powers Pout = T(VC )P in, 3 > T(VC )P in , 3 ' The switching curve and the directions are shown in Fig. 13.11d. At a small input power, Pin < Pin, l' the optical transmission power Pout = T( V)?in is monotonically increasing with the input power P in' since the photocurrent is small for a small incident optical power. Therefore, most of the reverse bias voltage is across the diode and V is close to Va (VA < V < Va)' In this range of voltage, the transmission coefficient is rather flat or monotonic. As the input optical power exceeds Pin, l' P in. 2 , and P in, 3 ' photocurrent will appear in the circuit, and the voltage drop across the diode will drop from Vc to Ve , where the transmission will drop from a high value T(Vc ) to-a low value T(Ve ). After Pin> P i n , 3 ' the output power starts to increase again, since Pout = T(V)P in increases as Pin increases. This switch sequence is therefore A ~ B ~ C ~ G ~ H. In the reverse direction, if we switch down the optical input power from a large value of Pin at H, it will go through H ~ G ~ F ~ E ~ A ~ 0, since at point E the voltage has to switch from VE to VA as we decrease the input power Pin ~ Pin i- Therefore, the optical output power will switch from a low state E to a high state A due to the large transmission coefficient T(VA ) > T(VE ) ·
,
Symmetric self-electrooptic effect devices [53] (S-SEEDs) using another p-i-n multiple-Quantum-well diode as the load, and field-effect transistor self;.. electrooptic effect devices (F-SEEDs) [20] have also been demonstrated to show interesting physics and applications. For example, the S-SEED can act as a differential logic gate capable of NOR, OR, NAND, and AND functions. These devices made by maximizing the ratio of the absorption coefficients in the high and low states while minimizing "the change in electric
PROBLEMS
575
field can give nearly optimum performance [53]. .From the I-V curve of a SEED (Figs. 13.11a and b), we see that negative differential conductivity exists. A SEED oscillator [19, 52] can also be designed by a series connection of a SEED and an L-C resonator circuit and the SEED is optically pumped to produce a negative electric conductance in the photocurrent response. For example, oscillators with oscillation frequencies from 8.5 to 110 MHz have been demonstrated [52]. For the 8.5-MHz oscillator; frequency tuning by changing the bias voltage of the SEED has a tuning rate 16.7 kl-Izy V, This frequency tuning is caused by the change in the capacitance in the depletion layer of the SEED with the voltage change. The capacitance can also be changed optically by changing the optical power coupled to the SEED. PROBLEMS 13.1
In this problem, we use an alternative approach to show the physical interpretation of 21
For convenience, we use the normalized distance ! = r/ ao' the normalized wave number K = k r k ; = ka o ' and normalized energy § = E/R y = K 2 , where a o = 47TE s h 2/ m r e 2 is the exciton Bohr radius, and R y = m re 4 / 2 h 2 ( 4 7T E ) 2 is the exciton Rydberg energy. (a) Show that the solution is of the form
where YtmU~, cp) are the spherical harmonics as shown hydrogen atom case. R(!) satisfies
III
the .'
The solution is the .spherical Bessel function
(b) Show that R ld ( ! ) above satisfies the 8(K - K') normalization rule
57(,
EU.::.cCROAf)SORPTIO;\l MODULATORS
(c) Show that in physical units, the wave function can be written as
satisfying the 8(E - E') normalization rule
where E = K 2 R y = tz 2 k 2 j (2 m r ) has been used. (d) The wave function at r = 0 does not vanish only if t = O. The complete wave function is
Show that the wave function at the origin is
which is exactly the 3D reduced density of states, denoted by p:D(E).
13.2
Derive Eq. (13.1.13).
13.3
Plot the Franz-Keldysh absorption spectrum for GaAs with an applied field F = 100 kV/ ern at T = 300 K.
13.4
Compare the oscillation strengths and the exciton binding energies of the bound states of the 2D and 3D excitons.
13.5
Compare the absorption spectra of the continuum-state contributions of the 2D and 3D excitons.
13.6
(a) Show that for interband absorption in a pure two-dimensional structure without exciton effects, the absorption spectrum taking into account the finite linewidth broadening is given by
where E = (flw - Ec)/R y. (b) Carry out the integration analytically and plot the absorption spectrum a( PI w ).
REFERENCES
577
13.7
Derive 03.4.17).
13.8
Show that C(x) defined in 03.4.31) gives C(O) = 1 and C(co) = O.
13.9
Use' the perturbation result (13.4.52) for the band-edge transition energy E~~(F) to compare with the data shown in Fig. 13.7. Estimate the exciton binding energies for the heavy-hole and light-hole excitons separately. Discuss the accuracy of this simple method.
13.10
Compare the advantages and disadvantages of the waveguide modulator vs. the transverse transmission modulator.
13.11
Discuss the physics and operation principles of a SEED.
REFERENCES 1. W. Franz, Z. Naturforsch, IJ"3, 484 (1958).
2. L. V. Keldysh, "The effect of a strong electric field on the optical properties of insulating crystals," Soviet Phys, JETP 34, 788-790 (1958). 3. K. Tharmalingam, "Optical absorption in the presence of a uniform field," Phys. Rev. 130, 2204-2206 (1963~ 4. R. J. Elliot, "Intensity of optical absorption by excitons," Phys. Rev. 108, 1384-1389 (1957). 5. R. J. Elliot, "Theory of Excitons: I," pp. 269-293 in C. G. Kuper and G. D. Whitfield, Eds., Polarons and Excitons, Scottish Universities' Summer School, Plenum, New York, 1962. 6. R. S. Knox, "Theory of Excitons," in Solid State Physics, Suppl. 5, Academic, New York, 1963. 7. J. D. Dow and D. Redfield, "Electroabsorption in semiconductors: The excitonic absorption edge," Phys, ReL'. B 1,3358-3371 (1970). 8. E. J. Johnson, "Absorption near the fundamental edge," Chapter 6, pp. 153-258 in R. K. Williardson and A. C. Beer, Eds., Semiconductors and Semimetals, Vol. 3, Academic, New York, 1967. 9. J. O. Dimmock, "Introduction to the theory of exciton states in semiconductors," Chapter 7, pp. 259-319 in R. K. Williardson and A. C. Beer, Eds., Semiconductors and Semimetals, Vol. 3, Academic, New York, 1967. 10. T. H. Wood, C. A. Burrus, D. A. B. Miller, D. S. Chemla, T. C. Damen, A. C. Gossard, and W. Wiegmann, "High-speed optical modulation with GaAsjGaAIAs . quantum wells in a p-i-n diode structure," Appl. Phys, Lett. 44, 16-18 (1984). 11. D. A. B. Miller, D. S. Chemla, T. C. Damen, A. C. Gossard, W. Wiegmann, T. H. Wood, and C. A. Burrus, "Band-edge electroabsorption in quantum well structures: The quantum-confined Stark effect," Phys. Rev. Lett. 53,2173-2176 (1984). 12. D. A. B. Miller, D. S. Chernla, T. C. Darnen, A. C. Gossard,W. Wiegmann, T. H. Wood, and C. A. Burrus, "Electric field dependence of optical absorption near the band gap of quantum well structures," Phys. Rev. B 32, 1043-1060 (1985).
i
I:
i
I i'I~·
578
c LECTi{OABSORPTION MODULATORS
13. S. Schmitt-Rink, D. S. C hcrnla, and D. A. B. Miller, " Li ne ar and nonlinear optical properties of semiconductor quantum wells," Ado, Phys. 38 , 89-188 (1989). 14. M. Shinada and S. Sugano, "Interband opt ical transitions in extremely anisotropic semiconductors, I: Bound and unbound exciton absorption," I , Phys . Soc. Jpn , 21, 1936-1946 (1966) . 15. S. L. Chuang, S. Schmitt-Rink, D. A. B. Miller, and D. S. Chemla, "Exciton Green's-function approach to optical absorption in a quantum well with an applied electric field, " Phys. Re v. B 43, 1500-1509 (1990. 16. T. H . Wood, "Multiple quantum well (MQW) waveguide modulators," l. Lightwaue Technol. 6 , 743-757 (1988). 17. D. A. B. Miller, J. S. Weiner, and D. S. Chemla, "Electric-field dependence of linear optical properties in quantum well structures: Waveguide electroabsorption and sum rules," IEEE l. Quantum Electron. QE-22, 1816-1830 (I986). 18. D. A. B. Miller, D. S. Chemla, T. C. Damen, A. C. Gossard, W. Wiegmann , T . H . Wood, and C. A. Burrus, " Nove l hybrid optically bistable switch : The quantum well self-electra -optic effect device," Appl. Phys , Lett:.....45 , 13-15 (1984). 19. D . A. B. Miller, D. S. Chemla, T. C. Damen, T . "H . Wood, C. A . Burrus, A. C. Gossard, and W. Wiegmann, " T he quantum well self-electrooptic effect device: Optoelectronic bistability and oscillat ion, and self-linearized modulation, " IEEE l. Quantum Electron. QE-21, 1462-:1476 (1985 ). 20. D. A. B. Miller, M. D. Feuer, T . Y. Chang , S. C. Shunk, J . E. Henry, D. J. Burrows, and D . S. Chemla, "Field-effect transistor self-electrooptic effect device: Integrated photodiode, quantum well modulator and transistor," IEEE Photon. Technol. Lett . 1, 62-64 (1989). 21. D. E. Aspnes, " E lectric-field effects on the dielectric cons tan t of solids," Phys . Rev. 153, 972-982 (967). 22. D. E. Aspnes and N. Bottka, "Electric-field effects on the dielectric function of semiconductors and insulators," pp. 459-543 in R. K. Williardson and A. C. Beer, Eds., Semiconductors and Semimetals, Vol. 9, Modulation Techniques, Academic, New York, 1972. 23. M. Cardona, Modulation Spectroscopy, pp. 165-275 in Solid State Physics, Suppl. 11.~ Academic, New York, 1969. 24. B. R. Bennett and R. A . Soref, " E lectrore fraction and electroabsorption in InP, GaAs, GaSb, InAs, and InSb, " IEEE l . Quantum Electron . QE-23, 2159-2166 .' (1987). 25. D. A. B. Miller, D. S. Chemla, and S. Schmitt-Rink, "Relation between electrcabsorption in bulk semiconductors and in quantum wells : The quantum-confined Franz-Keldysh effect," Phys, Reu. B 33, 6976-6982 (1986 ). :26. H. Shen and F. H . Pollak, "Generalized Franz-Keldysh theory of electromodulation," Phys. Rev. B 42,7097-7102 (1990). 27. M. Abramowitz and I. A. Stegun, Handbook of Mathematical Functions , Chapter 10, Dover, New York, 1972. , 28. F. Bassani and G. Pastori Parravicini, Electronic States and Optical Transitions in Solids, Pergamon, Oxford , UK, 1975.
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5'!9
29. C. Y. P. Chao and S. L. Chuang, "Analytical and numerical solutions for a two-dimensional exciton in momentum space," Phys. Rev. B 43, 6530-6543 (1991). 30. M. D. Sturge, "Optical absorption of gallium arsenide between 0.6 and 2.75 eV," Phys. Rev. 127, 768-773 (1962). 31. J. S. Blakemore, "Semiconducting and other major properties of gallium arsenide," 1. Appl. Phys. 53, R123~R181 (1982). 32. G. Livescu, D. A. B. Miller, D. S. Chemla, M. Ramaswamy, T. Y. Chang, N. Sauer, A. C. Gossard, and J. H. English, "Free carrier and many-body effects in absorption spectra of modulation-doped quantum wells," IEEE l. Quantum Electron. 24, 1677-1689 (1988). 33. G. Bastard and J. A. Brum, "Electronic states in semiconductor heterostructures," IEEE l. Quantum Electron. QE-22, 1625-1644 (1986). 34. G. D. Sanders and Y. C. Chang, "Theory of photoabsorption in modulation-doped semiconductor quantum wells," Phys. Rev. B 35, 1300-1315 (1987). 35. R. Zimmermann, "On the dynamic Stark effect of excitons, the low field limit," Phys. Status Solidi B 146, 545-554 (1988). 36. Y. Kan, H. Nagai, M. Yamanishi, and 1. Suemune, "Field effects on the refractive index and absorption coefficient in AlGaAs quantum well structures and their feasibility for electrooptic device applications," IEEE 1. Quantum Electron. QE-23, 2167-2180 (1987). 37. M. Yamanishi and 1. Suemune, "Comment on polarization dependent momentum matrix elements in quantum well lasers," lpn. l. Appl. Phys, 23, L35-L36 (1984). 38. M. Asada, A. Kameyama, and Y. Suematsu, "Gain arid intervalence band absorption in quantum-well lasers," IEEE 1. Quantum Electron. QE-20, 745-753 (1984). 39. B. Zhu and K. Huang, "Effect of valence-band hybridization on the exciton spectra in GaAs-Ga I-.x Al x As quantum wells," Phys, Rev. B 36, 8102-8108 (1987). \ 40. G. E. W. Bauer and T. Ando, "Exciton mixing in quantum w~lls," Phys, Rev. B 38, 6015-6030 (1988). 41. H. Chu and Y. C. Chang, "Theory of line shapes df exciton resonances semiconductor super lattices," Phys. ReL'. B 39, 10861-10871 (1989).
10
42. L. C. Andreani and A. Pasquarello, "Accurate theory of excitons GaAs-GaI_xAlxAs quantum wells," Phys, Rev. B 4-2, 8928-8938 (1990).
10
43.
c. Y. P. Chao and S. L. Chuang, "Momentum-space solution of exciton excited states and heavy-hole-light-hole mixing in quantum wells," Phys. Rev. B 48, 8210-8221 (1993).
44. M. Matsuura and T. Kamizato, "Subbands and excitons in a quantum well in an electric field," Phys. Rev. B 33, 8385-8389 (1986). 45. G. Bastard, E. E. Mendez, L. L. Chang, and L. Esaki, "Variational calculations on a quantum well in an electric field," Phys. Rev. B 28, 3241-3245 (1983). 46. S. Nojima, "Electric field dependence of the exciton binding energy in GaAsj AlxGa1_xAs quantum wells," Phys. Rev. B 37,9087-9088 (1988).
I,
580
ELF,CTROABSORPTION MODULATORS
47. D. Ahn and S. L. Chuang, "Variational calculations or subbands in a quantum well with uniform electric field: Gram-Schmidt' orthogonalization approach," Appl. Phys. Lett. 49, 1450-1452 (1986). 48. J. S. Weiner, D. A. B. Miller, D. S. Chemla, T. C. Damen, C. A. Burrus, T. H. Wood, A. C. Gossard, and W. Wiegmann, "Strong polarization-sensitive electroabsorption in GaAsjAIGaAs quantum well waveguides," Appl. Phys, Lett. 47, 1148-1150 (985). 49. P. Lefebvre, P. Christol, and H. Mathieu, "Unified formulation of excitonic absorption spectra of semiconductor quantum wells, superlattices and quantum wires," Phys, Rev. B 48, 17308-17315 (1993). SO. H. S. Cho and P. R. Prucnal, "Effect of parameter variations on the performance of GaAsjAlGaAs multiple-quantum-well electroabsorption modulators," IEEE J. Quantum Electron. 25, 1682-1690 (1989). 51. G. Lengyel, K. W. Jelley, and R. W. H. Engelmann, "A semi-empirical model for electroabsorption in GaAs / AlGaAs multiple quantum well modulator structures," IEEE J. Quantum Electron. 26, 296-304 (1990). 52. c. R. Giles, T. H. Wood, and C. A. Burrus, "Quantum-well SEED optical oscillators," IEEE J. Quantum Electron. 26, 512-518 (1990). 53. A. L. Lentine, D. A. B. Miller, L. M. F. Chirovsky, and L. A. D'Asaro, "Optimization of absorption in symmetric self-electrooptic effect devices: A system perspective," IEEE J. Quantum Electron. 27, 2431-2439 (1991). 54. P. J. Mares and S. L. Chuang, "Comparison between theory and experiment for InGaAs / InP self-electrooptic effect devices," Appl. Phys, Lett. 61, 1924-1926 (1992). 55. P. J. Mares and S. L. Chuang, "Modeling of self-e lectrooptic-effect devices," J. Appl, Phys. 74, 1388-1397 (1993). 56. M. K. Chin and W. S. C. Chang, "Theoretical design optimization of multiplequantum-well electroabsorption waveguide modulators," IEEE J. Quantum Electron. 29, 2476-2488, 1993.
PARTV Detection of Light
.-
,I
14 Photodetectors Photodetectors play important roles in optical communication systems. The major physical mechanism of photodetectors is the absorption of photons, which changes the electric properties of the electronic system, such as the generation of a photocurrent in a photoconductor or a photovoltage in a photovoltaic detector. The performance of a photodetector depends on the optical absorption process, the carrier transport, and the interaction with the circuit system. For intrinsic optical absorptions, such as interband processes in a direct semiconductor, the general theory for the absorption spectrum has been presented in Chapter 9. The interband absorption creates electron-hole pairs. The carrier transport of these electrons and holes after generation depends on the design of the photodetectors. In this chapter, we study photoconductors, photodiodes using p-n junctions and p-i-n structures, avalanche photodiodes, and intersubband quantum-well photodetectors. Our focus is on the understanding of the physical processes of the carrier generation and transport. We derive the relation between the optical pr .er and the photocurrents. Some important noises in these photodetectors are also discussed. More extensive treatment of photodetectors can be found in .' Refs. 1-~. I
\
14.1
PHOTOCONDUCTORS
.'
14.1.1
Photoconductivity
Consider a uniform p-type semiconductor with a uniform optical illumination. The total electron and hole carrier concentrations, nand p, deviate . from their thermal equilibrium values, no and Po, by the excess carrier i concentrations, on and op, respectively, due to the optical excitation: n = no
+ on
p = Po
+
Bp
(14.1.1)
Since Po » no in an extrinsic p-type semiconductor, the net thermal recombination rate (2.3.14) can be reduced to
R':" n
=
on
(14.1.2) , 583
PHDTODETECIORS
------.~
E
-~--~---~---i ..-. D--?
Hole
I
.........
d
Electron!
+~ 111-_------------'
L..-
V Figure 14.1.
A simple photo conductor with an external bias voltage V.
where the low-level injection condition, on,op «Po, has been assumed. Thus the electron concentration will satisfy the rate equation a'6
-n=G at a
on
(14.1.3)
where Go is the net optical generation rate. For a uniform semiconductor with a de voltage bias V, as shown in Fig. 14.1, the electron and hole current densities are given by only the drift components, since there is no diffusion current due to the lack of spatial dependence (a/ax == 0): (14.1.4) The total current density is \ ( 14.1.5) where the conductivity is a
= q(ILnn + ILpP)
( 14.1.6)
The photoconductivity 6u is defined as the difference between the conductivity when there is an optical injection and the dark conductivity u o: 6u = a Uo
=
U
o = q(ILn
on
q(ILnn o + J-LpPI))
+
J.1 p 8p)
(14.1.7) ( 14.1.8)
The total current I is the current density J multiplied by the cross-sectional
14.1
PHOTOCONDUCTORS
585
area A = wd. I
fA
=
=
aEA
oAV =
(14.1.9)
t
where the electric field E = V/ t ,with t the length of the sample, has been used. The photocurrcnt 6.1 is defined as the difference between the total current in the presence of optical excitation and the dark current 10 = O"oAV/t. (14.1.10)
14.1.2
Photocurrent Responses in the Time Domain
Case 1: A Constant Light Intensity. If Go is independent of time, a/at at steady state, we obtain
=
0
(14.1.11) and op = on, since each broken bond creates one electron-hole pair. Thus, the photocurrent is given by
6.1
=
q(ILrr
+ IL p ) G o7
AV
ne
=:::
QJLn G o7
AV
ne
(14.1.12)
since usually J-L n » J-L p ' The above expression can also be expressed in , . ..rrns of the transit time of the electrons: , \
7/ =';
such that
.-
t
v;
-
t J-LnE
-
t
2
(14.1.13)
ILnV
!
(14.1.14) The above expression has a good physical interpretation. The term Go t A is the total number of electron-hole pairs created per second in the sample with a volume tA., The ratio 7 n/7/ gives the photoconductive gain, which is determined by how fast the electrons can transit across the electrodes and contribute to the photocurrent in the circuit before they can recombine with holes. As shown in Fig. 14.1, when an electron-hole pair is created, the photocurrent will be small if the electron and the hole immediately recombine before they can be collected by the electrodes (i.e.; the recombination
. . ...~,. .""":",.. ~ ""T"",.,....'7"" ....-. .,...~- ~ ................ - ~
~."fOo' ... ~ - ( t" _ ..•.,.- . - .... ...-. ' .- ... . . . _ -- .....
.. _ '~ -- -. • : . ... .
-.o:"........... ~ '"'::""••••
.... .
..,...
~~tJ:f:"!
t'" '~~•• ,~; .....,' ~
...~ -,':~•• \\":! .. ~ ~~t:"-:!'F'~~
PI-lOTOD ETEcrOR~;
586
lifetime T lI is much s ho rte r than the transit time). On the other hand, when the transit time T( is short, a significant number of photogenerated electrons will be able to reach the left electrode before they recombine with holes in the semiconductor. To preserve ch arge neutrality in the semiconductor, the left electrode will provide the same number of holes at the same rate as the electrons reaching that electrode per second , resulting in th e photoconductor current measured by the external circuit. For example, Tn I T( = 10 is equiva lent to having ten round-trips taken by the electron before it disappears by recombination in the photoconductor. The optical generation rate is equal to the number of injected photons per second, or photon flux (Po p t I hv') per unit volume (fwd) multiplied by the quantum efficiency T} : Go =
Po P t I h v T}
------'t w-d-
...... .:' ' .,..
:- j.....I'1'. ~._.-_
(14.1.15)
where w is the width, d is the depth of the sample ( wd = A), P o P t is the optical power (W) of the injected light, and 7] is the quantum efficiency or the fraction of photons creating electron-hole pairs. If the surface reflections and the finite thickness of the detector are considered, the quantum efficiency T} is just the intrinsic quantum efficiency 7] j multiplied by the absorbance derived in (5.3.51):
(14.1.16) where R is the optical reflectivity between the air and semiconductor, an d a is the absorption coefficient of the optical intensity. The injected primary photocurrent I ph is defined as
(14.1.17) The photocurrent is
(14.1.18) Again th e photoconductive gain is given by
(14 .1.19) If there are more electrons traveling across the electrodes before recombining with the holes, there will be more photocurrent appearing in the external circuit. The current responsivity R ). (AI ltV) is the photocurrent response per
.~.
14.1
PHOTOCONDUCTORS
587
unit optical incident power (14.1.20) and depends on the operation wavelength A. Case 2: Transient Response. If the constant light illumination is switched off at t = 0, that is, Go(l) = Go, t < 0 and 0 for t > 0, the response for t > 0 will be
a
-on(t)
on( t)
at
(14.1.21)
or
(14.1.22a) and the photocurrent response obtained from (14.1.10) or (14.1.12) is (14.1.22b) The result is shown in Fig. 14.2a. The decay time constant is the minority carrier recombination lifetime 'Tn. If the light injection is an impulse function, (14.1.23) Then,
a
-
at
on(t)
=
go o(t)
one t)
(14.1.24)
Integrating the above equation from t = 0 _ to 0 + will give
Assuming that initially on(O_) = 0, that is, the semiconductor is at thermal equilibrium before t = 0, and the excess carrier concentration is zero, we obtain for t > 0 This result is plotted in Fig. 14.2b.
( 14.1.25)
PHOTODETF CTORS
(a)
8n(t)
o
o (b)
(c)
Ga(t)::= Go (1 + m co s cot)
----.----i---.---r-l~wt
-T[
o
- - - - - i f - L . . - - - - -__ Wt
rt
Figure 14.2. The generation rate G oCt} and the excess carrier con centration Sn(t} for (a ) swi tch-off, ( b) impulse respon se , and (c) sinu soidal s teady-sta te response of a photo conductor.
Case 3: Sinusoidal Steady-State Response. If the optical intensity is modulated by a sinusoidal signal such that
.-
C o( t)
=
Cocos
( 14 .1.2 6)
co t
the sinusoidal ste ad y-s ta te re sponse can be found by letting I
(14.1.27)
on(t) = Re(on e- i W I ) wh ere Re me ans the real part of the follow ing quantity. W e have
a one t) -on(t) = Cocos wt-
at
Using G o cos cot
Re (G n e -
(14.1.28)
Tn
iw
{) ,
Bn
we o bt a in =
( 14.1.29)
Id .l
PhOTOCONDUCTORS
589
Thus
(14.1.30)
where ¢ = tan -l(WTn ) is the phase delay in the ac response. On the other hand, if the optical intensity or the optical generation rate consists of a de and an ac component,
+ m cos
Go (t) = Go (1
(14.1.31)
wt)
where m is the modulation index, the response of the excess carrier concentration will be (14.1.32) where ¢ is the same as in (14.1.30), The above results are shown Fig. 14.2c. Using (14.1.15)-(14.1.17), we find that for an optical input power P ( t)
=
+ m cos
Popt (1
In
(14.1.33)
wt )
the photocurrent response is
let) = lp[l +..; 1 +m
.2
W
2 Tn
cos(wt -
POP! Tn
I p
!
= qTJ--
hv
T
>l]
\I I,
(14.1.34a)
(14.1.34b)
/
In other words, for a root-mean-square (rrns) optical power of which we replace the cosine function by 1/ Ii , (14.1.35)
P rm s =
the rms photocurrent signal is 1.
P
=
rm s
P - ( -t: qTJ hv Tt
J -,=.====-
(14.1.36)
.
I
,
590
14.1.3
PHOTODETECTORS
Noises in Photoconductors [6]
In this subsection, we present some fundamental concepts including the spectral density function for noises in photodetectors. Important noises such as generation-recombination or shot and thermal noise are discussed. Spectral Density Function SCI). The signal such as the photocurrent in the time domain i(t) of the photoeonductor is related to its Fourier transform i( f) in the frequency domain by
/'IJ i(f)e-
i(t) =
i27T / t d f
(14.1.37a)
-00
i(f)
Joo i(t)e
=
i 2 rr t /
dt
(14.1.37b)
-00
The average power P over a time duration T is
1 T / 22' 1 P=-! i (t ) dt = - J T
T
-T/2
li(f)1 df -00
2 -T 1 Ii (o f ) df 1 S(f) df o 00
=
2
00
00
2
1
=
(14 .1.38)
where we have used
lim
JT/2 e
T-HO
-T/2
i2Tr(f-f')r
dt
= 8 (f - f')
and defined the spectral density function St f
(14.1.39 )
) as
2 2 S(f) = T1i(f)1
( 14.1.40)
Shot Noise. For a sequence of events such as collection of charges within a time interval T, say ~
L
i( t) = i
=
h( t -
tJ
cs i « r
(14.1.41)
1
where N, = total number of events within time T, we obtain the -Fourier transform ief): NI
i( f)
2: h( f)exp(i27T ft i=l
j )
( 14.1.42)
i4.1
PHOrOCONDUCTORS
591
The ensemble average of Ji( f )J2 is 2
(Ii(/) 1)
~ (lh(/) 1{N,-/- i~ ~ exp[i27rf(t t,)]}) 2
j -
=
Ih(f) 12( ~ )
(N)Tlh(f)
=
2
(14.1.43)
1
where (N) = (Nt)/T is the average number of events occurring per second. The random distributions of t , and t j give the cancellation in the second term in (14.1.43) when i =1= j. The spectral density function is (14.1.44) Now we consider an inj ected electron between two capacitor plates with a separation f . The current is q
h(t)
=
- vet)
(14.1.45)
f
where uCt) is the instantaneous velocity of the ele ctro n and T t is the transit time. The average current ( I) is related to the average number of electron injections per second ( N) by (I )
q (N )
=
(14.1.46~
The Fourier transform of h(t) reduces to .'
h(f) =
jT,q u ( t ) e i2-rr f t d t ::::; fq o f
assuming the frequency density funct ion is
S(f)
=
IS
f
dx(t) dt dt
=
q
( 14.1.47)
low enough such that fT t « 1. The spectral I
2
2(N ) lh (f) 1 = 2(N )q 2 = 2q (/ )
( 14 .1.48 )
The power of this shot noise within a frequency interval between f + 6.f associated with the current is denoted by
(iHf»)
=S(f)6./
=
2q(/ )6.f
f
and
( 14.1.49)
Generation-Recombination Noise. In a photoconductor, the photogenerated carriers have a finite lifetime T , which is a random variable with a 'mean value ( T ) denoted as Tn for, . _the .. • electrons. The photocurrent due to 'On e injected
PHOTODETECTORS
592
electron is O:s;t:S;T
( 14.1.50)
otherwise Here we use u as the mean drift velocity and time. The Fourier transform of hCt) is h( [) =
foT
q
ei 27Tfl_
Tl
t/
=
lJ
as the mean transit
q (ei2 rrjT - 1 dt = - - - . - -
Tl
1
I21T[
Tl
(14.1.51) If we assume that the probability function of the random variable
T
obeys
Poisson statistics ( 14.1.52) with an average
=
JOT p( T) d-r =
Tn'
we find
( 14.1.53) Since the average photocurrent with the photoconductive gain
1p == (I) =
Tn
IT
l
due to
(14.1.54)
1
the spectral density function due to
( 14 .1.55)
The generation-recombination noise current is, therefore,
(ibR )=S([)Llj=
4q/(T /T)Ll[ p
1
n
(
+ (21T[1",;)
2
(14.1.56)
14.1
PHOTOCONDUCTORS
593
Thermal Noise (also Johnson Noise or Nyquist Noise) [6-8]. In a photodetector, the random thermal motion of charge carriers contribute to a thermal noise current. In other words, the thermal noise of a resistor R results in a random electric current i(t), which is characterized by a power spectral density at temperature T: 4 5(/) - R
hf eUI!/kaT) -
(14.1.57)
1
This thermal noise current adds to the photocurrent signal i /t) and affects the clarity of the detected signals. At low frequency hf « k BT, we have
S(f) -
(14.1.58)
The thermal noise is described by
(i})
=
1a si r, df = 4k RTts ] ~!
_ B_ _
( 14.1.59)
where the bandwidth /).f of the circuit is assumed to be much smaller than kBTlh. Signal-to-Noise Ratio. The power signal-to-noise ratio is therefore [8] Y]m 2 ( Po p t I hv) 8/).f[1 + (k BTlqRJp
)(Tt I Tn )(l + W 2 T: )] ( 14.1.60)
Noise-Equivalent Power (NEP). The noise-equivalent power is defined as the power that corresponds to the incident rms optical power (P r m s = m PoPt Iii) required such that the signal-to-noise ratio is one in a bandwidth of 1 Hz. Detectivity (D *). The detectivity is defined as
D*
=
{Ab:7 em (HZ)1/2 IW NEP
(14.1.61)
where A is the detector cross-sectional area in crrr'. More discussions on photoconductive detectors such as Hg .Cd I-xTe can be found in Ref. 9.
~
•. . . . ••. • •._', ~
~
_._,y . _
~
-
~"
"
"
"" ""'- " - ---'--- ' .-
•
. - - - _.
,
594
14.1.4
. -- ~ ~
·· ~ ~ ·/"'..-.-r' '''
' - ,-••
_ . , .~
• '_.-
PHOTODETECTORS Il-l-P-l
Superlattice Photoconductor [10, 11]
Recently, modulation doping in semiconductors has been introduced for novel device applications. An interesting example is a GaAs doping superlattice used as a photoconductor. For an extensive review of the compositional and doping sup e rlat t ice s, see Refs . 10 and ] 1. Here we consider a GaAs doped periodically n-type and p-type separated by intrinsic regions as shown in Fig. 14.3a. The electric field profile Et.z') can be obtained by noting that dE(z)/d z = p(z)/e , where p(z) = +qND in the n-doped regions, -qNA in the p-doped regions, and zero in the intrinsic regions. Th erefore, E(z) is either a linear profile with a positive slope qND / e in n regions, a negative slope -qNA /e in p regions, or a zero slope in the intrinsic regions (Fig. 14.3b). The potential profile for the conduction band edge Ec(z) = -qcp(z) = +qf~ooE(z')dz' is the integral of the electric field profile and is shown in Fig. 14 .3c . For an incident light with energy above the band gap, the photogenerated carriers will fall to the band edge and will drift or diffuse to the valleys of (a) Charge density p(z) +qN O
.........
+qN D
E
~
n
-E
i
p
i
-
-qN A
+qN n
E
n
i
E
p
i
E
- f-.n
z
-qN A
(b) Electric field E(z)
---r---~:-----:f----+---I---~z
(c) Energy band diagram
Figure 14.3. (3) The charge dens ity profile due to ionized donors and acceptors in an n-i-p-i doping superlattice using the depletion approximation . (b) The e lectric field profile due to the ch arge distribution in (a). Notice that the electric field E = 2E(z) is alternating between positive and negative di rections. (c) The energy band diagram of the n-i-p-i superlattice. The photogenerated electron -hole pairs are separated in real space because of the band profiles.
14.2
p-n
JUNCThJN PHOTODIODES
595
each band, as shown in Fig. 14.3c. The electrons arc separated from the holes in real space, resulting in a very long recombination lifetime Tn' This enhancement of a long lifetime has been found to be many orders of magnitude larger than the bulk carrier lifetime. Since the photocurrent response is proportional to CaT,l' an extremely large responsivity using the n-i-p-i superlattice as a photoconductor can be designed.
14.2
p-n
JUNCTION PHOTODIODES [12-15]
Consider a p-n junction photodiode as shown in Fig. 14.4a. The charge distribution p(x), the electric field Ei;x ) and the potential energy profile under the depletion approximation have been discussed in Chapter 2. Here we investigate the photocurrent response if the diode is illuminated by a uniform light intensity, described by a generation rate C(x, t ), which is the number of electron-hole pairs created per unit time per unit volume. Let us focus on the n stele of the diode. The charge continuity equation is given by (2.4.2)
aPn at
oPn
=
C(x,t) - -
.
Tp
1
a ax
- - - J (x) q
(14.2.1)
p
(a) A p-n junction photodiode
f I
II r-
p
n
r--
'I'l (b) Charge density
p(x) tqN D
+ +
+
----....,.;.ti-l.----+- x
(c) Electric field x
Figure 14.4. (a) A p-n junction diode under the "illumination of a uniform light. (b) The charge distribution p(x) under depletion approximation. (c) The electric field Et x) obtained from Gauss's law.
590
PHOTODETECTOlZS
where P" = Pno + op" is the total hole concentration in the n region, PnO is the hole concentration in the absence of any electric or optical injection, and oP n is the excess hole concentration due to the external injections. The minority (hole) current density in the quasi-neutral region (x ;;::: xn) is dominated by the diffusion component [12-14], as discussed in Chapter 2:
(14 .2.2) Since PlIO is independent of x and t, we have at steady state, if G( x , t ) = Go is independent of x and t,
(14.2.3) The above equation can be solved by summing the homogeneous and particular solutions:
(14.2.4 ) homogeneous solution
particular solution
where L p = jDpTp is the diffusion length for holes. The particular solution is due to the optical generation. If the n region is very long, we can set C z = 0; otherwise , oPn(x ----7 00) ----) +00, which is unphysical. We expect as x ----) +00 that oPn(x) will approach GOTp = total photogenerated holes. At x = xn' the hole concentration is pinned by the voltage bias V with the exponential dependence
( 14.2.5)
if the Boltzmann statistics are assumed. Therefore, we obtain ( 14.2.6) and
The current density Jp(x) is
= q ~p [Pno( eqv/kBT p
-
1) _. GOTp ] e -' (x-x n ) / L
p
( 14.2.8)
H.2
P-Il JUNCTION
1 HOTOnIODES
59~·
We obtain J/x) at the boundary of the depletion region
D
Jp ( x n ) -- q ~ L Pl10 (qV/kBT e
-
Xn
as
1) - q G 0 L p
(14.2.9)
p
where the first term is due only to the voltage bias, and the last term is due to optical generation. We see that only that portion of the photogenerated holes within a diffusion length L p away from the depletion boundary can diffuse (and survive) to the depletion region and be swept across the depletion region by the electric field and collected as the photocurrent by the external circuits. This means that the majority of the carriers on the p side have to supply this current immediately. A parallel (or dual) approach for the electron current density at x = -x p gives
(14.2.10) The total current I is the sum of J/x n) and JnC - x p) multiplied by the cross-sectional area of the diode A:
I=A[Jp(x n ) + In(-x p ) ] =
I o ( eqV/kBT
-
1) -
qAG o ( L p + L n )
(14.2.11)
where
(14.2.12) I
is the diode reverse current. The last term, -iqAGo(L p + Ln>, is the photocurrent of the diode, which is proportional to the generation rate of the electron-hole pairs, G. The I-V curves of ?l photodiode with and without the illumination of light are plotted in Fig. 14.5. When Go = 0, the diode reverse
-------::r---/L........,;.,.------.v f-
Io(eqVIkBT-l)-qAGo(Lp+ L n)
With light Figure 14.5.
The I-V curves of a photodiode with and without illumination.
PHOTODETECTORS
598
current - l ois the dark current , whi ch is usually very small compared with the photocurrent I pl1 = - qA Go( L p + L,) under a reverse bias condition. Therefore, the photocurrcnt is proportional to the generation rat e G o, wh ich is proportional to the incidcn t optical power P o p t ' The problems with the p-n junction photodiodes are as folJows: 1. Optical absorption within the diffusion lengths L p and L" is very sm all , that is, over narrow regions of L p and L; near the depletion region. Since L p and L" are very sm all , the contributions of the photocurrents are not effective. 2. The diffusion process is slow, which results in a slow photoresponse if the optical intensity varies with time . 3. The junction capacitance C , is sim ply cA /x w ' where X w is the total depletion wid th derived in (2.5.24) sim plified for a hornojunction diode with c p = CN = e :
( 14 .2 .13) whi ch can slow down the response by the RC~ time delay. For example , if A = (l mm)2, e = l 1.7co , N D = 10 15 cm : «NA fo r a p+-n photodiode , and - V = 10V » Vo, we obtain Cj = 30 pF and the 3-dB cutoff frequency f 3d B = 1/(27TRC j ) = 100 MHz for R = 50 n . RoA Product [15]. A useful figure of merit for the p-n junction photodiodes is the RoA product. Since the photodiode is operated at zero-bias voltage in many direct detection applications, the differential resistance at zero-bias voltage R o multiplied by the junction are a A is commonly used: (RA) o
-1
d/l
dJI
1 =-- . -A dV v =o - dV
.
V=Q
iI
\
(14.2.14)
So far, we have derived the dark cu rre n t 10 contributed by the diffusion processes in thi s se ctio n. Us ing (14.2.11 ) and (14.2.12), we obtain
(14. 2.15 )
.. '
14.7.
!J-Il
JUNCTION PHOTODIODES
599
where we have used the relations Pno = NDln;, npo = NA In;, and the Einstein relations Dpl/-Lp = Dili/-Ln = kBTlq. The first term in 04.2.15) is the contribution to 1/(R oA) from the diffusion current on the n side of the photodiode,. and the second term is from the diffusion current on the p side. There can also be other contributions to RoA products, such as the generation-recombination current in the space-charge region, the surface leakage current, and the interband tunneling current, which depend on the material properties, device geometry, and surface conditions. For a root-mean-square photon flux density
(14.2.16) where A is the photodetector illumination area,
1.\
I~I
Ii
R
'» PI.
q
=-=7]A
hv
r~ r: i' ",
( 14.2.17)
The signal-to-noise ratio SIN (current) is
S
( 14.2.18)
N
The detectivity for the above SIN is defined as.'
(14.2.19)
For a photodiode at thermal equilibrium (i.e., no externally applied voltage and no illumination of light), the thermal noise depends on the zero bias resistance R o using (14.1.59): (i~) -
• ( 14.2.20)
PHOTODETEC1'ORS
600
When not in thermal equilibrium, the I-V curve is I( V) = I o ( e ( q VjkaT)
Iph =
-
1) - 1 ph
(14.2 .21)
Q7]cfJ n A
(14.2.22)
where ep n is the photon flux density due to the background radiation. The mean-squared shot noise current has contributions from three additive terms [15]: (1) a forward current, which depends on voltage, 10 exp(qVB/knT), (2) a reverse diode saturation current, and (3) the background radiation induced photocurrent. Since these shot noise currents fluctuate independently, the total mean-squared shot noise curr e n t is
(14.2.23 ) At an operation voltage V = 0, R 0 1 = (dI/dV) v=o can be wri tt en as
=
qlo /kBT and 04.2.23)
(14 .2.24) The detectivit y at zero bias voltage is then obtained from 04.2.19)
(14.2.25)
For a thermally limited case , i.e., when the thermal noise is dominant over the background radiation induced signal and other noises, we have
~ 14.2.26)
whi ch re lates th e R oA product to the th ermally limited detectivity. If the photodiode is ba ckground radiation lim ite d, which means that the background radiation-induced photocurrent is dominant, we have ( D A* ) BUP -_ _h1v
!
!
7J_ 2B
(14.2.27)
which is the detectivity of the background limited infrared photodetector (BLIP).
14 .3
14.3
601
p-i-l' Pl-IOTODIODES
p-i-n
PHOTODIODES [8]
To enhance the responsivity of the photodiode, an intrinsic region used as the major absorption layer is added (Fig. 14.6a). For a light injected from the p + side with an optical power intensity Jo p t (W/ ern"), the generation rate is
(14.3.1 )
G(x)
The optical power intensity Jo p t is the incident optical power PoPt divided by the area A (Jo p t = Popt / A). Note that the total injected number of electrons
(a)
x=Q
x=W n
Optical power (b)
L
t I
p(x)
+<jNo
0-----9
'-------+ )
x
-qN A E(x)
(c)
i
= JX p(x) dx'/E o
.t
", 'I
-00
(d)
(e)
(f)
~(x) =-~~(X') dx' -______:~;
~
-;.1_I;
X
~----.L----__.)
o
G(x)
w
= Optical generation rate = G o e-ax G 0 -- Tli I opt ( l-R)/hv x
Figure 14.6. (a) A p-i-n photodiode under optical illumination from the p + side, (b) the charge density p(x) under depletion approximation, (c) the static electric field profile Ei.x), (d) the electrostatic potential cp(x), (e) the conduction and valence band edge profiles, and (f) the optical generation rate G(x). .
.,,
PHOTODEfECfO!<..S
602
per unit area per second is
So
oo
=
fo
G(x) dx
lOPl
=
(1 - R)"7;hv
(14.3.2)
where lOPl / h v is the number of photons injected per unit area per second, and "7i is the internal quantum efficiency for the probability of creating an electron-hole pair for each incident photon. The energy band profiles for the p-i-n diode can be obtained graphically based on the well-known depletion approximation, as shown in Figs. 14.6b-e for the charge density p(x), the electric field Et x), the potential cjJ(x), and the band diagram. At steady state, the total photocurrent consists of both a drift and a diffusion current: (14.3 .3) Considering the p + region to be of negligible thickness, we look at the contribution in the intrinsic region-O < x < W:
(14.3.4) where the minus sign accounts for the fact that the draft current flows in the -x direction. The above expression also shows that an increase of W» 1/ a enhances the photocurrent because of the increasing amount of absorption. For x > W, the analysis is similar to that of the p-n junction diode, where the hole (minority) current density on the n side is due only to diffusion:
a
er; at
0=
J diff = -qDp-Pn(x) ax 8Pn 1 a =G(x)- "» q-axJp(x)
(14.3.5) (14.3.6)
Therefore, we solve
1 - --G(x) Dp
(14.3.7)
The solution for 8Pn(x) consists of the homogeneous solution and the particular solution 8P
rt
(
x) = Ae -(x- W) /L l' + Ce -{xX '--- - ~ - - -
... ~
homogeneous solution
particular solution
( 14.3.8)
lid
p-i-n PHOTODIODES
603
and we have discarded the term e +(x- W)/L p in the homogeneous part since oP,/x ~ co) should be finite. C is contributed by G(x) and is obtained by substituting Ce -ax into (14.3.7): (14.3.9)
The coefficient A is then determined by the boundary condition
oPn (W)
=
PnO (eqV/kBT
-
1) =
-PnO
(14.3.10)
which is pinned by the reverse bias voltage. Therefore,
A
-Pn O
=
-
Ce- a W
(14.3.11 )
and (14.3.12)
The hole current density on the n side is
J diff
d
= -
qDp - Pn ( x) dx
~
qD a(1 -
=
-
_1_)C
p
q
a
(
x=W
Lp
1
e- aw _ qDp P Lp
SoaL p e- aw + P
1 + aLp
Dp
nOL
nO
'J
(14.3.13)
p
The total current density is
(atx=W)
J=Jdr+Jdiff
~ -qSo( 1 -
1
:-::J -
qPno
/
~:
(14.3.14)
The quantum efficiency is aW
77
=
J/q Iopt/hv
=
77i(1-R)(1 -
e1 + aLp
1
(14.3.15)
neglecting the contribution of the diffusion term m (14.3.14). Note that if W ~ co, the current density is dominated by .l
=
-qSo
(14.3.16)
, .•
' ", ~
• •'- '
..,
,..,...
";.". . _
.
~
••• ,
0".••, ' " • ._
•. ,.
•• ., -
, ' , ""
' _.
- • ..'
PHOTODETECTOR~
604
and 17 = 77;C1 - R) as; expected. Long-wavelength p-i-n photodiodes for high-speed receiver applications are of gre at interest for optical communication systems. For high-sensitivity optical receivers, photodiodes with a small junction area around a few tens of microns in diameter and a low doping depletion region of a few microns are desired [16]. At low doping, the center absorption region can be depleted at a small bias voltage and reduce the tunneling leakage current. Most of the long-wavelength photodetectors use In0.47Gao.53As grown on an InP substrate as the absorption region. The leakage current in InGaAs p-i-n diodes is dominated by the interband tunneling at high reverse-bias voltages and generation-recombination processes at low voltages [17, 18]. Hybrid p-i-n / FET receivers have been assembled for high-speed photoreceivers, which offer better sensitivity than other p-i-n photodiode receivers [16, 19]. Ultrawideband p-i-n photodetectors have also been shown to have a great potential for high-speed applications [20] with an impulse response in the picosecond scale.
14.4
AVALANCHE PHOTODIODES
To enhance the photocurrent response, some built-in multiplication processes may be utilized such that more photocurrents can be extracted in the external circuits at a given optical illumination. Ideally, we would have a single carrier-type photomultiplier; the carrier concentration will grow if impact ionization occurs in a region with a large electric field. In semiconductors, both electrons and holes can impact ionize more electron-hole pairs, as sh own in Fig. 14.7a. A schematic diagram for an avalanche diode is shown in Fig. 14.7b. A feedback process occurs since electrons and holes travel in
hv~ I
•I I I
I I
o
~
Jp(W)
w
hv
>x
Hole injection
Figure loot? (a) The energy band diagram for an avalanche photodiode with the electron and hole ionization coefficients an and (3p. The electron and hole i nje cti ons are given by 1)0) and fpC W) . (b) A schematic diagram for an aval anche photod iode .
14.4
AVALANCHE PHOTODIODES
605
opposite directions. Let us define the electron ionization coefficient (l / em) = the number of electron-hole pairs generated by one incident electron per unit distance f3 p = the hole ionization coefficient (I / em) = the number of electron-hole pairs generated by one incident hole per unit distance
an
=
In general, an =I=- f3 p for most semiconductors. They are functions of the applied electric field E with an exponential dependence: 'i
.r:
where the constants ao, {3o, Cn' and C; depend on the materials. For a general overview of the fundamentals of -avalanche photodiodes, see Refs. 21-23.
14.4.1 Ideal Avalanche Photodiode-Single Carrier Type Capable of Ionizing Collisions [22]
We now consider the special case in which only electrons can impact ionize. Suppose we have an incident current density J/x) at a plane located at position x (Fig. 14.8a). Over an incremental distance L1 x, the total generated electron-hole pairs is a nL1x multiplied by In(x), since a nL1x is the number of ionized electrons per incident electron in a distance Li x. Therefore, the current density In(x + L1 x ) is the sum of the incident (or primary) current density and the ionized (or secondary) current density: (14.4.1)
(a) Electron impact ionizations only In(X)
Jp(X)
I
~
..-7 ..-7 e-7
~
~
~
~
~
H
I
I I
Ifx Figure 14.8.
Jp(X -t1x)
I
e-7
•
In(x + t1x)
(b) Hole impact ionizations only
I
Ax~1
x+Ax
I
t--1;> I I
x-Ax
I
I I I I
X
Schematic diagrams for only (a) electron and (b) bole impact ionizations.
i,1
"
60,j
~ .
-, .'
-1,- .,. --. '"
PHOTODETECTOR S
or (14.4.2) Its solution is (14.4.3) if all == an(x) is not uniform, since the electric field Ei x) may not be uniform. The multiplication factor M n for the electrons is defined as (14.4.4) For a uniform an' we have ( 14.4.5) and (14.4 .6) Here the multiplication factor is finite since W is a finite width. A similar procedure for holes propagating in the -x direction, as shown in Fig. 14.8b, leads to ( 14.4.7) and its solu tion is ( 14.4.8) The hole multiplication ratio is defined as ( 14.4.9) For the special case in which f3 p is independent of the position x , we have ( 14.4.10) and (14.4.11)
" ',, " '"
' ~ .. ..
14.4
607
AVALANCHE PHOTOL-IODES
14.4.2
Both Electron and Hole Capable of Impact Ionization
Let us write the complete coupled equations when both electrons and holes cause impact ionizations in the presence of optical generation as well: d
- In(x) dx
=
a n ( x ) ln(x) + !3 p( x ) l p( x ) + qG(x)
=
an(x)ln(x) + f3 p( x ) l p( x ) + qG(x) (14.4.12b)
d
- dx1p(x)
(14.4.12a)
Note that each impact ionization process creates an electron-hole pair, as does the optical generation rate G(x) per unit volume. We see that the above two equations lead to
:'1
( 14.4.13) :i
or the total current density
( 14.4.14) which is independent of the position, as it should be since this is a onedimensional problem. Any current passing through a surface at x has to be the same at steady state. The two coupled first-order differential equations can be solved using one of the two variables, for example, I n ( x ) :
where 1 is independent of x and is determined later by the boundary conditions. Noting that the first-order differential equation .'
d
-y(x) + p(x)y(x) dx
=
Q(x)
( 14.4.16)
has a solution of the form
(14.4.17) we obtain by setting all initial conditions atx o = 0: 1ft dx'!3p(x')e-CP(X') + Qf6"'G(x')e-CP(X') dx'
e -cp(x)
+ I n(O)
(14.4.18)
6C
~
PHOTOD'C.TECTORS
where ( 14.4.19) We then match the boundary conditions at x = W. Suppose In(O) and Jp(W) are given; we then find lll( W) Using and
cp(W) - cp(x') = fW[an(xl/) - ,Bp(x")] dx" x'
(14.4.21) we find J immediately:
.
Therefore, we have
In(x) = Je
o
0
( 14.4.23) where I is given by 04.4.22). The hole current density is then i
I p ( x ) =1~Jn(x)
(14.4.24 )
Alternatively, we can start with 04.4.12b) using J p as the variable and find _ f(w dx'[a n ( x ' ) 1 I p( x) -
+
qG(x')]eJ~r[(t,,(X") -f3p(x")JdX"
+
Jp(W)
e).tla,,(X')-Pp(X'»)d X'
(14.4.25)
and obtain another expression for I using the boundary condition at x I p(O) = J - .In(O): .
I I =
n
(
0) + I
p
W) e -
=
0,
(
(
(14.4.26)
ll
Let 1.I,S consider three special cases with only electron injection at x = 0, or hole injection at x = W, or optical injection G (x) at a position x.
-. . ..
14.4
AVALANCHE PHOTODIODES
609
Case 1: Only Electron Injection at x = 0 (Jp(W),= 0 and G(x) electron multiplication ratio is obtained from (14.4.22): I
M
n
=
=
0). The
e~(W)
=
InC 0)
Jaw dx'l3p(x')efxft'[an(X")-f3p(X")]dX"
1 -
(14.4.27a)
An alternative form, if we start with I p ( x ) from the- beginning and find I following the above procedures, is
I
Mn
=
I
.i
1 =
n(O)
Jaw dx'al1(x')e-fJ'[an(X")-f3p(X")]dXlf
1 _
Case 2: Only Hole Injection at x = W (J/O) multiplication ratio is, using (14.4.26),
=
(14.4.27b)
0 and G(x) = 0). The hole ~
I
Mp
I
=
i'~
e -!peW)
p(W)
1 _
=
Jaw dx' an(x')e-fu'[an(X")-f3p(X")]dxIf
Ii 'I
(14.4.28a)
'.I II
which is also a dual form of (l4.4.27a). A dual form of 04.4.27b) is
I M p - I p ( W) - 1 For example, if we consider
=
Jaw dx'f3 p( x')efx'f[an(XIl)-f3p(X")]dx"
an = f3 p
lAx) Using I n(W)
1
=
j :1 it
(14.4.28b)
-!
= constant, and G( x ) = 0, we find
If3p x
+ I n(O)
( 14.4.29)
I - I p(W), we find
I n(O) + I p ( W)
1=-~----
1 -
( 14.4.30)
f3pW
The results of I n ( x ) and I p ( .r ) are plotted in Fig. 14.9.
Current densities In(O)
I n(O)
o
w
Figure 14.9. The electron and hole current densities, InCx) and jp(x), and the total current density I as a function of position x for a special case Q n = f3 p = constant and the only injections are determined by the values 1)0) and IpWl).
.'
PH0TODETECTORS
610
Case 3: Only Optical Injection G(x') = GoMx' - x) (If/(O) = 0, Jp(W) 0). We find that the total current density is
=
(14.4 .31) and the multiplication rate depends on the position of the optical injection x:
We can also check two special optical injection positions x = 0 and x = W. We find
M(x = 0) = M;
(14.4.33)
-"vfp
(14.4.34)
and
M(x
=
W) =
These are the same expressions as in (14.4.27a) and (l4.4.28b), as expected. By controlling the electron injection in the p region or the hole injection in the n region, the multiplication factors Mn(V) and M/V) as a function of the reverse biased voltage V can be determined [24-31]. They usually increase very slowly at a low .reverse bias and show an exponentially increasing behavior above a certain large bias voltage, as shown in Fig. 14.10. These reverse bias voltages can be of the order of 30 or 40 V. Once M; and M p are measured, an and {3p are supposed to be found from (14.4.27) and (14.4.28). If both an and {3p are independent of the position x, the integrations can be carried out analytically. We can express an and f3 p in terms of M; and M p : a
n
=
( 14.4.35)
(14.4.36)
Figure 4.10. Multiplication factors for the electron dud hole injections, M'; and M p , respectively, are plotted as a function of the reverse bias voltage.
Reverse bias voltage V
14.4 AVALANcHE PHOTOD10DES
611
From the above discussions, we see that in order to determine the impact ionization coefficients from the multiplication of photocurrerit, proper experimental conditions [24-26] have to be met: (1) .Mn(V) and M/V) for pure electron injection and pure hole injection, respectively, have to be measured in the same diode, but not in complementary p + nand n +p devices, (2) the primary injected photocurrent (without multiplication) must be determined accurately as a function of bias voltage, and (3) the electric field should .be slowly varying in space and uniform in the active region. The dependence of the electric field on the position and bias voltage must be accurately known. It is not easy to meet all of these conditions without approximations. Experimental data for Si [27], GaAs [24, 25, 28), InP [26, 29, 30], InGaAs, and InGaAsP have been reported, for example, GaAs [25] InP [26]
a
=
f3:
=
(1)
. -,
(2)
(3)
InP [30]
1.899 X 10 5e - (5.75x 105 / E)UI2 0 j ern) 2.215 X 10 5e -(6.57 x 105/E)1.75 0 j ern) 240 kY jcm < E < 380 kY /cm, N = 1.2 X 10 15 cm " :' an = 1.12 X 107e -3.JI XIO hiE (Ly crn) (3p = 4.76 X 106e -2.55 X106/E (Ly cm) 360 kY jcm < E < 560 kY jcm, N = 3.0 X 10 16 cm "? an = 2.93 X 10 6e-2.64XIO hiE (Ly cm) (3p = 1.62 X 106e-Z.lJXI06/E Ojcm) 530 kY jcm < E < 770 kY jcm, N = 1.2 X 10 17 cm ":' an = 2.32 X 105e-7.16X 10 II IE! (l y'cm) f3 p = 2.48 X 10 5 e -6.Z3 x 10 11/ £ 2 (l j ern) 6 an = 5.55 X 10 6e - 3.10x 10 IE OJ em) {3p = 1.98 X 106e-Z.Z9X106/E (Ly cm)
InGaAsP (E g = 0.92 eY) [30] an = 3.37 X 106 e-2.Z9 X10 6 /E (ljcm) f3 p = 2.94 X 106 e-2.40 Xl0 6/E Cljcm) Ino .53Ga0,47As [30]
an
=
f3 p
=
2.27 X 106e-1.l3 Xlo6/E (ljcm) 3.95 X 106 e - 1.45 x 10 6 I E (I j em)
where the electric field E is in V jcm in the above expressions. For strained In o.2Ga o.sAs and Ino.15Gao.63Alo.2zAs channels embedded in Al o.3Ga o.7As material, the an and f3 p values have been found to be higher in In o.2Ga o.8As channels and lower in the Ino.J5Gao.63Alo.22As channels compared with the unstrained GaAs channels using hole injection in a lateral p-i-n diode configuration [31]. For an rms optical power 04.1.35)
(14.4.37)
6]2
PI-I0TdDETECTOR'.;
where m is the microwave modulation depth in 04.1.34), and P OP 1 is the optical input power. The multiplied rms photocurrcnt response is .
p rms
_
q7J-- M
lp -
( 14.4.38)
hv
where M = M n for the electron multiplication and M m ultiplica tion.
=
M p for the hole
Excess Noise. Since the multiplication processes are random, an excess-noise factor can be defined for the multiplication factor M, which is treated as a random variable, (14.4.39) wh ere < >means ensemble average. It has been shown that these excess-noise factors [32, 33] can bewritten in terms of the ratio of the impact ionization coefficients an / f3 » :
<M > +
[1
Fp = ~(M > +
(1
Fn = f3
p
an
n
a
f3 p
P
::)[2- <~,» a, )(
f3 p
2 -
electron inj ection (14 .4.40a)
11
<M,,>
hole injection
(14.4.40b)
>,
Note that if no avalanche multiplications exist, (Mn (lvfp ) , Fn , and Fp .are all equal to unity. In Fig. 14.11, we plot F; vs. ( M n ) for various f3 n / a n = k ratios. We see the increase of the excess-noise factor F; with increasing f3p/an for electron injection. The physical reason for this is that , in the case 1000
u..o, ~
o ~
...ou
.-~~...............---y-~~.......--~
k or 11k =
. . . . . . ""7""""""
100
~
c,
~
(I)
'0
10
Z
Figure 14.11. Th e excess-n oi se fact o r F vs. th e m ultip lica tion facto r ( M) fo r different valu es of the rati o of the e lec tro n and ho le ionization coeffi cients. For ele ctron inje ction, k = /3p /a" and for hol e injection, an1/3" = 11k should be used in the ratio.
o 10
100
Multiplication Factor Mn or Mp
1000
14.4
AVALANCHE
PHOTODIODE~
613
of electron injection from the p + region in Fig. 14.7, the secondary electron-hole pairs also cause impact ionizations. The holes propagate in the opposite direction to that of the electrons. Therefore, if (3pla is increased, the backpropagating holes will create more impact ionization currents. The measured amplified current at the end electrodes will have more fluctuating signals since these secondary or higher-order impact ionization processes will contain more random characteristics. For hole injection, 1 If!, should be used in the same diagram . The multiplication or gain noise is given by ll
(14.4.41) The mean-squared shot-noise current after multiplication is generalized from the shot noise in (14.1.49) by adding the factor (M 2 ) «~) = 2q( t; =
+ Is + I D)<M 2 ) B 2q( I p + Is + ID)(MiFB
( 14.4'.42)
where I p is the average steady-state photocurrent (l4.1.34b), IBIS the background current, I D is the dark current [34-36], and B = tif IS the bandwidth. The thermal noise is (ij) -
(14.4.43)
where 1 I R e q = 1 I R j + 1 I R L + 1I R j , accounting for the junction resistance R j' the external load resistance R L and the input resistance R j of the following amplifier of the photodiode. For the modulation depth m = 1, the signal-to-noise ratio (power) for the avalanche diode is [8, 21]
N
t( q'YJPopt I
·2
S
lp
(i~)
+
(i})
hV)2 <M)2
2q( i, + Is + ID)(M/FB + 4k B TB I R e q
( 14.4.44)
Since F(M) > 1 and is a monotonically increasing function of the average multiplication ratio <M), the above signal-to-noise ratio can be optimized at a particular value of <M) . High-speed detections using avalanche photodiodes and their time dependence or frequency response have been investigated [37-40J. For M o > ani f3 p » the frequency-dependent multiplication factor is
Mo
M(w) - - - - - - 2] 1/ 2 [ 1 + (MOWT t )
( 14.4.45)
where T t is an effective transit time through the avalanche region. The effects of the avalanche buildup time have also been reported [39].
. .. .
I " "
("
,.r' .. .,.,
j,. .. .,...
~~
~ ,
,
_~.
"
' '," .,
- ,,.. .....
~~
-." -
- ~,..
I" ·
.. •.•
.• •
PHOTO DETECT':)R:>
614
Separate Absorption and Multiplication (SAM) APD [29, 30, 41, 42]. Various contributions to the dark current of an APD have been investigated , which include the generation-recombination via midgap traps in the depletion region, tunneling of the carriers across the band gap and a surface leakage current across the p-n junction in InGaAs APD, for example. When the reverse bias is above a certain value before the breakdown voltage VB' it has been found that the tunneling current is dominant, unless the doping density N D in the absorption region can be reduced below a certain value in which the tunneling current can be reduced to be smaller than the generation-recombination current. A separate absorption and multiplication structure has also been proposed (41] to reduce the tunneling current. The geometry is shown in Fig. 14.12a, where a low-field InGaAs region is used as
(a) SAM APD
Multiplication region
n-InP
Absorption re ion n·lnGaAs
V
p(z)
z -qN 0 2 -qN 0 1
(c) Electric field profile E
'--
= i. E(z)
-qN 0 3
E(z) I-----.-~-----..-+----------+__l......---~z
~
Small bias Large bias
Figure 14.12. (a) A schematic d iagram for a separate absorption and multiplication avalanche photodiode (SAM APD), where the absorption occurs at the narrow bandgap InGaAs region and the photogene rated carriers are swept into the InP multi plica t.ion region where the electric field is larger. (b) Charge density profile pC z ) under a large reverse bias. (c) The electric field profile (solid lines) under a large reverse bias. Dashed lines show the electric field profile for a small bias voltage.
•.
~
."
.~
.
14.4 AVALANU-IE PHOTODIODES
615
the absorption region and the photogenerated carriers are swept into the high-field InP binary region where avalanche multiplications occur [16]. Since the InP layer has a larger band gap than that of the InGaAs absorption region, the tunneling current can be reduced. The electric field profile E(z) = iE(z) can be obtained using the charge density profile p(z) based on the depletion approximation at a large reverse bias voltage since JsE(z) /Jz = p(z). Since 6 is slightly different in InGaAs and InP layers, a slight discontinuity in Ei.z ) occurs at the InGaAs/InP interface. Multiple-Quantum-Well APD. Heterostructure avalanche photodiodes have been fabricated for high-speed low dark current operations [41-43] since the late 1970s. Research on quantum-well photodiodes was started in the early 1980s. A plot of the excess factor F shows that the excess noise factor is minimized if f3 p / an « 1 using electron injection or an / f3 p « 1 for hole injection. In those limits, an ideal single-carrier-type multiplication process will dominate, and the excess noise caused by the feedback process of the impact ionization caused by the secondary electrons or holes in the opposite direction can be minimized. Ideas using multiple-quantum-well (MQW) structures for APD applications have been proposed and explored both theoretically and experimentally [44-52]. For example, consider GaAs / AlxGal_xAs MQW structures as the impact ionization region for electron injection (Fig. 14.13). Since s e.r s «, = 2:1 s, = 0.67 fl£g' fl E; = 0.33 fl £g), the electrons coming from the left barrier region will gain a larger kinetic energy fl E; when entering the barrier region than that of the holes traveling in the opposite direction. Therefore, the electron impact ionization coefficient an will be enhanced compared with f3 p • We expect a n / f3 p » 1. The excess noise factor is expected to be minimized. Measurements of the effective ionization coefficients an and f3 p show an enhancement of a n / f3 p from 2 in a bulk GaAs to about 8 in a GaAs/AlxGa1_xAs
cs
p
N
Figure 14.13. A multiple-Quantum-well avalanche photodiode using' GaAs/AlxGa1_xAs with the property that the ratio of the impact ionization coefficients an /f3p is much larger than one since t1 E; is larger than t1 E,..
I
I.
I' I
i
II .
'I
616
PHOTODFI'ECiORS
multiple-Quantum-well structure [45, 46] and M n , = 10 at an electric field E = 250 kY/cm. It has also been reported [47] that this ratio cx n / f3 p varies (not monotonically) with the aluminum mole fraction x. At higher values of x (~ 0.45) above the onset of indirect electron transitions, the noise is increased. Intersubband Avalanche Photomultiplier. Avalanche photomultipliers using an intersubband type (bound-to-continuum state transition) in an n-type doped or p-type doped multiple-quantum-well structure have also been proposed and investigated both theoretically [50, 51] and experimentally [52-54]. The idea is to introduce electrons in the quantum-well regions by doping the wells n type. Incident photogenerated carriers will "impact ionize" those carriers confined in the wells and kick them out of the wells via Coulomb interaction contributing to the avalanche multiplication current. Since this is a single-carrier type of photomultiplication, the excess noise is expected to be minimized. Experimental results on this intersubband avalanche multiplication have been reported [52-54] .
14.5
INTERSUBBAND QUANTUM-WELL PHOTODETECTORS
In Section 9.6, we discussed intersubband absorption in a quantum-well structure. To provide carriers for the intersubband transitions, donors for n-type electronic transitions have to be introduced in the quantum wells (or barriers) to provide free electrons which will be confined in the well regions at steady state without a bias voltage. When an incident infrared radiation illuminates the QW detector, electrons may absorb the photon energy and jump to a higher energy subband and be collected by the electrodes with an applied voltage. Theory and experiments on intersubband absorption and quantum-well intersubband photodetectors (QWIP) [55..:.87] have been investigated for long wavelength applications, which may be competitive with HgCdTe detectors. The advantages include the mature GaAs growth and processing technologies for high uniformity and reproducibility. For an extensive review of the subject, see Refs. 86 and 87 and the references therein. For n-type multiple quantum-well photodetectors, the optical matrix selection rule shows that the optical polarization must have a component along the growth (z ) axis, i.e., it must be TM polarized, as discussed in Section 9.6. For TE polarized light, the absorption is expected to be very small. However, . for p-type doped quantum-well photodiodes, the valence-band mixing effects due to the heavy-hole and light-hole states show that the x- and y-polarized light can have as large an absorption coefficient as the z-polarized light [87-90]. Therefore a normal incidence geometry is possible for p-type QWIP. In this section, we discuss mostly n-type QWIPs because of their potential for 3 to ~-,um and 8 to 12-,um photodetector applications. In Fig. 14.14, we
14.5
INTi:RSUBBAND QUANTUM-WELL PHOTODETECTORS
(a) 45°-Edge-coupled QWIP
617
(b) Grating-coupled QWIP
V
Multiple quantum-well k'"" absorption
y,
region
~11~~~~~b ~
~
j---±---t---~---I
Incident radiation '------tF-------l
hv
n" contact
AlAs reflector Thick GaAs substrate
Incident radiation Figure 14.14. Schematic diagrams of (a) a 45°-edge-coupled quantum-well infrared photodetector (QWIP) and (b) a two-dimensional grating-coupled QWIP.
show two examples using (a) a-4SO-coupled QWIP and (b) a two-dimensional grating-coupled QWIP. These designs provide the necessary polarization selection rule such that the infrared radiation will have a component along the growth direction of the multiple quantum-well absorption region. Our theory in Section 9.6 shows that the absorption spectrum is a Lorentzian function: a(hw)
r/(27T) =
ao
(E 2 1
-
hw)
2
+ (r/2)
2
(14.5.1)
where the intersubband energy E 2 l = £2 - E 1 is the subband spacing in a simple single-particle model as presented in Section 9.6. If the Coulomb interactions and screening effects are included, E 21 will have a slight shift due to the many-body effects [91-94]. The measured absorption spectrum [87] for a bound-to-bound transition is shown in Fig. 14.15 as a Lorentzian 2 shape. Note that the absorption is dependent on 1<1 ; therefore, a rotation of the polarization as a function of the polarization angle
PHOTODE rL CTOR.~
618
1.4r-------~----------------_,
1.2 1.0
WAVEGUIDE
w 0.8 u z
CD
~ 0.6 (f)
CD
0.2
oL-------2000
1800
1600
1400
PHOTON ENERGY
1200 11
1000
800
(em-I)
Figure 14.15. Measured QWIP abs orption spectrum for a multipass waveguide geometry. (Afte r R ef. 87.)
oscillator strength (i.e ., the intersubband dipole moment) and the escape probability can be optimized. For a bound-to-continuum state transition (Fig. 14.17b), the electrons have a greater probability to transport into the barrier region and be collected by the electrode and contribute to the photocurrent, although the intkrsubband dipole matrix between the ground state £1 wave function and the highly oscill atory continuum-state wave function may be smaller. For a simplified ana lysis [87 , 97, 98], we look at Fig. 14.17b, where P c is treated as an effective capture probability for an incident current I p for both the case (a) bound-tobound and the ca~e (b) bound-to-continuum transitions. Vie obtain Pc I p as th e fraction of incident current captured by the well and (l - P c)Ip as th e remaining curre nt transmitted to the next period. The incident infrared radiation cre ates a photocurrent i p: (1 4.5. 2) wh ere
l4.5
INTERSUBBAND QUANTUM WELL PHUTODETECTORS I .O@---~----------
6~9
---.
0 .6
I
0 .6
8-73-
.q:
e N
~
~
0 .4
0 .2
O'----'--......L---'---l---L-_--l..._-4I~--=~~.
30 40 50 60 POLARIZER ANGLE ¢ (DEG)
90
Figure 14.16. Experimental results for the polarization selection rule showing the peak absorption YS, the polarization angle eP where eP = 0° is TM polarization and eP = 90° is TE polarization, all at an angle of incidence Os = 73°, the Brewster angle. (After Ref. 95.)
(a) Thermionic emission (b) I p -+_-f::::::j~A.C:~Tunneling ~
.-
+-L~
Figure 14.17. (a) Bound-to-bound state transition and (b) bound-to-continuum state transition in a biased quantum-well infrared photodetector. The well width L w in (b) is designed to be small enough such that only one bound state exists in the quantum well and the second level £2 is pushed into the continuum.
~~'§,
_..
- -- "_ . . - ----" .
-
620
PHOTODETECTORS
From current continuity, we have
(14.5.3) Therefore,
(14.5.4) The total net photocurrent is (14.5.5) where g is defined to be the overall photoconductive gain, and 7J is the overall quantum efficiency of the MQW photo detector consisting of N w quantum wells. We have 7J ~ Nw7Jw if 7J « 1 since 7J is proportional to the absorbance of the structure . From 04.5.2) to (14.5 .5), we find
g= -
1 7Jw
- -=
1
(14.5.6)
Pc 7J
which gives the value for gain . The capture probability Pc decrease almost exponentially with the applied voltage [87].
IS
found to
Dark Current [87, .99, 100]. A simple model for the bias-dependent dark current I D is to take the " effective" number of electrons n*(V), which tunnel out of the well or are thermally excited out of the well into the continuum states, multiplied by the average transport velocity v( V), the cross-sectional area of the detector A and the electron charge q:
(14.5.7) where m*
n*( V )
,e
7Tfz-L p
f ( E)
f
I [
00
f(E)T(£ ,V)dE
(14.5.8)
£1
1
-
.-I
--=-----:::-:-~
(14.5.9),
where E F is the Fermi level measured from the conduction band edge (same as the first subband level £1)' and L p is the length of a period. T(E, V) is the tunneling probability through the triangular barrier with a bias voltage V. The velocity is
(14.5.10)
I
14. 5
I
Nt cRSUB
.
. .
BAN
D QU ANTUM-WELL PHOTODETECTORS
62 1
10-~
---
-..... <:{
10- 6
-
"U
~-
:2: lu
0:: 0::
10- 8
~
u
~
0::
<:{ C)
1 2 3 4 5 Figure 14.18 BIAS VOLTAGE, Vb(V) functi on . bark CUr re of the bias 1 n ts from me asured (solid curves) and calculated (dashed) data as a 107 . /-trn . (A.fte r Ref. 9v9~)tage a t various temperatures for a QWIP with a cutoff wavel ength
Where . /J.. IS the 1 bi la s Volta ge V and e ectron mobTt Vel' I 1 y, F is the average field determined , by the . OCity. the overall MQW width and u is the saturation drift The abo v . s ' a ve e slrnplifi d .h ry gOod ag e model has been used to explain the dark current WIt even mOre sin-. rel~firnent, as .up 1 ed d shown in Fig . 14 . 18 for a 10.7 p..m QWIP (99). An rno el [loa, 101] assumes that
T( E ) where E . II I B IS the ban i vv e obtain
er
hei
~ {~
( 14. 5 .11)
.
eIght on the right-hand sid e of the qu antum well.
(14.5.12)
where E
c :::: E B
-
E . 1 is the Spectral cutoff energy. The dark current becomes
(14 .5.13)
620
Pi-JOTODETECTORS
From
r
is determined from
(14.5.14) plotting In(JDIT) vs. (E e - E F ) should give a the result of E e - E F can also be compared with the optically measurea spectral cutoff energy Ec- This simple model has been reported to agree with experimental observations [87, 99, 102]. F)k 8 T ,
PROBLEMS 14.1
Consider a photoconductor (Fig. 14.0 that is an extrinsic semiconductor bar with a thickness d = 0.1 mm, a width w = 1 mm, a length t = 4 mm, and an acceptor doping concentration 10 15 em -3. Assume that the electron mobility f..L n = 3000 em" V-I S-1 (» J.L) and the applied voltage V -= 4 V. (a) If the photoconductor is illuminated by a uniform steady light such that the optical generation rate of electrons is G n , find an expression for the photocurrent 1p h = 1 - 10 , where 10 is the dark current, and 1 is the current when there is illumination of light. Find a numerical value for 1p h if G n = 10 16 em -3 s -) and 3 Tn = 10 s. (b) If the photoconductor is illuminated by a uniform light with a sinusoidal time variation, that is, GnU) = g cos co t, show that the photocurren t is given by the form
What are I p and ¢ in terms of g and Tn' etc.? What determines the 3-dB cutoff frequency in the frequency response of the photocurrent? (c) If the light has a dc (steady) and an ac component as may be used in optical communication, Gn(t) = GoO + m cos wt), where the constant m is usually caned the modulation index, find an expression for the photocurrent using the results from parts (a) and (b).
IT,
14.2
Expla in why the photoconductive gain than 1.
14.3
Derive 04.1.34a) and (l4.1.34b).
14.4
Derive the junction capacitance C, for a heterojunction using the depletion approximation in Section 2.5 for a p-N junction.
Tn
can be much larger
PROBLEMS
623
14.5
Derive the RoA product in 04.2.15).
14.6
Replot Figs. 14.6a-e for a p t-n "-n + photodiode, where a plus superscript means heavy doping concentration and a minus superscript means light doping concentration.
14.7
Derive (14.4.26) and (14.4.27a).
14:8
An avalanche photodiode with the electron and hole ionization coefficients an and {3 p is assumed to have a uniform field in the impact ionization region such that an and f3 p are independent of the position x. The electron and hole injections are given by In(O) and I/W), and the generation rate due to optical injection is G(x). (a) Write the two equations for the electron and hole current densities and solve for the hole current density as a function of x in terms of the injection conditions In(O) and I/W). Find the total current density I. (b) We assume that the electric field in the avalanche region is . - ... uniform such that an and (3p are independent of the position x. (i) If G(x) = 0 for all x, and In(O) = 0, find the multiplication factor for holes, M p , defined by
(ii) On the other hand, if G(x) = 0 for all x, I/W) multiplication factor for electrons
1M \
(c) Using the results in (b) for
n
=
0, find the
I =--
InCO)
M; and M p show that an and {3p can
be determined from (14.4.35) and (14.4.36) once M n and M p are measured:
!
14.9
an
=
(3p
=
Discuss the physics for the excess noise factor F( M) How can this excess noise be minimized?
=
<M 2) /
(M)2. !i
u
ir \!
I~ ~
;,
674
Pi ;OTODETECTORS
14.10
Derive 04.5.12) and (14.5.13).
14.11
Discuss the polarization selection rule for an n-type doped quantumwell infrared detector using intersubband transitions. Why are the configurations such as a 45°-edge-collpled structure or a grating-coupled structure used in the designs of these intersubband photodetectors?
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62~
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i:
.,I
626
PHDTODETECTORS
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628
PHOTODETECTORS
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Appendix A The Hydrogen Atom (3D and 2D Exciton . Bound and Continuum States) [1-5] A.I
THREE-DIMENSIONAL (3D) CASE
The hydrogen atom is a two-particle system described by
H
=
-
tz2 --V2 2m 1 I
-
tz2 - - V 2 + VCr - r ) 2m 2 1 2
(A.I)
2
A general method to solve this problem is to change the variables to the center-of-mass coordinates R and the difference coordinates r:
.;
J J
I
.,
(A.2) (A.3) We define the total mass M
(AA) and the reduced mass m ; 111
-=-+m,
ml
m2
(A.S)
The first two operators in H can be rewritten as
(A.6)
where VR and Vr are the gradients with respect to Rand r. Equation (A.6) 631
THE
I-fYC:;:~ OGEJ~
A1\)M (:;D AND 2D EXCITON STATES)
can be derived using the fact that
a ax a ax a m1 a a -=-- + --=--+ax! aX l ax aX l ax M ax ax a ax a ax a m2 a a -= --+--=---aX 2 aX 2 ax aX 2 ax M ax ax
etc .
We can show the relation in (A.6) for all terms involving a2/ax~, a2/axi, a2/ iJ X 2 and a2/ ax 2 , then use an analogy for other components. The original Schrodinger equation
(A.7) can be separated into two parts if we let
where
(A.8) (A.9) and the total energy E T is
(A.I0) The eigenenergy and eigenfunction of the first equation (A.8) in the centerof-mass coordinates are simply those of a free "particle" with a mass M: EK
1i 2 K =
-
2
(A.ll)
-
2M
and eiK
f(R) =
·R
(A.12)
IV
Once !/J(r) is solved from (A.9), the complete solution is given by
e iK rJ; ( r 1> r J =
'R
Vv
Iff (r)
(A.13)
A.I
THREE-DIMENSIONAL (JD) CASE
6,~3
Solutions of \fler) for the Coulomb Potential
Using the definition of Vr 2
(A.14) the solution to Equation eA.9) with the Coulomb potential V ( r)
=
-
e2 -4-rr-c-r
(A.15)
can be obtained by the separation of variables:
ljJ(r) " "
=
R(r)e(e)ep(~) = R(r)Y(e,~)
(A.16)
and d2
--ep + m 2 ep
=
0
(A.17)
m 0 + A0 sin' e
=
0
(A.IS)
+ rVer) - E]R(r)
=
0
(A.19)
d~2
1 d ( ~- -- sin sin e de
11 2
1 d2
- - - - e r2R ) + Zm , r dr
de e-
de
11 2 A --R Zm , r 2
1-
2
Spherical Harmonics Solutions yfmeO, '1')
It is easy to see that the solution for
1
.
= - - e 1m cp
(A.20)
J2rr
where m is an integer, since
~
with a period 2rr.
g = cos e, leads to
(A.21) One notes that the above equation is even in g, that is, if g ---) - g, or equivalently, e ---) -tr - e, the same equation is obtained. Thus the solution is symmetric or antisymmetric with respect to the x-y plane.
'~Hi:
(j34
LYDROCJE;,r ATOi;
em A'..m 2D EXCJTON STATES)
If m = 0, the above equation becomes
-d [ (1 - t 2 )
dg
dP]
-
dg
+ AP = 0
(A.22)
which can be easily solved using the series expansion: co
(A .23)
A recursive formula is then obtained by substituting CA.23) into CA.22): k(k+l)-A
(A.24)
(k+l)(k+2)a k .
--
If the series does not terminate at some finite value of k,ak+2Iak ~ kl + 2), and the series will not converge at PCg = 1). Thus A must be an integer A = t Ct + 1) for some finite value t, that is, k = t, where t is an integer. The solution is
(k
P (C) _ f
S
-
1
[t /2] ~
( -
1) k (2
t-
2k ) !
~f-2k 2 t k'-::O (t-k)!k!(t-2k)r s
(A.25)
where [ t 12] means the largest in teger < t 12. Ip general, the solution to CA.2l) is given by the associated Legendre functions satisfying
where
1 - 2ft!
__
_~
(1
-
2) m /2
e
dt+m
de f + (2 e - 1) r m
(A.27) for positive m .::;
t.
For negative m with
1m!
~
t, 1m! should be used in
CA.27)
A.l
us
THREE-DIMENSIONAL (3D) CASE
since the differential equation (A.26) should give the ' same results for The first few polynomials are
t=o,
Pg(t)=l
t= 1,
P10(t)
=
t
pl(t)
=
11 - t 2
t=2,
+ m.
pf(t)=~(3t2-1)
Pi(t)
=
3tl1 - t
p}(t)
=
3(1 - t
2
2
(A.28)
)
.!
Noting that
;.
:. .'
f with 0 <- m < c,' -taine d :
t,
[PF(t)]2dt=
l
2t
-1
(t+m)! + 1 (t - m)!
2
the normalized solutions for the angular dependence can be
2t
"+
1
(t - Iml)! ( t + Iml)!
- - - ---~- (_1)(m+lml) /2 p).ml(cos
4'1T
and
(A.29)
e) e i m tp (A.30)
"
f
2 7r
(7T
J,
2
IYf ( e, cp) I sin ede d cp
=
1
(A.31)
cb =O 8=0
The first few spherical harmonics are
t
=
0
(s orbit)
Yoo
1 =--
J4rr
(A.32a)
r·
636
THE
1= 1
;r ( I ) i ~O G E N
}\ T O M OL AND 1 D EXCITON STf'. TES)
(p orbits)
{;3 Of; -
477
Y , ±lO,'P) =
cos f3 =
{;3
Z
_ . - == 4'77" r
3 5in Oe± ;. 8",
~
Of;
IZ) 3 x ± iy 8", r
1
- + - jX±iY )
(A .32b )
,fi
1= 2
(d orbits)
Y , oCO,'P)
~ ; 16rr 5
Y z ± 1( (3, 'P) = + Y
((3 Z± 2
m) ' T'
=
/
~; 16rr 5 [3Z r
2
(3C05 'O - 1)
{!ls -
-8 sin f3 cos '"
(3 e
::!:
15 . - sin? (3 e ± 2 1"., = 32",
-
2
.
1'1'
=
fi'S
+ -
{ff
1)
-
(x + iy ) z
-2
8",
. -,-
r
15 (x + iy Z ) 32", rZ
-
(A.32c)
Radial Functions for the Bound and Continuum States The r adial function Rt r ) satisfies Il Z
h2
1 d2
- ---z(rR) + Zm , r dr
t (t +
Zm , ;
.'
r
2
1)
R + [VCr) - E]R = 0 ( A.33)
\,
which may be rewritten in the form r
d Z _ t( I+1 ) Zm , 'I { _ + ~ z [ E - V( r )] f~u (r) z
dr
r
2
rt
=
0
(A.34)
where
u(r ) = rR(r)
(A .35)
Let us define the Bohr radius
(A.36)
A.I
THREE-DIMENSIOl'{AL (3D) CASE
and 1
ko
=
The Rydberg energy R y is defined as
(A.37)
In the following, we consider the bound and continuum states. Case 1: 3D Bound State Solutions (E < 0). For bound states, we define the variables
(A.38) 2r
p=v«;
(A.39)
Equation (A.34) reduces to
(AAO)
If we look at the asymptotic behavior of the function u(p) at p ~ co from (AAO), we find (d 2/d p 2 - t)u(p) = 0 and the solution should behave as exp( p /2) or exp( - p /2). The latter term exp( - p /2) should be chosen, since the former blows up as p approaches infinity. If we look at p ~ 0, the differential equation (AAO) is
d 2
[
.
-d 2 p
t( t + p2
1)] u(p)=O
.'
(AAl)
for t =/= 0, and its solution is either p t+ 1 or p -to The former should be chose~ since ui p) should be a regular function at the origin. Thus, in general, we .may assume u( o) of the form u( p) = e -p /2 p i' + l/( p)
.'
(AA2)
!
'~
~ -.
'- '
.,... \ ...... .'"t , -I' . ,; ,• •• •..,......... "' ••••
THE HYDE.O (;[:
638
,~
_~ ,, --
~ . _ .
}\T O M U P AND
_ .
~
...
~
.~ D
•• •• .
~
. . .... . ~ •. ~ - . ,- -' _ .
- ~
"
. ,
EXCITON STATE.S)
Equation (A.40) reduces to
d 2f ( p ) df(p) P .d 2 +(2t+2-p) dp +(y-t-1)f(p)=O p
(A.43)
By checking a series solution to the above equation, it is found that (y 1) must be an integer N, N = 0,1 ,2, .... Or
=N+t+ 1
y
t-
(A.44)
=1l
Using n as the principal quantum number, we have
t=
0, 1,2, ... ,n - 1
(A.45)
The solutions of the differential equation of the form d2
df
p - f + ({3 - p)- - af= d p2 dp
°
(A.46)
are the confluent hypergeometric functions,
F(a,f3 ;p)
=
a p a( a + 1) p2 a( a + 1) (a + 2) p3 1 + f31! + f3(f3 + 1) 2! + (3({3 + 1)(f3 + 2) 3T + (A.47)
Note that Ft;a, f3 ; 0) = l. We can identify that solution for ui p}:
a =
-
n
+ t + 1 and f3
=
2t
+ 2 and obtain the (A.48)
We can check from the definition in (A.47) that the polynomial F in (A.48) terminates after a finite number of terms since t < n - 1. Alternatively, the associated Laguerre polynomials L';:(p) are used. It is related to F by m
L';:(p) =( -1)
(n !)2
I( _ ),F(-(n-m),m+ l;ZY ' m. n m.
(A.49) Note that Lr;:(O) = (_l)m(n!) 2/[m!(n - m)!]. Therefore, ui r ) can also be
A.I
THREE-DIMENSIONAL (3D) CASE 63~
written in the form
(A.50) where C is a constant to be determined by th e normalization Condition . Using the in tegral identity
lo
co
e
-p
P
2!+2{L 2f'+ I ( p ) J 2 d n+f'
2n[(n +1)1)3 (n -1-1)!
p= ~
(A.51)
or
f
jOOe - p U +2[F ( _ n +f+ 1,21'+ 2;p)]2 dp = p
.1
2n[(2f+ 1)!]2(n '-f-l)'
(n+I)!
o
f
I
.
f I
(A.52) we find that the radial wave function satisfying the nor . . mallzatlOn Condition
I
f I' f
J
l°OR2(r)r2dr = 1 o
i
(A.53)
IS
R
n ,
3/2(
2 ) ( ( r) = na o
(n - 1 - 1)! ) 2n[(n
+ f)
11'
)3/2[
(2/na o (2/+1)!
--
x
(n + 1 )! 2n(n-I-1)!
1/2
}l/2
I'
e-
' / ( OOO
)(!f:) L~~i' (!f:)
. 0;;;;;
e-r/na (
t
2r)
F(- + 1+ 1+ 2;~) 1, 2
n
nao
As r ~ 0, Rn !(r) ~ (2r /ncz.o)t,. which is nonzero only when The complete wave Iunctions are 1 = O.
.
_
1
\1;;
.'
(A.55)
The first few wave functions are .1, _ 'f/ 100 -
.'
(A.54)
(1)3/2 _
ao
e -r/a o " __ •
. ( 15 state). I
I.
i
! ;
{ i
-. ...-
1i~~'-~.
.._....-~._.- ....... '\._ ._ .. -' .... __..,.,.,.
. .. ',. . - "':.-0
riu.
,
~_
•.-
~-
·
C_..'f'7"'~_·.~.· _
"~-:'~~ ' ''1"' .- " ., :-r-; "
-"f" '. ,. '
._
LYI)[tJI,_',!::: .J ATOM (}D /\N9:D EXCITON
,..,
..
STATES)
(2s state)
.f, 'PZ1O
r/J21 ± 1
1
= 2v~ 27T
(J -
«:
r
= O,l/J
=/:-
r
--
)
e- r /
Z lI o
cos (]
(2p state)
z»;
1 (1 )3/Z(
= - - -4[;; «;
Note that at
)3/2(
r)
,
- - e -r/Za o sin (] e ±
z«,
t
0 only if
= m =,
iii'
(2p states)
(A.56)
0 (s states). We have
2 (
na o ) 3/
2
and
(A.57)
The wave function at r = 0 will be useful when we study the exciton effects on opt ical absorption in Chapter 13. Case 2: 3D Continuum-State Solutions (E > 0). When the energy is posi, tive, the solutions will not be quantized. Instead they become continuous. The solution to (A.34) for the radial wave function is -obtained following the change of variables as in (A.38) and (A.39),
yZ
,
=
(A.58)
2r p = - - = 2iKr vI a 0
We choose Ill' = ix, where number, since
K =
..jEIR y
E=
2m,
-
(A.59)
=klk o is the normalized wave
(A.60)
A.l
THREE-DIMENSIONAL OD) Cf\SE
641
and the Rydberg is
Ry =
(A.61)
and !: = r / a 0 is the normalized radial distance. The solution u(p) has the same form as in (A.48),
(A.62) We therefore look for the normalized radial wave function of the form -.
RKtC~) = N, ( 2Kr) e exp( - iK~) F( f
+1+
K
~, 2 f
+ 2; 2i«[J (A .63)
such that (A.64) in the ~ space. Later on, we change the normalized variable ~ to the real spacelistance r, and the 8(K - K') normalization rule to the 8(E - E') normalization rule. We note the asymptotic behavior of F,
(A.65)
as [z ]
~
00 ,
We thus have
_
f
- N K f ( 2 K r ) (2 t .
-
,
+ 1). [
exp ( 1. K !: )
(,..,.
d K~
r(G + iJ
1
) -t-l + i
+
,\
11K
)
/
/K
+
c.c.]
(A.66)
T H E rr ( i) R OG E f-.J' }\T !)1vi (3D AN D 2]) EXCITON STATES)
fA 2
where c.c. means complex conjugate of the first term in the large bracket. We use Tt z ") = [T(z I]", 2iK[ = exp]i 71"/2 + InC2K[)],' and
(2 'LKT- ) - t - ,l+i /K
=
(2'IKT ) - t-1(2 lKT ' ) i/ -
K
~
The radial function can be written as for
e-
(2 t'+1)! bKt=NKt
7T
00
(A.68a)
/ (2 K )
If(t'+l+i/K)1
K
T -')
(A .68b)
and the phase factor is
(A.68c) The normalization condition is d etermined by the asymptotic behavior of R Kt as!. -') :t:'. Since K [ » Cl/K)ln(2K[) and 0K '( , we find
(A.69 )
Therefore, we choose bK ( = V2/7T to .satisfy the O(K - K') normalization rule (A.64). In deriving (A.69) , we have expressed COS(KT) as the sum of two exponentials and use !
(A.70) noting that
K, K'
are both positive..' F rom b
_ f2 N r - V-;; K
K
K {
,
we find
+ 1 + i/K)I (2 t' + I)! ,
e'TT/ (2K )lf( t'
(A.?! )
A.,
THREE-DIMENSIONAL (3D) CASE
643
and RKrC!.) is given by (A.66). The quantity [I'( ated noting that for
t
t+1+
i/K)1 can be evalu-
= 0,
(A.72) For t> O,fC(+ 1 + ilK) ilK), and
~)
r(t+l+
=
2
Ct+ i/K)(t- 1 + ilK) ... (l + i/K)fO +
~)r(t+l- ~]
=r(t+l+ =
[n (S2 + ~)] 5 =
1
K
2
TrIK
sinh( tr I
(A.73) K)
Therefore, we obtain
»:
=
['2:
V;
Ke /(2K) [n" (S2 + 1T
(2t+1)! 5=1
K_ ]
I _1 )] 1/2[_.7r_ K
2
1/2
smh(7rIK)
(A.74)
If we change the normalization rule to the physical quantities in terms of R E f(r) . '1 the real space r and use the energy normalization rule,
(A.75) we obtain _i_, 2 ka o
t+
2; 2ikr)
(A.76)
(A.77) Again, as r ~ 0,
J!.EeCr)
~ C2kr)!, which vanishes except for
t
=
O.The
!'HL
644
}-!YDPOGE~' ATC,l':l
(38 AND 2D EXCITON STATES)
complete wave function is given by
(A.78) where the spherical harmonics Yt m(e, 4» are given in (A.30). At r = 0, we find !/JEtm(r) =1= 0 only if t = m = O. Therefore, using CEO = [e 1T / K j sin h( 7T j K)JI/2 and Y oo = Ij,J4'IT, we obtain 1T
K
1 [ e 1 I!/FEoo(r = 0)1 = - ya R 3 . h( / K ) -4 SIn 'IT 'IT o 2
A.2
/
]
(A.79)
TWO-DIMENSIONAL (2D) CASE
In this case, the position vectors of the two particles r l , r 2 , the center-of-mass coordinates R aJ;1~L the difference vector r are all in the x-y plane. All the expressions still follow the equations (A.l)-(A.ll), except that only the .r-y dependence exists, i.e.,
VCr) = where r = xX + YY =
(A.80)
47TSf
x 2 ) i + (YI - Y2)Y' The solution is
(Xl -
e iK · R
!/F(r 1 , r 2 ) = -
a
!/F(r)
(A.8l)
where A is the cross-section area, and !/F(r) satisfies
(A.82)
The solution is of the form
(A.83) and the radial function satisfies 1 d d -; dr r dr [
m
7
2
2m r
+
~
l (
2
) 1 e E + 4;';; R( f) = 0
(A.84)
A.2
TWO-DIMENSIONAL (2D) CASE
Case 1: 2D Bound State Solutions (E < 0). Using a change of variables, the same as those in the three-dimensional case (A.38) and (A.39),
Ry
-E
(A.85)
2r p=
(A.86)
we obtain d2 ( d p2
+
1 d
-~
P dp
m
2
- -
p2
1]
Y P
+ - - - R(p)
=
4
0
(A.87)
As p --) 00, we find the dominant terms above are (d 2jd p2 - i)R(p) Therefore, we set Ri.o) = e- p / 2h ( p ), where h(p) satisfies . 2
d [ d p2
+
=
O.
-......
(1- p) d P dp
1( Y p
1 2
+ -
m2 p
-
-
) ]
h(p)
=
0
(A.88)
As p --) 0, we find that the dominant terms are 2
1 d m d2 + - - ( dp2 P dp p2
Therefore, R(p) behaves like find that f( p ) sa tisfies 2
• [ P-2 d + dp
p1m l.
)
h(p) = 0
(A.89)
We then assume that h(p)
=
d + ( Y - -1 - Iml J] f(p) (2Im/ + 1 - p)-
dp
2
p,m1f(p), and
=
.
0 (A.90)
If we compare the above with the definition of the confluence hypergeornetric function Fi cc, {3; p ) in (A.46) and (A.47)
d2 . d ] P d 2 + ({3 - p) dp - ex F(~,{3;p) [ p
=
0
(A.91)
we obtain
f ( p)
=
F ( Im I +
t -- y, 21 m I + 1; p )
(A.92)
The above polynomial should not approach infinity faster than any finite power of polynomials, and the acceptable solution is only when jml + -i - Y
Tli F I-!'(DRO ::JEl': ATOM
646
( 3~)
AND 20 EXCTON STATES)
t
:L n
is a negative integer, i.e. , y ~ Iml + or use 'Y = n n ~ Iml + 1. The radial function is given by . R( p) = e-p/2pltniP(lm l
'Since 'Y = n -
!, we
+
1 - n , 21ml
+
= 1,2,3, ... and
1; p)
(A .93)
n=1,2,3, ...
(A.94)
find the energy levels
E ri =
Using the relations
(n!)2
m
Lm(z)
=
(-1)
m!(n-m)!
n
F[
-en - m),m + l;z]
(A.95)
and 2 (n+m)! e-pp2m[L~:m(p)] pdp = (2n + 1 ) - - o (n-m)! 00
1
(A.96)
we obtain the normalized radial wave function Rnm(r) satisfying
(A.97)
.-
4!
(n - Iml - I)! a o V (2n - 1)3(n + Iml- I)! .'
x e- p/ 2p lmIL 2Iml (p) 11+1171 1- 1
4
(n + Iml - I)!
ao
(2n-1)\n-lml-l)! e- p /
X
2
(2Iml)! p1m1p( -n + Iml + 1, 21ml + L; p) (A.98) 2r
p=
(n - t)a o
n =1,2,3, ...
and
Imls:;n-] (A.99)
A.2
TV,'O-DIMENSIONAL (2D) CASE
647
The complete wave function is (A.IOO) As r ~ 0, Rnm(r) ~
p1ml,
which does not vanish only if m
It/Jno(r
=
0)1
=
2 1 IRnO(O)1 27T
-
- --
2
=
O. We obtain
1
(A.lOl)
------::-
7Tao2 ( n - '21)3
The above result is l/(n - i)3 per area of the circle determined by the Bohr radius Qo' .. Case 2: 2D Continuum State Solutions (E > 0). The procedure similar to that in the 3D case:
IS
very
(A.I02) p
= 2iKr
=
(A.103)
We chce 1 = IK ]I
and define ~
=
.-
\ " ,
rI Q o again. The radial function Ri p) behaves like
R(p)
=
Canst.
e-p /2p lmIF
.' l '
( Iml + 2 + ~, 21ml + 1; p
)
(A.I04)
i
If we assume that
and follow the same steps as that in the 3D case, we obtain
~ (2Iml)! err/(2K)
N
= « m.
-
7T
(
1
i )
2
K
r Iml + - + -
(A.106)
··· n
.,~ .
· . ' r, ~
. ...-1'"O"'~ .. - - "O;" ~.
- :... ~ ,
-r,,,,,• •': _ ~
" ".',~ - "i ~'"
648
.~
.._. """'. ' _ _. •_ .
THE HYlJROGEN ATOM C3D A ND 20 EXCITON STA"j'ES)
and R'(I/!) satisfies the (j(K - K') normalization rule
(A.107)
The only minor difference between the 2D and 3D radial wave functions is that in 2D, as r ---+ co, the prefactor in front of the cosine function is given by
l l{i.
-
(A.I08a)
where
fT e N Km{2Iml) ! V-;; If(lm l + i
-'TT j{ 2 K)
b,m l
=
«: ~
(Iml +
~):
.
+ ilK) I
+ arg [ r ( ml +
~
+
(A.108b)
~)]
(A.108c)
and bKm = -/2 1Tr is determined by the 8(K - K') normalization rule. If we change back to the physical quantities in the real space r instead of the normalized dist ance v = rlao, and use the 8(E - E') normalization rule, noting that
.(A .109)
.'
we find for
(A .lJO )
RKm(r ) /2KR y «;
(A.lIl)
A.2 TWO-D iM ENSIONAL (2D) CASE
Using
r( 1+ K)i ~ r(1
i)
2
2
+ K
2
r(1
~o J
2 -
cosh( 7T /K)
(A.112)
and
1
r[lml + 2 +
i K
)
2_
n
[(s _ ~)2
+ 1]
s = 1 2 K2
(A.113)
7T"
cosh ( 7T /
K)
we obtain
CE'( ) (2kr)lml ., e -ihF ( 1· J f2R; Iml + - + -'- , 21ml + 1; 2ikr 2R a 21ml ! 2 y
K
o
(A.114a)
(Ao114b)
Note that E = h 2k 2/2mr> and tion is given by
K
= k/ k ; =
ka o . The complete wave func-
(}\.115) The wave function approaches (2kr ) Iml as r except for m = 0:
0, and it vanishes a
---+
r
=
°
.'
2 /
1 -
- - - ; ; - - - - ; : - --
-
-
-
-
R }' a ~ 2 7T" [1 + exp( - 2 7T" /
-
"7"
K) ]
Important results of this appendix are summarized in Table 3.1.
(A.116)
650
THE HYDROGEN ATOM (3D AND 2D EXClTON STATES)
REFERENCES 1. For both bound and continuum state solutions in the three-dimensional case see L. D. Landau and E. M. Lifshitz, Quantum Mechanics, 3d ed., Pergamon, Oxford, UK 1977, p. 117, and H. A. Bethe and E. E. Salpeter, Quantum Mechanics of One- and Two-Electron Atoms, Springer, Berlin, 1957 . 2. For an n-dimensional space, n :2: 2, see M. Bander and C. Itzykson, "Group theory and the hydrogen atom (0 and (IO," Rev. Mod. Phys. 38, 330':..-345 (1966), and 38, 346-358 (1966). 3. C. Y. P. Chao and S. L. Chuang, "Analytical and numerical solutions for a two-dimensional exciton in momentum space," Phys . Rev. B 43, 6530-6543 (1991). 4. E. Menzbacher, Quantum Mechanics, 2d ed., Wiley, New York, 1970. 5. H. Haug and S. W. Koch, Quantum Theory of the Optical and Electronic Properties of Semiconductors, World Scientific, Singapore, 1990.
.'
Appendix B Proof of the Effective Mass Theory B.!
SINGLE BAND
To prove the effective mass theory (4.4.5) in Section 4.4, let us write the Bloch function
(B.l) satisfying (404.3). Since {l/Jnk(r)} is a complete set of basis functions, we may expand the solution l/J(r) in terms of these functions:
l/J(r)
=
Lf n
=
B.Z.
Lf n
B.Z.
d 3k
(27T)
3anCk)l/Jnk(r)
d 3k
(27T)
. 3
(B.2)
a n(k) Ink)
where the integration is over the first Brillouin zone (BZ) in k space. Multiplying (4.4.4) by l/J:k(r) and integrating over the Volume, we find \,
where
(Bo4) and the orthonormal relation (nkln'k') = us consider the Fourier expansion of Utr)
s; n,8(k -
k') has been used. Let
,
(B.5) 651
PROUF OF T HE
652
EFFI~CTIVE
MASS THEORY
We find
(B.6) Since the product u~k(r)un'k,(r) is periodic in r, we may expand this product in terms of a Fourier series u~k(r)Un'k,(r)
=
E C(nk, n'k' , G)e iG '
r
(B.7)
G
where G sums over all reciprocal lattice vectors. Therefore, ( n k IV In' k') =
E C ( n k , n' k' , G) [;
k - k' - G
(B.8)
G
Here k and k' are in the first Brillouin zone. We assume the following: 1. The perturbation !V(r)1 is small enough that there is no mixing between the bands (single-band case, n = n''). 2. VCr) is slowly varying in r. Thus O, is falling off rapidly for large k,
(B.9) or equivalently, Ll~kLlnk' = 1 is assumed. 3. The integration over k is mainly contributed from k = k o (an extremum or zone center) since we are interested in the behavior of energy near ko' For convenience , we take k o = O.
.-
The resultant equation for a)k) becomes .' (B.lO)
Define an envelope function F(r)
(B .ll) We obtain [E n ( -iV) + U(r)]F(r) = EF(r)
(B.12)
from the inverse Fourier transform of (B.lO). The above equation is the effective mass equation in real space.
B.2
DEGENERATE B/\.NDS,
653
The total wave function is
fa
=
(k')eik'· r
d 3k'
u .o( r(217)3 )-nk
ri
(B.13)
F(r)unko(r)
=
using the leading order approximation for unk(r). Using the k . p theory in Section 4.1, we have
EnC k )
En(O) +
= .-
I: Da{3kak{3
a,
p
(B.14)
Thus, the effective mass equation can also be written as
[L
a,p
d_)
D {3 ( _i_d ) (_i_ CX
dX cx
+ U(r)]F(r)
=
[E - En(O)]F(r) (B.I5)
dX{3
where Da{3 is given by (4.1.13). Alternatively, Da.{3 = (h 2/ 2)( 1/ m * )a{3 ' and we can write (B. 15) as the effective mass equation (4.4.5).
B.2
DEGE!'lERATE BANDS .~
To prove the effective mass theory (4.4.11) for degenerate bands [1], we choose a complete set of basis functions: (B.16) Expand the wave function !/fer) for (4.4.9) in terms of these basis functions:
(B.17) We proceed as before and obtain
654
PROOF OF T1 [E EFFECTIVE
MASSTHE01~Y ,
For the choice of the basis functions as in Section 4.3 for the Luttinger-Kohn Hamiltonian, Pji = 0 for all i, j = 1, ... ,6. That is why we have to go to a second-order perturbation theory. Define,
(B.19) We obtain in k space
[E - Ej(O)JaJk) (B.20) Therefore, we obtain the effective mass equation in real space:
t [E D/;P( -i~ I(_i_a
j'=1
a,f3
\
aX a I
J + v(r)OJJ']Fj,(r)
=
[E -
Ej(O)JFj(r)
aXf3
(B.21) where 2
D':'~
))
h [ = -- 0
2m o
0
0
,(5
11
af3
+"
p?' pf3.. J'Y
'YJ
+ p~rt pa" 'Y1
]
c: m 0 (E 0 - E y ) 'Y
(B.22)
and the wave function in the effective-mass theory is given by 6
ljJ(r) =
E Fj(r)ujo(r) . .' j= 1
(B.23)
\
for the leading-order approximation for ujk(r) =:: ujo(r). Notice that if VCr) == 0, the solution to (B.2}) is indeed the plane.' wave function, that is, Fj(r) = a /k)e ik· r, j = 1, 2, ... ,6, where {a j(k), j = 1, ... ,6} is an eigenvector of (4.3.16).
REFERENCE 1. J. M. Luttinger and W. Kahn, "Motion of electrons and holes in perturbed periodic fields," Phys. Rev. 97, 869-883 (955).
Append.ix C
Derivations of the Pikus-Bir Hamilton-ian for a Strained Semiconductor In this appendix, we derive the Pikus-Bir Hamiltonian [1, 2] discussed in Section 4.5. Using the coordinate transformation between the uniformly deformed coordinates and the undeformed coordinates (4.5.2) and (4.5.4), we obtain 3
r;
=
ri
+ ~
C i j rj
(C.la)
j = l
noting that both (x', y', z') and (x, y, z ) are components using the same basis h " y, '" an d'" vee t ors x, z, were r 1 = x, r 2 = y, T 3 = z, an dr'1 = x," r 2 = Y, , T; = z'. For example, x' = x + cxxx + cxyY + ExzZ. In a one-dimensional case with strain along the x direction only, we have E xx = (x' - z ) / x and Cr y = C x z = 0 . If a shear-type strain is introduced, in the x-y plane, we have E x y = (x' - _\ .' y, when E x x = E .r z = O. In vector form, we have r'
=
r
+£.r
(1 + £) . r
=
(C.lb)
The inverses of (Ci l a) and (C.lb) are
r.
=
r; - ~ cijrj
(C.2a)
j
r =
(1 -
~)
. r'
(C.2b)
In the uniformly deformed crystal, the potential is still periodic except that the function VCr') is a different potential from Vo(r). We write the Schrodinger equation for the Bloch function in the deformed crystal coordinate system r':
(C.3) 655
•
656
PIKUS-BTR EAMILTONI AN
pan A STRt-\fNED <)EMICONDU,CTOR
Using the chain rule and (C.2b), we have
orj a
or' I
a
a
L - - = - - L£jj -a . ar~ ar. Br,I . r), J J I
(CAa)
)
or p'
= p . (1 - e)
(CAb)
Similarly,
(C.S) The periodic potential can be expanded as
V[(l + s) . r] = Vo(r) + L f/;jCjj
(C.6)
i, j
-
. .. .
where
Therefore, Eq. (C.3) becomes (C.7)
where (C .8)
(C.9) Noting that we intend to treat He as a perturbation due to strain, and H o contains Vo(r) with a period equal to that of the undeformed crystal, we write the Bloch function as
l/!nk,[(1 + s) . r)
=
eik"r'unk,(r')
= eik"(I +E')'runk,[(l + s) . r] =
eik'ru~k(r )
(C.IO)
where k = (l + s) . k' ha s been used, and we rename undO + e) . r] as u~k(r), for the strained Bloch periodic part, which is to be determined .
C.lSINGLE-BAND CASE
657
Substituting (C.IO) into (C.7), we obtain Ho[eik'ru:;k(r)]
(C.Il) (C.12)
Therefore, we have the equation for the wave function u~/r):
(C.13a) (C.13b) (C.13c) (C.13d) (C.13e) The above result is similar to that in the original paper of Pikus and Bir, if we note that k' = (1 - £) . k. Our conventions are that primes k' and r' are used for the deformed crystal and k and r are used for the undeformed crystal. Since the perturbatior term H k vanishes in the first order (Hk\m = 0 because of parity considerati .1, we seek perturbation terms second order in k and first order in CaW
C.l
SINGLE-BAND CASE
For example, a single conduction band is probably the simplest case. The perturbation theory for the single subband leads to U~k( r)
= u n O( r)
Houno(r) = En(O)unO(r) h h2 (k . p) (k' p ) . En(O) + - - + (HJnn + - 2 L nn' . n'n 2rn o rna n'*n En - En' fz " (k : p) nn' ( H fJ n'n + (He) nn' (k . p) n'n 2k 2
E
=
+-
LJ
rna n'*n
=
En(O) + (Hc)nn +
( C.14a)
En - En'
LD
Ct{3k
ak{3
(C.14b)
a,/3
where
Da{3
is the same as (4.1.13). We have used the fact that the term in the
658
PIKlJ~ ·_PIR
HAMlf TC.':'iIAN FOR A STP..AINED
Sf~MICONDtJ: ~TOR
perturbation theory
where H' = (fl/mo)k . p + He + H ek, has nonzero contribution only from the first term (Ii /mo)k . p because of parity consideration, and we keep terms up to the second order in k and the first order in e. The diagonal term (nIH"ln) leads to ( C.15) because of the isotropic nature of the conduction band edge. Therefore, the single-band (conduction band) strained dispersion relation is given by
(C.16 ) and ( C.17)
C.2
DEGENERATE BANDS
We assume in general that A .
.-
B
Laj(k)u;o(r) + Lay(k)uyo(r) j
(C.18)
y
as in Section 4.4, where class A consists of those bands of interest, such as the degenerate valence bands: two heavy-hole, two light-hole and two spinsplit-off bands. Class B consists of those bands outside of class A. We follow the same procedures in Lowdin's perturbation method presented in Section 3.6 and obtain H' H' iv vi' E E 0 y
(C.19a)
E Oy ) aj' ( k) = 0
(C.19b)
A U} ·,=H.+ j}j
LB v rii'
A
L (Lj; /
from 0.6.12) and (3.6.5), respectively. The result turns out to be almost the
C.2
DEGENERATE BA1'\DS .
6"::9
same as that in the Luttinger-Kohn Hamiltonian: u~, Jj
=.
0.·,£-(0) + ~ '" DCi~k jJ J 11 a k{3 a,{3
(C.20)
or
H
=
H
LK
+ He
(C.21)
=
The first two terms in (C.20), E/O)ojj' + La,{3Dj~~kak{3 H j7!'" are exactly the elements of the Luttinger-Kohn Hamiltonian, and have been expressed in matrix form in (4.3.14). The third term in (C.20)
( H ) 11.., = E
jjCi~E: {3 J1 a
'~ "
(C.22)
a,{3
is the linear strain Hamiltonian. The last term in (C.20) vanishes for a lattice of diamond type, in which there is a center of inversion, and either Ph or (H)'Yj vanishes. For crystals that do not li:e a center of inversion, this term may not be zero. It means that an extremum in k space can be shifted due to deformation. However, this term is considered negligible for most III- V .compounds, We can also express the third term due to strain by identifying \,
(C.23a) Therefore [3],
h2 Y l -2m o
~Dd = u
h2 y z
-2m o
h2 Y 3
-2m o
Du ~
3
D'u ~-
3
-al-'
- -
(C.23b)
b -
2
(C.23c)
-d -
213
(C.23d)
PJKUS-BIR j-1,\MJ: ,,01\;1 AN FOR A STRAINFD SEMICONUJCjOP
660
where the constants D td , D t l , and D:/ come from different components of D/;r In matrix form, we have [3, 4] 1
P+Q
-S
R
0
--s fi
fiR
If, f>
-s+
P-Q
0
R
-fiQ
Ifs
R+
0
P-Q
S
{fs+
fiQ
If, ~) I~ _ 1.)
1
R+
s+
P+Q
-fiR +
--s+ fi
--S+
- fi Q
ffS
-fiR
P+~
0
fiR -+-
{fS+
fiQ
--S
0
P+~
H=-
0 1
Ii
1
Ii
2'
11
2'
2
_1) 2
It, t> 11.2' - 1.) 2 (C.24)
where P = P,
+P
E
R = R; + R B
Q = Qk + Q S = Sk
+
SE
B
(C.25a)
(C.25b) .'
PE = -
a
L' (
E: x x
+
E: y y
+
E: z·z )
( C.25c) where the wave vector k is interpreted as a differential operator - iV'; cij is the symmetric strain tensor; Yl, Y2' and Y3 are the Luttinger inverse mass parameters; au' b, and d are the Pikus-Bir deformation potentials; and A is the spin-orbit split-off energy. The basis function I i, rn) denotes the Bloch
REFERENCES
6Gl
wave function at the zone center and is listed in Eq. (4.3.3). Here the energy zero is taken to be at the top of the unstrained valence band. The Hamiltonian (C.24) has been used extensively to study the strain effects on the band structures of semiconductors.
REFERENCES 1. G. E. Pikus and G. L. Bir, "Effects of deformation on the hole energy spectrum of germanium and silicon," Sov. Phys i-Solid State 1, 1502-1517 (1960). 2. G. L. Bir and G. E. Pikus, Symmetry and Strain-Induced Effects in Semiconductors, Wiley, New York, 1974. 3. S. L. Chuang, "Efficient band-structure calculations of strained quantum wells using a two-by-two Hamiltonian," Phys. Rev. B 43, 9649-9661 (1991). (Note that au in this paper should be taken as -au to compare with data in the literature.) 4. C. Y. P. Chao and S. L. Chuang, "Spin-orbit-coupling effects on the valence-band structure of strained semiconductor quantum wells," Phys. Rev. B. 46, 4110-4122 (1992).
!
Appendix D Semiconductor Heterojunction Band Lineups in the Model-Solid Theory [1] Semiconductor heterojunctions and superlattices have been under intensive investigation both theoretically and experiment ally for th e past three decades. The potential device applications using heterojunctions are tremendous. In this appendix, we discuss a simplified model to determine the energy band lineups of semiconductor heterojunctions based on the model-solid theory . Jl -4]. The goal is to develop a reliable model to predict band offsets for a wide variety of heterojunctions without the need for difficult calculations such as in the local-density-functional theory or ab initio pseudopotential method. The relation of the model-solid theory to the fully self-consistent first-principles calculations can be found in Refs. 2 and 3. The major idea is to set up an absolute reference energy level. All calculated energies can then be put on an absolute energy scale, allowing us to derive band lineups. In the model-solid theory, an average energy over the three uppermost valence bands (the heavy-hole , the light-hole, and the spin-orbit split-off bands) E u • av is obtained from theory and is referred to as the absolute energy level. The values of E; av for different semiconductors are usually tabulated [1] (Table K.2 in Appendix K) so that no calculations for these values are necessary. These results should be compared with those of the first-principle calculations whenever possible to justify the model. An . estimate of the maximum possible error is about 0.1 eV. Band offsets should be checked with experimental data such as those in Refs . 5-19. The modelsolid theory provides a simple guideline for estimating the band offsets for materials, especially ternary compounds with varying compositions for which experimental data may not be always available.
D.I
UNSTRAINED SEMICONDUCTORS
If materials A and B have the same lattice constants, we may have an ideal heterojunction and there is no strain in the semiconductors. For this case, the heavy-hole and light-hole band edges (E H H and E L H ) are degenerate at the zone center, and their energy position is denoted as E u : ~
E L• 662
-
EV , 3V +
3"
(0 .1)
D.I
UNSTRAINED SEMICONDUCTORS
. 663
where ~ is the spin-orbit splitting energy, and the spin-orbit split-off band-edge energy E so is 26-
(D.2)
3
The conduction band edge is obtained by adding the band-gap energy E g to
e; (D.3) Note that in the model-solid theory, the spin-orbit splitting energy 6- and the band-gap energy E g are taken from experimental results. The only input provided by the model-solid theory is the tabulated Eu,av value. This Eu,av value is essentially the same as the p-state energy E p in Fig. 4.3a. With the above results, the band lineups between materials A and Bare shown in Fig. D.l. We have
and the band-edge discontinuities are
6.E c
E cA
=
-
E cB
6.E v
tx E; + 6.E u
=
E yB
-
E vA
6.E g
=
(D.4) (D.5)
The partition ratios of the band-edge discontinuities, Q; = 6.E e/ilE g and Qu = 6. E u / il E g' are obtained from this theory and can also be compared with experimental data.
. \\
.'
-
Material A
-
-
-
-
-
E~
-
Material B
Absolute - - - zero energy
- -
t L\E c
E~
I
B
Eg
A
Eg
___ ~ 3_
L\E y
- -
tJ.A
E~,av -
"3
-
- -
-
Figure D.l. Band lineups in the model-solid theory, E" ,",v in each material region is obtained from the model-solid theory and is tabulated in Appendix K. The bandgap energ-y E g and the spin-orbit splitting A ofeach material are taken from experimental 'results.
., I
"
! :1 !
664
D.2
13'\ND UN'El7?:: IN THE MODEi SOLiD THEORY
STRAINED SEMICONDUCTORS
If a material A with a lattice constant a is grown on a substrate with a lattice
constant a o along the z direction, we have Ex x
=
Ey y
=
ao - a
(D.6a)
a
and
Cl2
- 2C- £ xx
(D .6b)
11
The band-edge shifts are (D.7a) (D.7b) The position of the average energy of the valence bands £0 av under strain is shifted from its unstrained position £~, av in (D.n by - Pe: ' .
(D.S) We thus have the center of the valence-band-edge energy
(D.9) The heavy-hole, light-hole, and spin-orbit split-off band edges are
E HH = E ~ - P, E LH = £~ - PE: E
so
d. I
lL\
2
(D.10) Qe 1 + 2 + 2"[L\2 + 2L1Qe + 9Q;f / 2
=£0 _ P _ L\ + Q e U E: 2 2
_
!-[L\"2 + 2L1Q + 9Q"2] 2 e e
1/
2
(D.l1) (D.12)
The conduction band edge is shifted by P, given by (D.7b):
(D.l3) Note that in the limit of a large spin-orbit split-off energy L\ » IQel, we can ignore the coupling of the spin-orbit split-off band and £Ll-l
=='
£,0 - P,
+ Qe
E so """ £,0 - P, - L\
( D.14a) . (D.14b)
D.2
STRAINED SEMICONDUCTORS
665
For a ternary alloy such as A x B I-xC with a lattice constant a(x), a(x)
=
xa(AC) + (1 - x)a(BC)
(D.lS)
which is a linear interpolation of the lattice constants a(AC) and a(BC) of the binary compound semiconductors, we use the following formula to calculate an energy level E (= EL~, av for example): E ( A x B 1 -x C) = xE ( A C) + (1 - x) E ( B C) b.a
+ 3x(1 - x)[ -av(AC) + auCBC)} -
ao
(D.16)
where the last term accounts -for a strain contribution to the ternary alloy, 'I'. and S:« = a(AC) - a(BC) is the different between the lattice constants of two compounds AC and BC. Once E~, av is determined the- b a n d - e d g e r energies for the strained ternary compound can be calculated following I (D.6)-(D.13). Many theoretical parameters for the electronic and optical properties such as those listed in Table K.2 in Appendix K can be found in the data books compiled by various groups (such as Refs. 20-23), review papers (such as .t Refs. 24-27), and research papers (Refs. 28-37). Example Ga As/ 'Al As Heterojunction GaAs and AlAs have almost the same lattice constants. Therefore, the heterojunction has a negligible strain. We see from Table K.2 in Appendix K that
Et.,avCGaAs)
=
-6.~2
Ev,av(AlAs)
=
-7.49 eV, b.(AlAs)
eV, b.(GaAs)
= =
0.34 eV, Eg(GaAs)
=
1.52 eV
0.2S e V, Etr(AlAs)
=
3.13 eV
.'
Therefore,
EuCGaAs) -
0.34 -6.92 + - 3
=
-
E[:(AlAs)
=
0.28 -7.49 + - 3
=
-7.40 eV
6.E v
=
-6.81 + 7.40
Also, the band-gap discontinuity is b.Eg discontinuity ratio is b.Et./b.Eg = 0.37.
=
6.81 eV
0.59 eV
1.61 eV, and the valence-band
=
•
BAND LlNFUPS H' THE l\nnEL-SOLID THEORY
666
Example
InO.53GaO.47As /InP Heterojunction
a(GaAs)
o
=
a
a
5.6533 A, a(InAs) = 6.0584 A, a(InP) = 5.8688 A
E u,3v(In 1 _ xGa xAs) = xEu.av(GaAs) + (1 - x)Eu,av(InAs) Aa
+ 3x(1 - x)[ -av(GaAs) + aJlnAs)]a
Aa = 5.6533 - 6.0584 = -0.4051
A
a(In1_xGaxAs) = xa(GaAs) + (1 - x)a(InAs) A(In1 _xGaxAs)
= xA(GaAs)
+ (1 - x) 6.(InAs)
For x = 0.47, In0.53Ga0,47As is lattice matched to InP. Therefore, we do not have the strain terms (Pe = 0, Q e = 0). We obtain Eu,av(Ino.53Ga0.47As) = -6.77CJ eV, 6. = 0 .361 eV
Using Eu,av(InP) = -7.04 eV and EvOnP) = -7.003 eV, we find AEu = 0.344 eV. From room temperature data for the band gap, EgClno.53Gao.47As) = 0.73 eV, E/lnP) = 1.35 eV, and AEg = 0.62 eV, we obtain the ratio AEu/AEg = 0.55 = 55%. •
D.3 SOME EXPERIMENTAL REPORTS ON BAND-EDGE DISCONTINUITIES There has been a considerable amount of experimental data on band offsets, mostly on unstrained systems. For strained semiconductors, the band offsets are complicated by the deformation potentials, which also shift the conduction and valence-band edges. Therefore, fewer data are available for strained heterojunctions. .'
Eg(GaAs) = 1.424 eV
(300 K)
r
Eg(AlxGa1_xAs) = 1.424' + 1.247x eV
(300 K)
6. E g ( x) = 1.247x eV AEc = 0.67 AEg
A E L = 0.33 AEg
(AE c =0.69 AEg, AE v
== 0.31AE", Ref. 11)
D.3
EXPERIMF~TAL
REPORTS ON BAND-EDGE DISCONTINUITIES
667
2. Ino.53Ga0.47As/lnP ('" 0 K) [18]
E g ( lnP)
=
1.423 eV
Eg(InO .53Ga0.47As)
=
0.811 eV
. .t1Eg
=
0.612 eV
6. E c
=
0.252 e V
=
0.41 6. E g
se;
=
0.360 eV
=
0.59 t1E g
,
3. In o.52Al O.4S As/ InP( '" 0 K) [18] Eg(lnP)
=
1.423 eV
Eg(lno.52Alo.4SAs)
=
1.511 eV
t1E g
=
0.088 eV
t1 E;
= 0.252 eV = 2.86 t1Eg ,
t1E v
=
-
(Type II)
0.164 eV
The above results for Ino.53Ga0.47As/ InP/ In o.52 AlO.4SAs band offsets and their transitivity relations are illustrated [18] in Fig. D.2. The transitivity relations give ts E; = 0.504 eV = 0.72 t1E g , and ts E; = 0.196 eV = 0.28 6.E g for an Ino.53Ga0.47As/ln0.52Al0.4SAs heterojunction. .~
t
0.252eV
0.504 eV 0.252eV 0.811eV
1.423 eV
1.51leV
/
O.SUeV
O.3dn j---J.64~V rlO.196~V Band offsets and transitivity of Ino.53GA0,47As/lnP (!1E c = 0.41 !1E g , !1E L. = = 2.86 ti.E g > !1E g = 0.088 eV) at low temperatures (0 K) [18].
Figure D.2.
0-59 tJ.E g ) and Ino.52AI0,48As/lnP (tJ.E c = 0.252 eV
~, ~
..
~""""",_",_."""~ ._,,,~_,
_~
..
~_.
__ •."",
...., .•'
-.1
,,' ...•
_~
•. ":"., .. , .. _
,',.
~r
' .. 'l .·.~~'7'
\.~"
"J"'l-~t'.o..j:""""~.":f'_.Y"· ·
,'
--""~,"""_r;'.-
,~-
~~,
,w~_.~
·~.'
iJ/.ND :,TNEliPS IN 'fEE MODEL-SOLlD
668
_.
··· ·.,···' - : '"!""' :r,..· ·-...·,.~ ·•__••··..~···'!~
THEO~Y
4. In 1 _x G a xAs v PI-V/ InP lattice-matched system [22] For Inl_XGAxAsyPI_Y quaternary semiconductor lattice matched to InP substrate, 0.1896y X= - - - - - - - -
0.4176 - O.0125y E 8 = (Inl_xGaxAsYPI_Y) = 1.35 - O.775y.+ O.149 y 2 eV ~Eg( y)
= O.775y - O.149 y 2 eV
~Eu( y) = O.502y - O.152 y 2 e V
~Ec(Y) = ~Eg(Y)
where
~Eu( y)
- tlEv(Y) = O.273y + O.003 y 2 eV
was determined experimentally.
•
Some reports on strained InxGa1_xAs/lnP, InXGal_xAs/lno.52Alo.4sAs, InGaAs/InGaAsP, and In .Ga l -xAs /GaAs can be found in Refs. 7-9, 14, 15, and 19.
REFERENCES 1. C. G. Van de Walle, "Band lineups and deformation potentials in the model-solid theory," Phys. ReL'. B 39, 1871 -1883 (1989). 2. c. G. Van de Walle and R. M. Martin, "Theoretical calculations 0: semiconductor heterojunction discontinuities," 1. Vac. Sci . Techno!. B 4, 1055-1059 (1986). 3. c. G. Van de Walle and R. M. Martin, "Theoretical study of band offsets at semiconductor interfaces," Phys. Rev. B 35,8154-8165 (1987). 4. c. G. Van de Walle, K. Shahzad, and D. J. Olego, "Strained-layer interfaces between II-VI compound semiconductors," 1. Vac. Sci. Technol. B 6, 1350-1353 (1988). 5. R. People, K. W. Wecht, K. Alavi, and A. Y. Cho, "Measurement of the. conduction-band discontinuity of molecular beam epitaxial grown Ino.52Al0.4SAsj Ino.5JGao.47As, N-n heterojunction by C-V profiling," Appl. Phys, Lett. 43, 118-120 (1983). 6. R. C. Miller, A. C. Gossard, D. A. Kleinman, and O. Munteanu, "Parabolic quantum wells with the Ga As-Al Ga.Lj As system," Phys. Rev . B 29, 3740-3743 (1984). j
7. R. People, "Effects of coherency strain on the band gap of pseudomorphic Irr.Ga I -x As on (OOl)InP," Appl, Phys. Lett . 50, 1604-1606 (1987). 8. R. People, "Band alignments for pseudomorphic InP/In
T::"~
REFERENCES
669
10. C. D. Lee and S. R. Forrest, "Effects of lattice mismatch on In xGa l-xAs / InP heterojunctions," Appl. Phys. Lett. 57, 469-471 (1990). 11. L. Hrivnak, "Determination of r electron and light hole effective masses in Al xGa i . ... As on the basis of energy gaps, band-gap offsets, and energy levels in AlxGa1_xAs/GaAs quantum wells," Appl, Phys. Lett. 56, 2425-2427 (1990). 12. B. R. Nag and S. Mukhopadhyay, "Band offset in InP/Gao.47Ino.53As het-erostructures," Appl, Phys, Lett. 58, 1056-1058 (1991). 13. M. S. Hybertsen, "Band offset transitivity at the InGaAs / InAlAs / InP(001) heterointerfaces," Appl . Phys. Lett. 58, 1759-1761 (1991). 14. B. Jogai, "Valence-band offset in strained GaAs-InxGa1_xAs superlattices," Appl. Phys, Lett. 59, 1329-1331 (1991). 15. J. H. Huang, T. Y. Chang, and B. Lalevie, "Measurement of the conduction-band discontinuity in pseudomorphic InxGal-xAs/lno.52Al0.4SAs heterostructures," Appl. Phys. Lett. 60, 733-735 (1992). 16. S. Tiwari and D. J. Frank, . "Empirical fit to band discontinuities and barrier heights in III-V alloy systems," Appl. Phys, Lett. 60,630-632 (1992). 17. R. F. Kopf, M. H. Herman, M. L. Schnoes, A. P. Perley, G. Livescu, and M. Ohring, "Band offset determination in analog graded parabolic and triangular quantum wells of GaAs/AlGaAs and GalnAs/AllnAs," J. Appl. Phys. 71, 5004-5011 (1992). 18. J. Bohrer, A. Krost, T. Wolf, and D. Bimberg, "Band offsets and transitivity of InxGal_xAs/lnl_yAlyAs/lnP heterostructures," Phys. Rev. B 47, 6439-6443 (1993). 19. M. Nido, K. Naniwae, T. Terakado, and A. Suzuki, "Band-gap discontinuity control for InGaAs / InGaAsP multiquanturn-well structures by tensile-strained barriers," Appl. Phys. Lett. 62, 2716-2718 (1993). 20. K. H. Hellwege, Ed., Landolt-Bornstein Numerical Data and Functional Relationships in Science and Technology, New-Series, Group III 17a, Springer, Berlin, 1982; Groups III-V 223, Springer, B~rIin, 1986. ;
21. For a brief version of the data book in Ref. 20, see: O. Madelung, Ed., Semiconductors, Group IV Elements and I/I-V Compounds, in R. Poerschke, Ed., Da t a in Science and Technology" Springer, Berlin, 1991.' 22. S. Adachi, Physical Properties of III-V Semiconductor Compounds, Wiley, New York, 1992. 23. S. Adachi, Properties of Indium Phosphide, nTSPEC, The Institute of Electrical Engineers, London, 1991. 24. J. S. Blakemore, "Semiconducting and other major properties of gallium arsenide," 1. Appl. Phys. 53, R123-R181 (982). 25. S. Adachi, "Material parameters of In Ga l_xAs yP 1- y and related binaries," 1. Appl. Phys. 53, 8775-8792 (1982). j
26. S. Adachi and K. Oe, "Internal strain and photoelastic effects in Ga1_xAlxAs / GaAs and InxGal_XAsyPl_y/lnP crystals," 1. Appl. Phys. 54, 6620-6627 (1983). 27.S. Adachi, "GaAs, AlAs, and Ga1_xAlxAs: Material parameters for use m research and device applications," 1. Appl. Phys . 58, R1-R28 (1985).
[, i' r r
67U
BAND IJNEUPS If\: THE MODEL-SOLID THEORY
28. P . Lawaetz, "Valence-band parameters in cubic semiconductors," Phys, Rev. B 4, 3460 -3467 (1971). 29. R. E. Nahory, M. A. Pollack, and W. D. Johnston, Jr., "Band gap versus composition and demonstration of Vegard's law for In1_xGa xAs yP1 - y lattice matched to InP," Appl, Phys . Lett. 33, 659-661 (1978). 30. K. Alavi and R. L. Aggarwal, "Interband magneto absorption of Ino.53Gao.47As," Phys. Rev. B 21, 1311-1315 (1980). 31. A. Raymond, J. L Robert, "and C. Bernard, "The electron effective mass in heavily doped GaAs," J . Phys. C: Solid State Phys. 12, 2289-2293 (1979). 32. L. G. Shantharama, A . R. Adams, C. N. Ahmad, and R. J. Nicholas, "The k . P interaction in InP and GaAs from the band-gap dependence of the effective mass," J. Phys. C: Solid State Phys . 17,4429-4442 (1984). 33. W. Stolz, J. C. Maan, M. AJtarelli, L Tapfer, and K. Ploog, "Absorption spectroscopy On Ga0.47Ino.53As/AJo.4slno.52As multi-quantum-well hetero-structures . 1. Excitonic transitions," Phys . Rev. B 36, 4301-4309 (1987). 34. W. Stolz, J. C. Maan, M. Altarelli, L. Tapfer, and K. Ploeg, "Absorption spectroscopy on Ga0.47Ino.53As/Alo.4sIno.5zAs multi-quantum-well hetero-structures; II: Subband structure," Phys, Rev. B 36, 4310-4315 (1987). 35. L. W . Molenkamp, R. Eppenga, G . W. 't Hooft, P. Dawson, C. T. Faxon, and K. J. Moore, "Determination of valence-band effective-mass anisotropy in GaAs quantum wells by optical spectroscopy," Phvs, Rev. B 38, 4314-4317 (1988). 36. D. Gershoni and H. Temkin, "Optical properties of III-V strained-layer quantum wells," J. Luminescence 44, 381-398 (1989). 37. R. Sauer, S. Nilsson, P. Roentgen, W. Heuberger, V. Graf, A. Hangleiter, and R. Spycher, "Optical study of extended-molecular fiat islands in . lattice-matched In o.53Ga 0,47/\ <.;/lnP and InO.53GaO.47As/lnl_xGaxAsyPl_y quantum .ve lls grown by low-pressure metal-organic vapor-phase epitaxy with different interruption cycles," Phys, Rev. B 46, 9525-9537 (1992).
Appendix E Krarners-Kronig Relations The induced electric polarization P in a material is due to the response of the medium to an electric field E (ignoring the spatial dependence on r):
pet) =_cof~oox(t - T)E(T) d-r cofoox( T)E(t - T) d r o
=
(E.l)
The integration over T is from - 00 to t in the first expression, since the response p(t) at time t comes from the excitation field before t. In other words, the function X( T ) has the property that
<0
(E.2)
coE(t) + Pt z)
(E.3)
c(w)E(w)
(EA)
for
T
i.e., the system is causal. Since
D(t)
=
we find in the frequency domain
D(w)
=
by taking the Fourier transform of (E.3), where
(E.5) Since X( T) is a real function (it is in the time domain), we see that
c( -w)
=
c*(w)
(E.6)
If we write c(w) in terms of its real and imaginary parts,
c(w)
=
C'(w) + ic"(w)
(E.7) 671
KH/tvlFRS-KRONI(, HE] ATIONS
672
we find that e' ( -
w)
£/1 ( _
w) = -
e' ( W)
=
£" (
(E.8)
w)
(E.9)
that is, the real part of c(w} is an even function, and the imaginary part is an odd function of w. Another physical property of £(w) is that, in the highfrequency limit, £(w) tends to eo, because the polarization processes PC!), which are responsible for X, cannot occur when the field changes sufficiently rapidly [1]:
(E.lO) Define an integral I in the complex
Wi
plane,
I = _I_A:.. e( Wi)
27Ti':Yc
Wi -
£0
-
w
dw
'
(E.ll)
where the closed contour C is shown in Fig. E.1. It is in the upper Wi plane. The function e( w) is analytic in the upper-half plane, since when Wi = w R + iw j , the integrand in (E.5) includes an exponentially decreasing factor ewhen W j > O. Since the function X( T) is finite (for a physical process) throughout 0 < T < 00, the integral in (E.5) converges. Since the function e(w') - £0 is analytic in the upper Wi plane, the closed contour does not have any poles; therefore, the integral I vanishes using Cauchy's theorem. By breaking the contour into three parts-CO Oll the real axis, - R < Wi < w - 8, w + 8 < Wi < R, (ii) along the infinitesimally small semicircle near w with a radius 8, and (iii) along the big semicircle with a large radius R-we find that the contribution due to part (iii) is zero as R ~ 00. Therefore, as 8 ~ 0, the integration along part (i) is the principle W
{ 7"
-R Figure K!. The integration contour on the upper-half w' plane for the derivation of the Kramers-Kronig relation.
KRAMERS-KRONIG RELATIONS
. 673
value (denoted by P) of the integration along the real axis from and we obtain . 1.
- - p 27Ti
f oo -
00
+ --
dw'
w
Wi -
1
£0
c; ( Wi) -
f
Eo' ( Wi)
27Ti 0
£0
-
WI -
dw '
=
0
00
to
+ 00,
(E.12)
(tJ
The second integral equals - i[e(w) - eo], which can be evaluated simply by a change of variable from Wi to 8, Wi - W = 8e i 9 at a constant radius 8. We find 1 7Tl
E(W)-£O=-'p
foo
e(w') - eo I 0)
-00
w
-
dw '
(E.13)
. We separate (E.13) into real and imaginary parts and find 1
e' ( w) -
= -
£0
P
"( ) -
pf
7T
d WI
I
(E.14)
-ooW-W
7T
1 £w---
£"( Wi)
f cc
e
£' ( WI) -
00
0
I
W
-cc
-
d to I :.
(E.15)
W
The above results are the Kramers-Kronig relations, which relate the real and the imaginary parts of £(w) to each other. If we make use of the even property of the real part c'ew) and the odd property of the imaginary part £If(W), we obtain alternatively 2
e' ( w) - e 0
=
-
f oo
P
2w =
-
7T
pf
I
dw
Ow-w
7T
. e" (w)
Wi Elf ( W' ) ,2 2
oc
0
e' ( Wi) 2 W'
-
-
(E.16)
E
w2
0
dw'
(E.17)
In a homogeneous, isotropic medium with a complex permittivity function £(w) = £'(w) + iE"(w) and a permeability }-La, the propagation constant of an electromagnetic wave at an angular frequency co is
k(w)
=
wVf-Lo£(w)
=
wJf-Lo£o [£~(w) + iE~(w)r/2
=
-n
w c
(E.18)
\,
t,
~ .
674
KRI\ ~v1ERS ···KRONIG
". 'l. _W .. ;: . _ .
RELAT10NS
where we have used the real and the imaginary parts of the relative permittivity
e( w) erC w) e~(
w)
= -
e' ( w ) =
-
eo s~ (
So
w) -
s" (
w)
So
(E.19)
and the complex refractive index
n=n
+ ix
(E.20)
We obtain the relations
(E.21a) .
2nK = s~ (w)
-
... ,
(E.21b)
Here the real and the imaginary parts of the refractive index new) and K(W) can be expressed as
n 2 = %[ e~(w) + K2 =
t[ -e~(w)
Vs~\w) + 8~2(W) ]
(E.22a)
+ Ve~\w) + 8~\W) ]
(E.22b)
Experimental data for nand K of GaAs and InP semiconductors as a function of optical energy and wavelength are tabulated and plotted in Appendix J.
REFERENCE 1. L. D. Landau, E. M. Lifshitz, and L. P. Pitaevski i, Electrodynamics of Continuous Media, 2d ed., Pergamon, New York, 1984.
~"
........
_
.... . . . ~
Appendix F
Poynting's Theorem and Reciprocity Theorem F.l
POYNTING'S THEOREM
The power conservation is a very useful law. From Maxwell 's equations in the time domain .
-. ...
a at
vx
E
v x
H = J
=
--B
(F.l)
a at
(F.2)
+
-D
Dot-multiplying (F.r) by Hand (F.2) by E, and taking the difference , we obtain
v . (E x where 'V • (E x H) Poynting vector as
=
H)
=
a at
aD at
-H . -B - E . -
H . 'V x E - E . V
- E .J
(F .3)
X
H has been used. Define the
S=E xH
(FA)
which gives the instantaneous energy flux density (W/m 2 ) . For an isotropic medium, D = E:E and B = ,uH, the electric and magnetic energy densities are E:
' w =-E·E e
2
,u wIn = -H· H 2
(F.5)
Therefore, Poynting's theorem in the time domain is simply
a
V'S= --(w at e +wm )-E'J
(F.6) 675
676
POYNTING'S THEOREM AND RECIPROCFfY THEOREM
If integrating over a volume V enclosed by a surface S, we obtain Poynting's theorem in the form
(F.7) i.e., the power flow out of the surface S equals the decreasing rate of the stored electric and magnetic energies plus the power supplied by the source, - fffE' JdV. A complex Poynting's theorem can also be derived from Maxwell's equations in frequency domain:
v . (tE
X
H*) = -iwOE . D* - ~B . H*) - iE . J*
(F.8)
If J = J d + Jf , where J d accounts for dissipation, e.g., J d = O"E is the conduction current density in a conductor, we then have
1 ) w__ 1-1 V· ( -ExH* +i-(E'D*-B'H*)+-E'J*=---E'J* (F.9) 2 2 2 d 2 I where the right-hand side is the time-averaged power supplied by the source JI , and the terms on the left-hand side are the time-averaged power flux, the difference in the electric and magnetic stored energy density, and the time-average dissipated power, respectively.
F.2
RECIPROCITY THEOREM [1, 2]
Consider two sources J(1) and J O ) producing two sets of fields in the same medium described by D = e E and B = ,uH: E(I )
= -
V'
X
H(l )
=
V'
X
E(2)
a = - -B(2)
V' If we take E(2) •
H (2 ).
(Fi l Oa) -
(F.10b), we find
a at
vX
X H( 2)
E (I ) .
( F .10a)
-B(I)
J (l)
+
a
(F .10b)
- D (I )
at
(F.lIa)
at
=
a
J (2 )
+ - - D (2)
(F.lIb)
at
(F. l lb) and subtract by
H(l) •
(Frl La) -
F.2
RECIPROCITY Tl-jEOREM
677
Integrating over an infinite volume and using the divergence theorem, we obtain
rt:. (E(l) ~
X H(2) -
E(2) X
H(!)) .
dS
=
f
E(2) •
J (1) dv -
v
f
dv
E(l) . H(2)
v
(F.13) Using the property in which the surface integral on the left-hand side goes to zero as the radius of the surface goes to infinity, we obtain
f
E(2) •
J(1) du
=
VI
f
E(l) • J(2)
du
(F.14)
Vz
Since the two sources J I and J 2 are distributed over finite regions, such as those of two dipoles, the volume integrals are only over the regions of the. two sources VI and V 2 , respectively. E(l) and E(2) would then be the electric fields due to J(1) and J(2\ evaluated at the positions of the other sources· occupying volumes V2 and VI' respectively. This is the reciprocity relation. We may generalize the above relation to field solutions in two different media, described by t;C!)(r) and e (2)(r), and the same permeability j..L. We have, using the frequency domain representation,
(F.15) .'
If we integrate the above equation; over an infinite volume, we obtain similar relations to (F.14) except for the extra term due to the difference between two dielectric functions. However, if we apply the above relation to dielectric waveguide structures which are translationally invariant in the z direction, and integrate over only a volume of a disk shape with a thickness 6. z ~ 0 and a radius R ~ 00 (see Fig. Fvl ), we find I
111/' AdXdYd~'~ (If" + If" + n}· dS ffA' alz+Cl.z
i dx dy +
ff A . ( - i) d x d y atz
(F .16) where A = E(1)
X H(2) -
E(2) X H(l)
and the fields at SOX) vanish. Since
J(I)
670
POYNTING'S Tf fECRE i\,; I,ND REGPR OCiT \ TH LORLM
t---...I
f----""'\
Dielectric waveguides
v f\
f\
-z -4--+-
Z
Figure F.l. The volume V for the space be twe e n z and z + /).Z enclosed by the surface 5 = 51 + 52 + 5 00 for the derivation of the reciprocity relation for dielectric waveguide structures.
and J(2 ) are zero in the dielectric waveguides, we obtain a reciprocity relation for the waveguide: J
- ff(E (l)
X H( 2 )
-
Jz
E( 2 ) X H(l») . i dx dy f
= iw ff(
S(2)(X,
y) -
S(l)( X,
y)]E(l) .
E(\)"dx dy
(F.17)
I
REFERENCES 1. L. D. Landau, E . M . Lifshitz, and L. P. Pitaevskii, Electrodynamics of Continuotls Media , 2d ed. , Pergamon , New York, 1984. 2 . S. L. Chuang, "A coupled-mode formulation by reciprocity and a variational pr inciple," J. Lightwa oe Technol. LT-5, 5-15 (l98~), and "A coupled-mode theory for multiwave guide systems satisfying the reciprocity theorem and power conservalion, " 1. Lightwave Techno!. LT-S, 174-183 (987).
Appendix G Light Propagation in Gyrotropic Media-Magnetooptic Effects [1-3] In this appendix, we present a general formulation to find the electromagnetic fields with the characteristic polarizations of gyrotropic media. The magnetooptic effects are then investigated.
G.!
MAXWELL'S EQUATIONS AND CHARACTERISTIC EQUATION
The constitutive relations for gyrotropic media are given by [1] D
E·
=
E
o
(G.la)
~]
(G.lb)
B = jLH
.
(G.2) .'
One example is a plasma with an externally applied de magnetic field in the i direction: "
(G.3a)
£g
£,
~ ~
£0 [
w( :;~w~;) ]
(G.3b)
:~ 1
(G.3c)
£0 ( 1
-
where w
qB o m
=C
(GA) 679
680
PROPAGATION IN
GYROTRO[)I':~
IviEDj,\--MAG;'\TETOOPTIC EFFECTS
is the cyclotron frequency, and
(G.S) is the plasma frequency for a carrier density n. Here m is the electron mass. For the free carrier effects in semiconductors, the effective mass of the carriers should be used. Note that the geometry of the medium considered is rotation-invariant around the z axis. Thus, we may consider the propagation wave vector k to be in the x-z plane without loss of generality: k = xk ,
+ zk z
(G.6)
We repeat Maxwell's equations for plane-wave solutions here: k X E
=
wB
(G.7a)
k X H = -wD
(G.7b)
k· B = 0
(G.7c)
k' D = 0
(G.7d)
Using (G.7a), (G.7b), and (G.2), we obtain k
X
(k x E) = w,uk x H =
-W
2
J.t E . E
Or, equivalently, the above vector equation can be written in a matrix representation following Table 6.1 in Section 6.3 of the text:
\ -k z
o o
E~J[~:]
(G.S) {
We carry out the square of the matrix on the left-hand side, and move to the right to obtain , I
k; .
lW
W
-iW 2J.t E!!
2,u E
2
J.tE g
-kxk"
k,~
-k",k z
+ k; "- (J./p.E 0
[EX
0 k2 'x
-
W
2
J.tE z
l.
~: ~O
(G.9)
The dispersion relation is obtained by setting the determinant of the matrix
G.l
1'.1AXV/ECl'S EQUATIOJ'iS A:t
681
to zero for nontrivial solutions for the electric field, We obtain the characteristic equation after some algebra (k.~
+ k; -
W
4
W
2
fJ.- E) (
-W
J-L2E: ( k ; -
W
2
fJ.- Ek ; -
2J-L C ) z
W
2J-L E k ; z
+
4
J-L2EEz )
(G.lO)
0
=
W
Rewrite the wave vector k in terms of the angle () with respect to the z axis, k
=
ik x + ik z = ik sin
f)
+ ik cos
f)
and define the constants K
=
w"j J-LE
(G.lla)
(G.llb) (G.llc) Equation (G.lO) reduces to
(G.12) which has the form
The solution k 2 is easily obtained from
k
where
2 =
B + VB 2 -
-
-
-
-
2A
4AC -
-
(G.13)
6~ 2
PROPAG ATION IN G YR O'I R()P IC MED i A-MAUN ETOOPT1C EI'PE ::TS
Usin g (G .9) again , we have k 2 cos " e
-
2
K
'K g2 1 - k
2
sin
(G.14)
e cos e
o
where k ? is given by the two possible roots in (G.13). Since the above determinant of the matrix is zero, Eq. (G.14) contains three algebraic equations, which are linearly dependent. Using the second and the third equations in (G.14), we find
( G .15a) k 2 sin 2
=
k 2 sin
e -:-..K-;
(G .15b )
e COS.e
.
where two possible valu es of k 2 are given by the roots in (G.l3 ).
G.2
SPECIAL CASES
Case 1: e = 0 (the wave is prupagating parallel to the magnetic field). Equation (G .14) becomes
,
.-
k2
-
K
2
k2
2
"
- i K 152
1"K g
-
K
0 2
0
0
[EX] ~: .~ 0
0
(G.16)
- K z2
We have £2 = 0 , since
K; =1=
0
(G.17 )
and
(G ,18) We obtain two ro ots for k
2
,
(G.19)
.\
G.2 .::iP;2CIAL CA(;ES
683
Substituting the above roots back into (G.16), we find 2 +K g 2 1'K g
- +i
(G.20)
Combining (G.17) and (G.20), we see that if the wave is propagating parallel to the magnetic .field, the wave will be circularly polarized. Let us assume that the wave is propagating in the + i direction; we have either
( a)
( G.21)
the wave is left-hand circularly polarized (LHCP), or
(b)
(G.22)
the wave is right-hand circularly polarized (RHCP). Case 2: 8 = "'IT /2 (the wave is propagating perpendicularly to the magnetic field). Equation (G.14) becomes -K 2 'K g2 1 0
-iK g2 k? -
K
2
o o
( G.23)
0 .'
Possible nontrivial solutions for the electric field will be \,
( a)
(G.24)
If k 2 = K; is true, we find that Ex =0, E y = 0 from the first two equations in (G.23). Therefore, we obtain that the characteristic polarization is linear polarization in the z direction E = iEz and the propagation con:' stant is k = K, = WJJ.LE z . (b) - K 2(k 2 - K 2 ) - K; = 0, which leads to
(G.25)
If (G.25) is true, then k 2
"* K;,
E;
Ex
=
= 0, and K g2 - i -2 E K Y
(G.26)
684
PROPAC-iATION IN GYROTR()PIC MED :\ - --MAGNETOOl'T1C EFFEC,'S
The wave is generally elliptically polarized in the x-y plane with a propagation constant k = K 4 - K;) / K 2 . The wave vector is always on the x-y plane since (j = 7T /2. Furthermore, if E g = 0, the medium becomes uniaxial. Equations (G.24) to (G.26) show that either the electric field is polarized in the z direction and k 2 = K'1, or polarized in the y direction (since Ex = 0, E, = 0 from (G.26)) and k 2 = K 2. Both waves are linearly polarized propagating with different velocities. This birefringence is called the Cotton-Mouton effect.
J(
G.3
FARADAY ROTATION
Let us consider a slab of gyrotropic medium with a dc magnetic field applied in the +2 direction and the wave propagated parallel to the dc magnetic field. This is the special case 1, (j = 0, discussed before, and the two characteristic polarizations are left- and right-hand circularly polarized with corresponding propagation constants given by (G.21) and (G.22). Consider an incident plane wave as shown in Fig. G.1 with E = xEoe i h
(G.27)
Upon striking the interface at z = 0, the wave will break up into two circularly polarized waves: E =
E E (x - iy)_o eik,.,z + (x + iy)~eiLZ 2
2
(G.28)
These two circularly polarized waves propagate with two different wave numbers, k + and k _. As discussed b~fore, k ± = J-L( E ± E g ) . At z = d, we have
w-l
.' (G.29)
•
x E =x~Eoe ikz
k::: Figure G.!. A linearly polarized plane wave E incident on a gyrotropic medium experiences Faraday rotation after passing through the medium at z = d .
zk H y
REFI:RENCES
685
Thus, we have the ratio of the y component to. the
x component
of the
electric field E;
E
eik +d _
-
ei/cd
-leik+d+eik_d
·x
(G.30) which is a real number. Thus the electric field at z polarized making an angle
=
d is again linearly
(0.31) with the i axis. We conclude that the incident linearly polarized wave (in the i direction) is rotated by an angle eF at x = d, which is called the Faraday rotation. Since the Faraday angle eF depends on the difference between k + = wVJL(e + £g) and k_= WVJL(£ - £8)' the carrier density n and the effective mass of the electrons can be measured from the magnetooptic effects using the Faraday rotation as discussed above. Another setup is called the Voigt configuration for which the propagation direction is perpendicular to the direction of the applied de magnetic field zBo' The incident wave is chosen to be linearly polarized at an angle of 45° with respect to the static magnetic field. The transmitted wave does not experience a rotation; it becomes elliptically polarized, however. The phase angle or the amount of ellipticity is determined by the difference of the propagation constants of ·~he two characteristic polarizations, which is related to the plasma frequency W P and the cyclotron frequency we' For more discussions on the rnagnetooptic effects and their measurements in semiconductors, see Ref. 3.
REFERENCES 1. J. A. Kong, Electromagnetic Wave Theory, Wiley, New York, 1990.
2. K. C. Yeh and C. H. Liu, TheolY of Ionospheric Waves, Academic, !'jew York, 1972. 3. K. Seeger, Semiconductor Physics, Springer, Berlin, 1982.
;~.,
' ,....,.,"'
f':'~
.•._.~:-
~
_.h
_~....."
~~ .
•~ ~ "
_
_
Appendix H Formulation of the ImprovedCoupled-Mode Theory In Appendix F we derived a general reciprocity relation for waveguide systems. The relation is
a
az
ff
(E(l) X
= iw
H(2) -
ff [
E(2)
s(2)( x,
x
H(l») •
i dx d y
y) - e(1)( x, y)] E(l)
• E(2)
dx dy
(H .I)
where E(1)(x, y, z ) and H(l)(x, Y, z ) are a set of solutions in the medium described by s(l)(x, y) everywhere in space. Similarly, E(2)(x, y, z ) and H(2)(X, y, z ) are another set of solutions in another medium described by E(2)(X, y) everywhere in space. Let us consider three different media. Medium A:
Waveguide a Only
Suppose only waveguide a exists in the whole space (Fig. Hla). The medium is described by
The solution is
+ E~a)(x, y)] e i {3" z y) + H~a)(x, y)] e i /3 z
[E~{/)(x, y)
[H~a)(x,
(B.2) :
u
for the forward propagation mode and [E~a)(x, y) - E~{/)(x, y)] e- if3 " z
[ - H ~ a) (
X ,
y)
+ H ~a) (
x, y)] e -
(E.3)
i /3 a Z
for the same mode as (H.2) propagating in the - z direction. Note the 686
FORMULATION CF
~HE
IMPROVED COUPLED·MODE THEORY
(a) ___I
a
y_E(_a)c_x,y_)
687
_
------P:l~-----(b)
_Ia~,-(c)
_ "x
Figure H.1. Three different permittivity furictionsof interest for applications in deriving the improved coupled-mode theory using the reciprocity theorem. (a) only waveguide a exists in the whole space, (b) only waveguide b exists in the whole space, and (c) both waveguides a and b exist.
.'
relations between the field components of the forward propagation modes and those of the backward propagation modes. These relations can be obtained from Maxwell's equations and can also be checked from the z component of the Poynting vecto : for the power flow. We see that there is a sign change before H~a)(x, y) in CH.3). For example, the TE modes in a slab waveguide have a solution E = YE/x)e i {.1 Z and H = V X E/iwj.L = (-xi/3E y -+. zca/ax)Ey)/iwj.L for the forward propagation modes. T~e field expressions for the backward propagation modes are E = YE/x)e- ' {.1 Z and H = (xi/3E y + z(a/ax)E.)/iwf.L, with a sign change in the x component. Medium B:
Waveguide b Only
Suppose only waveguide b exists permittivity function is described by
III
the whole space (Fig. HcIb). The
The field sdlution is [E~b)(X, v)
[H~b)(x,
+ E~b)(x, y)] e i {.1 b z v) + H~b)(x, y)] e if3bz
(HA)
688
fORMULATION OF THE
jMP1~(iVEf) COUPl.ED-MODE
THE . )HY
for a mode guided in the z direction and
[E; b) (
X ,
y) - E ~b >< X , y)] e - i f3 b
[ - H~b)( .r ,
Z
y) + H~b)( x, y)] e -
(H.5)
if3b z
for the same mode as (H.4) propagating in the -z direction.
Medium C:
Both Waveguides a and b Exist-Coupled Waveguides
In this case, the medium is described by e(x,y)
which is shown in Fig. H.lc. The field solutions can be written as the superposition of two individual waveguide modes: E(x, y,
z) =
H(x, y, z)
=
a(z)E(a)(x, y) a(z)H(l1\x,
+ b(z)E(b)(x,
y)
y) + b(z)H(b)(x, y)
(H.6)
Let us consider three applications of the general reciprocity relation given by Eq. (H.n, which requires two sets of field expressions in two media, e(1)(x, y) and e(2)(x, y).
Application 1; ! Suppose we choose the first medium to be the coupled waveguide system described as medium C above, e(l)
=
e(x, v)
and the field solutions E(l) and H( l), as in (H.6), the coupled-mode solutions. Choose the second medium to be only waveguide a, e(2)(x, y) = e(a\x, y) and choose the solutions to be the corresponding guided mode propagating in .the - z direction (H.3). E (2) = [E ~ H(2)
(7 ) (
.r , y) - E ~') ( x, y)] e -
i /3,,:':
= [-H~a\x, y) + H~tl)(x, y)] e- iP,, 2
(R.7)
FORMULAT:ON OF THE IMPROVEr, COUJ>LEL'-!v'iODE THEORY
689
We obtain from the reciprocity relation (H.I)
dd Z
[f fac
z)e -
i~", ( - E~a, X H~'"
+ ffbCz)e-i~"'(-E~bl
X
-
E~a, X
ma' )
0
Z dx dy
H~a, - E~a' X H~b')
oZdXd Y ]
- iUJJf 6.c(G)(x,y)[E?a ). E~b) - E~a). E~b)] dxdyb(z)e- i ,l3 a z (H.8) Or d db(z) "d;Q(z) + C. dz = i(f3a + Kaa)a(z) + i(f3aC + Kba)b(z) (H.9)
where
(H.1D) 1 C p q = -ffE(q) x H {p) . i dx dy 2 I t
K pq =
w
4 Jf
.' (H .11)
~c(q)(x,Y)[E~P). E~q) -- E~P). E~q)] dxdy .'
(H.12) '
(H .13) I
Note that the fields have been normalized such that C aa 'an d Cbb
=
1.
Application 2
Choose e( l l( x , y), E(I) and H(l) to be the coupled waveguide system and the field solutions as in Application 1. Choose the second medium to be waveguide b only in the whole space
,. , ,. ,
~
~
_..-- --
.,
-
.
690
: • . , ..,,·t ....
F ORMU~ .ATION
,... ~_
·
p~
. ,; . . ..
"
" . • . .. . .
OF T H IC; ;:,1"1"'1<. ·. J'/2[' CC;UPLE D-M OO :-:
•
'i~HEO RY
with so lutions of t he guided mo d e propaga ting in the - z d ir e ct ion : E (2)
[E~b )(X , y) - E~b)(x, y) ]e- iJ3bZ
=
[ -H~b>Cx , y)
H (2) =
+
H ~h ) ( x , y) ]e-iJ3bZ
( H.14)
We obtain
Therefore, we fin d d dz
C-
[a(z)] = lQ . [a(z )] b(z)
(H. 16)
b(z)
where
c
=
[~ ~]
( H.1 7)
K aa
Q = [ ·r .1'" d b
(H.I S)
Application 3
Choose £(l)(x,
v)
E( 1) = [ E ~ a ) ( x I y) H (l)
£( G)(x,
=
+
= [H;U)(x, y) +
E~a)(
v)
x, y)] e il3 uz
H ~{f) ( x ,
y) ]e i13 uz
(H.19)
an d £ (Z)(x,
y) =
£(b )(X,
v)
E ( 2)
= [E ~ b ) ( X I v) - E ~b ) ( X , y ) ]e- iJ3bZ
H ( 2)
=
[ - H~b) (
x, Y)
+
H ~h l( x , v)
Je
- i13h2: .
(H.20)
•••- . ..- • •• , '"
'~
- .0::.'
••':':'" ~
FORMULATION OF THE LvIPROVED COUPLED-MODE THEORY
691
We obtain
(H.21)
(H.22) which is an exact relation. This relation also shows that for an asymmetric coupling system (f3 b =t f3 a), the coupling coefficients are not equal (K ba =t K ab). Only if the overlap integral C is small in the weak coupling case can K ba be approximately equal to K ab. Since
Qll =
e, + K aa
Q22 =
Q 12 = K ba + f3 aC Q21 = K ab
+
f3b C
e, + K bb
=
K ab + f3b C
=
K ba + f3a C
(B.23)
Q can also be written as (H.24) Therefore, d
[a(z)]
[G(Z)].
C ~ b( z)
= I[K + CB] b( z)
(H.2S)
0]
(H.26)
where B=[f3a
o
f3b
The coupled-mode equation can be written as d
[a(z)]
~ b ( z) M
=
. [a(z)] = 1M b ( z)
B + C-lK
(H.27) (H.28)
"i:jJa-;:IM
U
R.c"iSa·"-".-"
692
If
(H.29) th en 'Yo
=
'Y& =
Po
+
Ph +
K "" - CKba
1 _ C2 K bb - CK "b 1 _ C2
K ob - CK h b k a b = -------,-2
1- C
K b a - CK a a k b a = -------,,-2
1 - C
(H.30)
It is straightforward to show that (H.31) whi ch is an exact rel ation simil ar to (H .22).
Appendix I Density-Matrix Formulation of Optical Susceptibility The density-matrix theory plays an important role in applications to linear and nonlinear optical properties of materials in quantum electronics. The basic idea is that the density-matrix formulation provides a most convenient method to predict the expectation values of physical quantities when the exact wave function is unknown.
1.1
DENSITY-MATRIX THEORY [1, 2]
Assume that ljJ(r, t) is the wave function of the material system under a perturbation Hamiltonian, which can be due to an electromagnetic field or other excitations. The density-matrix operator p is defined as the ensemble average of the form
(1.1) where an overbar means the ensemble average. Explicitly, we can expand the wave function ljJ(T, t) using a complete set of wave functions ¢Jr): \, I
(1.2) n .'
Though not required, {¢n(r)} are usually chosen to be the solutions of the unperturbed Hamiltonian H 0' which describes the electronic states of the material system in the absence of any perturbation. The ensemble average of a physical quantity P is given by (P)
=
(ljJ(r, t)IPlljJ(r, t)
=.L: c:(t)cm(t) [m(r), P4>n(r)] In, n
=
L: Pnm Pm n m n i
=
Tr(pP)
(1.3 ) 693
DENSlTY-NiATfdX FORMULA.TIO:t' OF OPTICAJ SUSCEPTlBILITY
which is the trace of the matrix product Pnm and Pmn' where
Pmn
=
<4>m( r) IP! =
J¢~(r) P
Pnm =