7 OPTICAL GAIN ANALYSIS IN SEMICONDUCTOR...
Transcript of 7 OPTICAL GAIN ANALYSIS IN SEMICONDUCTOR...
123
7.1 Introduction
The gain-carrier-density and gain-current relations are considered as most important
parameters for the design and optimization of modern semiconductor diode lasers.
Therefore, many efforts have already been made to calculate the laser gain or the material
gain in bulk and low dimensional structures of semiconductor materials. The majority of
these theoretical gain models are developed considering the parabolic dispersion relations
of the conduction and valence bands [1, 2]. In reality, the band curvatures do not remain
perfectly parabolic at the energies away from the band edge. Nonetheless, the parabolic
gain model may be a good approximation for bulk GaAs- and InP based lasers used for
emitting light in the near-infrared spectral region. However, the narrow-gap InSb based
compounds have to be used for midinfrared applications, [3, 4, 5]. In these
semiconductors, the conduction band is highly nonparabolic and a reexamination of the
gain model is needed for proper investigation of laser operation. As for example, in
quantum-well structures of these materials, the valence-bands are considerablely
nonparabolic due to the band-mixing effect and the resulting gain spectra are significantly
different from those predicted by the parabolic band aassumptions [3, 6].
Moreover, as discussed in the preceeding chapters, due to the presence of
nonparabolicity in the band structure in the low dimensions the interband absorption
coefficients are seen to be significantly different when compared with their parabolic
band approximations. Higher rate of electron transitions in different subbands for photons
of same energy is expected because of availability of higher density of states arising in
non parabolic band profile. Again the separation between the energy subbands, formed
due to the quantization of energy levels in low dimensional structures, is more closely
spaced and as a result probability of transition will also be higher. Thus, the impact of the
conduction band nonparabolicity on the gain spectrum is investigated in this chapter in
semiconductor lasers of bulk state and their low dimensional structures. The interband
7 OPTICAL GAIN ANALYSIS IN
SEMICONDUCTOR LASER
124
absorption theory developed in the previous chapters for various nanostructures
considering the wave vector dependent optical transition matrix element (OME) on the
basis of three band energy model of Kane are applied to model the material gain of the
semiconductor lasers of various dimensions. The theoretical analysis is applied to diode
lasers of InAs, InSb, Hg1-xCdxTe and In1-xGaxAsyP1-y lattice matched to InP as examples
of gain medium because these compounds have been found to be the most promising
material systems for both the double heterostructure and the multiple-quantum-well lasers
operating in different ranges of infrared spectrum. A comparison with the conventional
parabolic band model is also performed. The obtained results show the necessity to
include the conduction band nonparabolicity in modeling of lasers based on narrow-gap
semiconductor materials.
7.2. Theoretical background
7.2.1. Formulation of the generalized optical gain for narrow band gap materials in
bulk state
The optical gain in a bulk semiconductor laser can, in general, be written as [2],
2 2
23
2
0
( )4
[ (
ˆ.
)
( )
( ) ( ) , ) ( ) (( ] ( ))h
bulk
o r
cvav
c c ve v
d k a p k
E k E k k E k E
eg
m cn
f f L k
(7.1)
where, is the angular frequency of the emitted or absorbed light, c is the velocity of
light in free space, r
n is the relative refractive index of the semiconducting material, 0 is
the permittivity of free space, 0m is the free electron mass, 3d k is the differential volume
element in k
space and is given by 3 24d k k dk , a is the polarization vector of the light
vector, ( )cE k
represents the energy of the conduction band (CB) with wave vector k
,
( )vE k
represents the energy of valence band (VB) with wave vector k
, respectively.
( ) ( ) ( )c vE k E k k
denotes the k
dependent energy difference between the VB and CB
and ( )cvp k
is the optical transition matrix elements (OME) , e
f and h
f are the electron
and hole Fermi-Dirac distributions while )(L k
is the Lorentzian line-shape broadening
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function, 2 2[ / (2 )] / [( )( 2)) ( / ]k
and depends on the relaxation time ,
in .
Due to the intraband relaxation process such as the electron-electron scattering, electron-
phonon scattering, etc., broadening occurs in the gain spectrum of semiconductor lasers
[7, 8]. When the scattering relaxation is included, the delta function may he replaced by a
Lorentzian function with a line width :
2 2
/ (2 )
( ) ( /( ) ( )
( ) ( ) 2)c v
c v
E k E kE k E k
(7.2)
where 2 factor has been included such that the area under the function is properly
normalized:
( ) ( ) ( ) 1c v
E k E k d
For the three band energy model of Kane, effective optical energy gap for optical
transitions at wave vector k
, is expressed as
1/22 2
2( ) ( ) ( )c v g g
r
kk E k E k E E
m
in which gE is the band-gap energy, rm is the reduced mass and is given by
1 1 1
cr vm m m , cm the effective mass of the conduction band electron and vm the
effective mass of the heavy hole at the top of the valence band. The dispersion law of the
conduction electrons in III–V binary, ternary and quaternary materials in accordance with
the three band model of Kane is given by [9]
22
( )2 c
kE
m
(7.4)
in which ( ) ( 1)( 1) / ( 1)E E a E b E c E , 1/ , 1/ ( )g ga E b E , is the spin-
orbit splitting constant and 1/ ( 2 / 3)gc E .
The Fermi functions e
f and h
f are given by
1
1
( )) [1 exp{( ( ) ) / }]
( )) [1 exp{( ( )( )
(
/ }]
e
h
c c
vv
fc
fv
f
f
E k E k E kT
E k E k E kT
(7.5)
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Here, the electrons and holes are assumed in equilibrium as determined by the quasi-
Fermi levels fcE and fv
E , respectively.
fcE and fv
E are related to the densities of injected electrons and holes [10]. Using the
generalized Sommerfeld’s lemma [11] and equal electron and hole injection into the
active laser medium (i.e., n p )
3/2
2 1
1 12
2(3 ) ( ) ( )c
fc fc
mn M E N E
3/2
2 1
1 12
2(3 ) ( ) ( )v
fv fv
mp M E N E
where
3/2
1( ) [ ( )]fc fcM E E
1 1
1
( ) ( ,0) ( )s
fc fc
r
N E D r M E
22 1 2
2( , ) [2( ) (1 2 ) (2 )]
r Jr r
r J
fc
D r J kT rE
where / 2h , is the reduced Planck’s constant.
Next, using the expression for OME in accordance with the three band energy
model of Kane as derived in the previous chapter (section 3.4.1 Eq. (3.72)) and carrying
out the integration the final expression for optical gain is arrived at (for the case 0 )
22[ ( )( ) ( ) ( ( )) ]
hbulk g M N eg G E ff f f (7.8)
in which ( )ef and ( )h
f are Fermi functions which correspon to injected electron and
hole concentrations given by Eqs. (7.6) and (7.7), and the coefficient
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1/22
2
0
( ).
6 ( 2 ).
/ 3
grbulk
r g g
EmeG
nc E E
(7.9)
and
21/21/2 ' 2
' ' ' '
2 2 (( ) 1
8 ( ( (
)
) ) )()
g g g
M
g
E E Esf
E
(7.10)
21/21/2 ' 2
' ' ' '
2 2 (( ) 1
4 ( ( (
)
) ) )()
g g g
N
g
E E Etf
E
(7.11)
Fermi functions may also be approximated as
2 2 1
2 2 1
) [1 exp{ / 2 (( ) ) / ( ) / }]
) [1 exp{ / 2 ( ( ) ) / ( ) /( }]
(r c g g c fc
r v g g
e
h v fv
f
f
m m E E E E kT
m m E E E E kT
(7.12)
wherec
E and v
E are the energy at the bottom of conduction band and at the top of valence
band prior to carrier injection, respectively. The first term in the exponential represents
the effect of nonparabolicity while the second term represent shift of quasi Fermi level
due to carrier injection. It is apparent that because of the presence of squared term the
effect of nonparabolicity is dominant factor in estimating the Fermi functions which in
turn determines the gain in laser.
7.2.2. Formulation of the generalized optical gain for wide band gap semiconductor
in bulk state
For wide band gap materials (gE ) where nonparabolicity in the band structure is
less, the above formulation of optical gain can be transformed easily to the results of gain
for wide band gap materials having parabolic energy band. Under the assumption
of 0 , or ' 0 and 0s it leads to ( ) 0Mf and ( ) 1Nf . Therefore, it
follows that for wide band gap III-V compound semiconductors, where 0 , the optical
gain can be expressed as
22
[ ( )( ) ]) (hbulk bulk eg
g G E f f (7.13)
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Under the constraints (gE or
gE ) together with the condition
fcE and 1
fvE , the injected carrier statistics given in Eqs. (7.6) and (7.7) assume the
forms
1/2 3/2
15( ) ( )
4c fc fc
kTn N F F
(7.14)
1/2 3/2
15( ) ( )
4v fv fv
kTp N F F
(7.15)
where 3/222 2 / , /c c fc fcN m kT E kT , is the nonparabolicity factor and
0( )
tF x is
the one parameter Fermi-Dirac integral of order 0t which can be written as [12]
0
0
1
0 0
1( ) (1 exp( )) ,
( 1)
t
tF x y y x dy
t
1y
where ( ) is the complete Gamma function, or for all 0t analytically continued as a
complex contour integral around the negative axis. It may be noted that for 0 , Eqs.
(7.14) and (7.15) assume the forms
1/2 ( )c fc
n N F , 1/2 ( )v fv
p N F
and Fermi functions in (7.12) are reduced to
1
1
) [1 exp{ / ( ) ( ) / }]
) [1 exp{ / ( ) ( ) / }
(
](
r c g c fc
r vh v
e
g v f
f
f
m m E E E kT
m m E E E kT
(7.16)
Hence the final expression for optical gain can be simplified to
22 1
1
( ) [1 exp{ / ( ) ( ) / }]
[1 exp{ / ( ) (
[
) / }] ]
g r c g c fc
r v vg fv
g G E m m E E E kT
m m E E E kT
(7.17)
where 1/22 2
0/ 6( ) /r r gcG e n m E , which is in agreement with the well known
results for parabolic band [1, 2].
7.2.3. Formulation of the generalized optical gain for QW structure of narrow band
gap semiconductors
The gain in a quantum well laser may be written as
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2
2
0
22
,
( )2
[
ˆ. ( )
( )( ( ) ,) ( )] ( ) (( ) )
cvwell av
c
well t
no r z
e h vnn cn vn
d k a p k
E k E
eg
m cn d
f f Lk k E k E k
(7.18)
where 2
td k is the differential elemental area in k
space and is given by 2 2t t td k k dk , a
is the polarization vector of the light vector, ( )cnE k
represents the nth
subband energy of
the conduction band (CB) with wave vector k
, ( )vnE k
represents the nth
subband energy
of valence band (VB) with wave vector k
, respectively. ( ) ( ) ( )cn vn nE k E k k
denotes
the k
dependent energy difference between the VB and CB, e
f and h
f are the electron
and hole Fermi-Dirac distributions while )(L k
is the Lorentzian line-shape broadening
function. The k
dependent effective band gap
1/2
2 2 ( )( ) ( ) ( ) c
n cn vn g g
r
m Ek E k E k E E
m
where ( )E and the corresponding subband energy levels n
E in the conduction band are
given by Eqs. (4.4) and (4.5) in chapter 4. The Fermi functions e
f and h
f are given by
1
1
( )) [1 exp{( ( ) ) / }]
( )) [1 exp{( ( ) ) / }
(
( ]
e
h vn vn
cn cn fcn
fvn
f
f
E k E k E kT
E k E k E kT
Here, as before, the electrons and holes are assumed in equilibrium determined by the
quasi-Fermi levels fcnE and fvn
E , respectively.
fcnE and fvn
E are related to the densities of injected electrons and holes[10]. Using the
generalized Sommerfeld’s lemma [11]
max
2 2 221
( , ) ( , )z
z
n
c
D fcn z fcn z
n
mn M E n N E n
Since for equal electron and hole injection 2 2D Dn p
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max
2 2 221
( , ) ( , )z
z
n
vD fvn z fvn z
n
mp M E n N E n
where
2
2
2
( ( )2
) z
c z
fcn fcn
n
m dM E E
2 2
1
( , ) ( ,0) ( , )s
fcn z fcn z
r
N E n D r M E n
where fcn
E is the quasi Fermi energy in the presence of size quantization as measured
from the edge of the conduction band in the vertically upward direction. Inserting next
the expression for OME in accordance with the three band energy model of Kane as
derived in the previous chapter (section 4.4.1 Eq. (3.72) and carrying out the integration
the final expression for optical gain for a well grown in the z-direction is arrived at (for
the case 0 )
2 2( ) sin ( ) 4 [ ( ) ( )]cos ( )hwell M N
n
well eGg ff ff (7.22)
in which ( )e
f and ( )h
f are Fermi functions to be corresponding to injected electron and
hole concentrations and ( )M
f , ( )N
f are as defined earlier.
Then,
2
0
( )( )
(8 )( 2 / (3 ))
g
well
z r gd
e EG
Cn E
, (7.23)
Fermi functions may be also be approximated as
2 2 1
2 2 1
) [1 exp{ / 2 (( ) ) / (0) ( ) / }]
) [1 exp{ / 2 ( ( ) ) / (0) (
(
( ) / }]
r c n n cn fcn
r v n n fvn
e
h vn
f
f
m m E E kT
m m E E kT
(7.24)
wherecn
E and vn
E are the subband energy at the bottom of conduction band and at the top
of the valence band prior to carrier injection. The first term in the exponential represents
the effect of nonparabolicity while the second term represent shift of quasi Fermi level
131
due to carrier injection. It is apparent for the expressions that the effect of nonparabolicity
plays dominant role in estimating the Fermi functions which in turn determines the gain
in laser.
7.2.4. Formulation of the generalized optical gain for QW structure of wide band
gap semiconductors
Under the assumption of 0 or ' 0 and 0s it leads to
( ) 0M
f and ( ) 1N
f . Therefore, it follows that for wide band gap III-V compound
semiconductors, where 0 , the optical gain can be expressed as
2( ) 4 [s ( ) ( )]coh
z
wewel l
n
el lg G f f (7.25)
Under the constraints (gE or
gE ), the injected carrier statistics given in (7.20)
and (7.21) assume the forms
max
2 2 0 1(1 2 ) ( ) 2 ( )n
D c cn fcn fcn
n
n N E F kTF (7.26)
max
2 2 0 1(1 2 ) ( ) 2 ( )n
D v vn fvn fvn
n
p N E F kTF (7.27)
where 2
2 / ( ) , ( ) /c c fcn fc cnN m kT E E kT , is the nonparabolicity factor and
( )j fnF is the one parameter Fermi-Dirac integral of order j .
It may be noted that for 0 , Eqs. (7.26) and (7.27) assume the forms
max
2 2 0 ( )n
D c fcn
n
n N F ,max
2 2 0 ( )n
D v fvn
n
p N F
while Fermi function in (7.24) reduces to
1
1
) [1 exp{ / ( ) ( ) / }]
) [1 exp{ / ( ) ( ) ]
(
( / }
r c n cn fcn
r v nh n
e
vn fv
f
f
m m E E kT
m m E E kT
(7.28)
Hence the final expression for optical gain can be simplified to
2 1
1
1
( ) 4 cos [1 exp{ / ( ) ( ) / }]
[
[
1 exp{ / ( ) ( ) / }] ]vn
well r c n cn fcn
n
r v n fvn
g G m m E E kT
m m E E kT
(7.29)
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where 2
1 0( ) / (8 )z rG e Cd n , which is in agreement with the well known results
reported for parabolic band [13- 16].
7.2.5. Formulation of the generalized optical gain for QWR structure of narrow
band gap semiconductors
The gain in a quantum wire laser may be written as
2
2
0
2
,
4( )
[ ( ) ( )
ˆ. ( )
( ) ( ) , ) (] ( ) ( )
wire l
m no r x y
e h vmn
cvwire av
cmn cmn vmn
eg
m cn d ddk a p k
E k E k kf f E k E kL
(7.30)
where l
dk is the differential elemental width in k
space, a is the light polarization
vector, ( )cmnE k
represents the subband energy level of the conduction band (CB) with
wave vector k
, ( )vmnE k
represents the subband energy level of valence band (VB) with
wave vector k
having subband indices m and n. ( ) ( ) ( )cmn vmn mnE k E k k
denotes the
k
dependent energy difference between the VB and CB, e
f and h
f are the electron and
hole Fermi-Dirac distributions while )(L k
is the Lorentzian line-shape broadening
function. Again, the effective band gap can be written as
1/2
2 2 ( )( ) ( ) ( ) c
mn cmn vmn g g
r
m Ek E k E k E E
m
(7.31)
where ( )E and the corresponding subband energy levels mn
E in the conduction band are
given by Eqs. (5.4) and (5.5) in chapter 5. The Fermi functions e
f and h
f are given by
1
1
( )) [1 exp{( ( ) ) / }]
( )) [1 exp{(
(
( ) / }( ) ]
cmn cmn fcmn
f
e
h vmn vmn vmn
f
f
E k E k E kT
E k E k E kT
Here, as before, the electrons and holes are in equilibrium as determined by the quasi-
Fermi levels fcmnE and fvmnE , respectively. fcmnE and fvmnE are related to the densities of
133
injected electrons and holes [10] and may be expressed using the generalized
Sommerfeld’s lemma [11]
max max
1 3 3
1 1
2 2( , , ) ( , , )
y y
x y
n n
c
D fcmn x x fcmn z x
n n
mn M E n n N E n n
and
max max
1 3 3
1 1
2 2( , , ) ( , , )
y y
x y
n n
v
D fvmn x x fvmn z x
n n
mp M E n n N E n n
where
222
3
2
2)
2( ) (
yx
c
f
x c
cmn fcmn
y
nn
m dE
m dM E
3 3
1
( , , ) ( ,0) ( , , )s
fcmn x y fcmn x y
r
N E n n L r M E n n
where fcmnE is the quasi Fermi energy in presence of size quantization as measured from
the edge of the conduction band in the vertically upward direction. Inserting next the
expression for OME in accordance with the three band energy model of Kane as derived
in the previous chapter (section 4.4.1 Eq. (3.72) and carrying out the integration the final
expression for optical gain for QWR grown in the z-direction is arrived at ( for the case
0 )
2
2
2
2
( )sin 2cos ( )( )
([ ( ) ( )]
) (0)h
U V
w
w
ire
n
ire
e
mnm
f fg
Gf f
(7.35)
in which ( )e
f and ( )h
f are Fermi functions corresponding to the injected electron and
hole concentrations and ( )U
f , ( )V
f are defined as earlier.
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Then
1/22
016 2 / 3
g g
wire
r r g
E EeG
n m EWc
(7.36)
Fermi functions may also be approximated as
2 2 1
2 2 1
) [1 exp{ / 2 (( ) ) / (0) ( ) / }]
) [1 exp{ / 2 ( ( ) ) / (0) (( ) }]
(
/
e
h vmn
r c mn mn cmn fcmn
r v mn mn fvmn
f
f
m m E E kT
m m E E kT
(7.37)
wherecmn
E and vmn
E are the subband energy at the bottom of conduction band and at the
top of valence band prior to carrier injection. The first term in the exponential represents
the effect of nonparabolicity while the second term represent shift of quasi Fermi level
due to carrier injection.
7.2.6. Formulation of the generalized optical gain for QWR structure of wide band
gap semiconductors
Under the assumption of 0 , ' 0 and 0s it leads to
( ) 0U
f and ( ) 1V
f . Therefore, it follows that for wide band gap III-V compound
semiconductors, where 0 , the optical gain can be expressed as
2
22
2[
co( ) ( )]
s( )
( ) (0)hwire
m nmn
wireefg
Gf
(7.38)
For the case of materials having (gE or
gE ), the injected carrier statistics given
in Eqs. (7.33) and (7.34) assume the forms
max max
1 1 0 1/2 1/2
0
1(1 (3 / 2) ) ( ) (3 / 4) ( )
n m
D c fcmn fcmn
n m
n N b F kTFa
(7.39)
and
max max
1 1 0 1/2 1/2
0
1(1 (3 / 2) ) ( ) (3 / 4) ( )
n m
D v fvmn fvmn
n m
p N b F kTFa
(7.40)
where
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1
0 0
222
1 0
2
( , )
[1 ( , )]; ( , )[1 ( , )] ;
2 2 / ( ) , ( /
2 2
)c c fcmn fcmn
yx
c x c y
m n
a m n b m n m n
N m kT E
nn
m d m d
b kT
,
is the nonparabolicity factor and ( )j fnF is the one parameter Fermi-Dirac integral of
order j .
It may be noted that for 0 , Eqs. (7.39) and (7.40) assume the forms
max max
1 1 1/2 ( )n m
D c fcmn
n m
n N F ,max max
1 1 1/2 ( )n m
D v fvmn
n m
p N F
1
1
) [1 exp{ / ( ) ( ) / }]
) [1 exp{ / ( ) ( ) / }
(
( ]
r c mn cmn fcmne
h vmr v mn fn vmn
f
f
m m E E kT
m m E E kT
(7.41)
Hence the final expression for optical gain can be simplified to
1
2 2
2
2
1
2 cos( ) [1 exp{ / ( ) ( ) / }]
( ) (0)
[1 exp{ /
[
]( ) ( ) / }]
wire r c mn
vmn
cmn fcmn
n mmn
r v mn fvmn
Gg m m E E kT
m m E E kT
(7.42)
where
1/22
2
016
g
r r
E
Wc
eG
n m
, which is in agreement with the well known results for
parabolic band [17, 18] reported earlier.
7.2.7. Formulation of the generalized optical gain for QD structure of narrow band
gap semiconductors
The gain in a quantum dot laser may be written as
22
2,
0
8ˆ. ( , . )
4
( , , ) ( , , ) ( )
( ) (
1( )
[ ) , ) ( ) ( )( ) ( )] (
dot
m n
cvdot av
lr x y z
cmnl vmnl mnl
cmn ce h vm mn vmn n
ea p m n l
m n d d d
E m n l E m n l k k
E k E k k E k E k
gc
f f L
(7.43)
where x
d , yd ,z
d are the dimensions of the dot respectively in the x , y and z direction
and m , n , l are the respective indices for the quantized k
vector of the electron and
136
mnlk simply denotes the value of the wave vector corresponding to sublevel energy when
transition occurs.cmnl
E ,vmnl
E are the energy sublevels in the conduction and valence
band, respectively, a is the light polarization vector ande
f and h
f are the electron and
hole Fermi-Dirac distributions while )(L k
is the Lorentzian line-shape broadening
function. The effective band gap
1/2
2 2 ( )( , , ) ( , , ) ( , , ) c mnl
mnl cmnl vmnl g g
r
m Em n l E m n l E m n l E E
m
(7.44)
where ( )mnl
E and the corresponding subband energy levels mnl
E in the conduction band
are given by Eq. (6.4) in chapter 6. The Fermi functions e
f and h
f are given by
1
1
( , , )) [1 exp{( ( , , ) ) / }]
( , , )) [1 exp{( ( ,
(
( , ) ) / }]
e
h vmnl vmn
cmnl cmnl fcmnl
fvmnll
f
f
E m n l E m n l E kT
E m n l E m n l E kT
Here, as before, the electrons and holes are in equilibrium as determined by the quasi-
Fermi levels fcmnlE and fvmnlE , respectively. fcmnlE and fvmnlE are related to the densities of
injected electrons and holes [10] and expressed using the generalized Sommerfeld’s
lemma [11] as
max max max
0 1
1 1 1
2( )
y y z
x y z
n n n
D fcmnl
n n nx y zd d
Fd
n
and
max max max
0 1
1 1 1
2( )
y y z
x y z
n n n
D fvmnl
n n nx y zd dF
dp
where ( ) /fcmn fcmnl cmnlE E kT
22 22 2 2
2)
2 2(
yx z
c x c y
fcmn
c z
nn n
m d m dE
m d
137
and fcmnl
E is the quasi Fermi energy in presence of size quantization as measured from the
edge of the conduction band in the vertically upward direction. Inserting next the
expression for OME in accordance with the three band energy model of Kane as derived
in the previous chapter (section 4.4.1 Eq. (3.72) and carrying out the integration the final
expression for optical gain for a quantum dot is arrived at (for the case 0 )
2 2( ) ( )sin 2cos [( ) ( ) ( )]
hdot U mnl V mnl
n l
t
m
do eg f ffG f (7.48)
in which ( )e
f and ( )h
f are the Fermi functions corresponding to injected electron and
hole concentrations and ( )U
f , ( )V
f are as defined earlier. Then
1/22
08 2 / 3
g g
x y z r r g
dot
E EeG
d d n mcd E
, (7.49)
Fermi functions may be also be approximated as
2 2 1
2 2 1
) [1 exp{ / 2 (( ) ) / (0) ( ) / }]
) [1 exp{ / 2 ( ( ) ) / (0) ( ) ]
(
}( /
r c mnl cme mnl nl fcmnl
r v mnl mnh l v n fvmm l nl
f
f
m m E E kT
m m E E kT
(7.50)
wherecmn
E and vmn
E are the subband energy at the bottom of conduction band and at the
top of valence band prior to carrier injection. The first term in the exponential represents
the effect of nonparabolicity while the second term represent shift of quasi Fermi level
due to carrier injection.
7.2.8. Formulation of the generalized optical gain for QD structure of wide band gap
semiconductors
Under the assumption of 0 , ' 0 and 0s it leads to
( ) 0U
f and ( ) 1V
f . Therefore, it follows that for wide band gap III-V compound
semiconductors, where 0 , the optical gain can be expressed as
22( ) [ ( ) (cos )]hdot
m n l
dot eg G f f (7.51)
Also for the materials satisfying the condition (gE or
gE ), the injected carrier
statistics given in (7.46) and (7.47) assume the forms
138
max max max
0 1
1 1 1
2( )
y y z
x y z
n n n
D fcmnl
n n nx y zd dF
dn
(7.52)
and
max max max
0 1
1 1 1
2( )
y y z
x y z
n n n
D fvmnl
n n nx y zd dF
dp
(7.53)
where
22 22 2 2
2 2 2(1 )
( ) /
yx z
c x c
fcmnl fcmnl
fcmnl fcmnl cmnl
y c z
nn n
m d m d mE E
E E kT
d
(7.54)
is the nonparabolicity factor and ( )j fnF is the one parameter Fermi-Dirac integral of
order j .
It may be noted that for 0 , Eqn. (7.50) assumes the form
1
1
) [1 exp{ / ( ) ( ) / }]
) [1 exp{ / ( ) ( )( ]
(
/ }
r c mnl cmnl fcmnl
r v mnl fvm
e
h v nl nlm
f
f
m m E E kT
m m E E kT
(7.55)
Hence the final expression for optical gain can be simplified to
2 1
1
3( ) cos [1 exp{ /2 ( ) ( ) / }]
[1 exp{ / ( ) (
[
/ ]) }]
dot r c mnl cmnl fcmnl
m n l
r v mn vml fnl vmnl
g m m E E kT
m m E
G
E kT
(7.56)
where
1/22
3
08
g
x y z r r
EeG
d d d nc m
, which is in agreement with the well known
results for parabolic band [19, 20] found in the literature.
These results thus obtained are applied to a number of III-V compound
semiconductors and their alloys having nonparabolic energy band and the effect of
nonrabolicity on gain has been estimated numerically.
7.3. Results and discussions
Using Eqs. (7.8) and (7.13) together with parameters as given in Table 1, the optical
gain spectra at T=300 K have been plotted in Figure 7.1, for InAs as function of carrier
139
density (in cm-3
) and photon energy (in eV) where the solid curve represents the
three-band model of Kane and the dashed curve exhibits the same dependence for
isotropic parabolic band. The curves are labeled as a, b and c for carrier
concentrations 18 31.5 10 cm , 18 32 10 cm
and 18 32.5 10 cm , respectively. Figures 7.2,
7.3 and 7.4 are the plots using parameters of Table 1 for all the cases of Figure 7.1 for
InSb, Hg1-xCdxTe and In1-xGaxAsyP1-y lattice matched to InP, respectively. A noticeable
difference between the results of the two models is seen from Figures 7.1-7.4. The gain
spectrum calculated with the parabolic band model is rather wide and its maximum is
shifted towards the higher photon energies, for all the materials. Such a behavior is due to
the larger energy difference between the quasi-Fermi levels resulting from the parabolic
band approximation. The nonparabolicity of the conduction band leads to a smaller quasi-
Fermi level for electrons, hence, the crossover between gain and absorption takes place at
lower photon energies.
It appears from Figure 7.1 that the peak gain values increases with the increase in
carrier densities for both three band model of Kane as well as the parabolic band. With
increase of density, the peak gain values for three band model of Kane become larger
than those for parabolic bands because of the larger reduced density of states available
due to nonparabolicity of band structure. From Figures 7.1 and 7.2, it appears that the
separation between the peak gain value for a given carrier density (say, 18 32 10 cm ), in
accordance with the two models is wider for InSb as compared with that of InAs. From
Figures 7.3 and 7.4 it is observed that the separation is greatest for Hg1-xCdxTe and least
for In1-xGaxAsyP1-y lattice matched to InP. The effect is more prominent in case of
materials having lower band gap and higher spin-splitting factor. Hg1-xCdxTe is one
classic example of this whereas In1-xGaxAsyP1-y lattice matched to InP having just the
opposite band structure characteristics shows negligible effect. The results of Figures 7.1
to 7.4 also show that the carrier density dependence of the emission wave length is
significantly different for three band model in comparison to parabolic band model and
the difference is more for the materials having narrow band gap. Thus the effective band
structure model of the relevant materials plays critical role in determining gain of diode
lasers.
140
In Figures 7.5-7.8 the gain spectrum of QW of the same materials for both three band
model of Kane and the parabolic band approximations are plotted at T=300 K and for
carrier densitiy 18 33.0 10 cm . Similar dependence is observed for QWR and QD of
various materials and are plotted in Figures 7.9-7.12 and in Figures 7.13-7.16,
respectively, at same temperature and the carrier density (i.e., at T=300 K and for carrier
densities 18 33.0 10 cm ). It is found that the separation between the peak gain value for a
given carrier density ( 18 33.0 10 cm ) is greatest for Hg1-xCdxTe and least for In1-
xGaxAsyP1-y lattice matched to InP for all low dimensional cases. Moreover, the peak gain
values increases with the three band model of Kane compared to the parabolic band
approximation as the band gap decreases due to the increasing effect of nonparabolicity
and valence band coupling for all cases of low dimensional structures. It is noted that for
all cases of low dimensions the gain spectrum calculated with the parabolic band model is
rather wide and its maximum is shifted towards the higher photon energies, for all the
materials. Such a behavior is due to the larger energy difference between the quasi-Fermi
levels resulting from the parabolic band approximation. The nonparabolicity of the
conduction band leads to a smaller quasi-Fermi level for electrons, hence, the crossover
between gain and absorption takes place at lower photon energies for low dimensions as
well as the bulk state.
For a relative assessment the gain spectrum for bulk as well as the low
dimensional cases of the individual materials taking into effect of nonparabolicity is
plotted as a function of the photon energies in Figures 7.17-7.20 at same temperature and
carrier density as earlier. From these figures it can be concluded that the peak gain value
increases with the decrease in band gap due to increasing effect of nonparabolicity and
valence band mixing in these low band gap materials. From Figures 7.17-7.20 it is
observed that the peak gain is greatest for Hg1-xCdxTe and least for In1-xGaxAsyP1-y lattice
matched to InP. The effect is more prominent in case of materials having lower band gap
and higher spin-splitting factor. Hg1-xCdxTe satisfies both of these conditions well
whereas In1-xGaxAsyP1-y lattice matched to InP having just the opposite band structure
characteristics shows negligible effect.
The generalized formulation developed here for all low dimensions can be utilized
effectively for the determination of optical gain of all types of diode lasers of III –V
141
compound semiconductors and their ternary and quaternary alloys. Besides this, the
influence of energy band models and the various band parameters on the optical gain of
these materials are also studied. The numerical results presented in this paper would be
different for other lasing materials but the nature of variation should be same. The
theoretical results developed here can be extended in analysing various related
parameters such as threshold current density, line width, lasing frequency and others.
7.4 Conclusion
In this chapter, simplified theory of optical gain in nonparabolic semiconductor laser
is developed considering the wave vector dependence of OME in accordance with the
three energy band model of Kane. Effect of nonparabolicity in the band structure, which
is the characteristics of such lower band gap materials, on gain using this model is
demonstrated. The effect of nonparabolicity being the dominant factor in the estimation
of Fermi function, it is rigorously taken into account in calculating laser gain of narrow
band gap semiconductors. Under certain limiting conditions, the well known results for
wide gap materials having parabolic energy bands are obtained as a special case of the
present analysis indicating the validity of the model. The results show a significant
deviation to the gain spectrum for lasers of narrow-gap materials having three band
model in comparison with the parabolic band model approximations. Moreover, carrier
density dependence on both the peak gain and the emission wavelength is also observed.
However, for relatively wide band gap materials the deviation of optical gain differs little
even if three band model is used instead of parabolic band model. Thus, inclusion of the
band nonparabolicity is necessary in modeling of laser diodes made of narrow-gap
materials. It may finally be noted that the purpose of the present chapter is not solely to
demonstrate the effect of nonparabolicity in optical gain but to formulate it in its most
generalized form.
142
Figure 7.1. Gain spectra in InAs at T=300 K for carrier densities: (a)18 31.5 10 cm
,
(b)18 32 10 cm
, and (c)18 32.5 10 cm
in accordance with three band model of Kane.
The dashed curves result from parabolic band.
Figure 7.2. Gain spectra in InSb at T=300 K for carrier densities: (a)18 31.5 10 cm
,
(b)18 32 10 cm
, and (c)18 32.5 10 cm
in accordance with three band model of Kane.
The dashed curves result from parabolic band.
143
Figure 7.3. Gain spectra in Hg1-xCdxTe at T=300 K for carrier densities: (a)18 31.5 10 cm
,
(b)18 32 10 cm
, and (c)18 32.5 10 cm
in accordance with three band model of Kane.
The dashed curves result from parabolic band.
Figure 7.4. Gain spectra in In1-xGaxAsyP1-y lattice matched to InP at T=300 K for carrier
densities: (a)18 31.5 10 cm
, (b)18 32 10 cm
, and (c)18 32.5 10 cm
in accordance with
three band model of Kane. The dashed curves result from parabolic band.
144
Figure 7.5. Gain spectra of QW in Hg1-xCdxTe at T=300 K for carrier densitiy18 33.0 10 cm
in
accordance with three band model of Kane. The dashed curve results from parabolic band.
Figure 7.6. Gain spectra of QW in InSb at T=300 K for carrier densitiy 18 33.0 10 cm
in
accordance with three band model of Kane. The dashed curve results from parabolic band.
145
Figure 7.7. Gain spectra QW in InAs at T=300 K for carrier densitiy 18 33.0 10 cm
in
accordance with three band model of Kane. The dashed curve results from parabolic band.
Figure 7.8. Gain spectra of QW in In1-xGaxAsyP1-y lattice matched to InP at T=300 K for carrier
densitiy 18 33.0 10 cm
in accordance with three band model of Kane. The dashed curve
results from parabolic band.
146
Figure 7.9. Gain spectra of QWR in Hg1-xCdxTe at T=300 K for carrier densitiy 18 33.0 10 cm
in
accordance with three band model of Kane. The dashed curve results from parabolic band.
Figure 7.10. Gain spectra of QWR in InSb at T=300 K for carrier densitiy 18 33.0 10 cm
in
accordance with three band model of Kane. The dashed curve results from parabolic band.
147
Figure 7.11. Gain spectra of QWR in InAs at T=300 K for carrier densitiy 18 33.0 10 cm
in
accordance with three band model of Kane. The dashed curve results from parabolic band.
Figure 7.12. Gain spectra of QWR in In1-xGaxAsyP1-y lattice matched to InP at T=300 K for
carrier densitiy 18 33.0 10 cm
in accordance with three band model of Kane. The dashed
curve results from parabolic band.
148
Figure 7.13. Gain spectra of QD in Hg1-xCdxTe at T=300 K for carrier densitiy 18 33.0 10 cm
in
accordance with three band model of Kane. The dashed curve results from parabolic band.
Figure 7.14. Gain spectra of QD in InSb at T=300 K for carrier densitiy 18 33.0 10 cm
in
accordance with three band model of Kane. The dashed curve results from parabolic band.
149
Figure 7.15. Gain spectra of QD in InAs at T=300 K for carrier densitiy 18 33.0 10 cm
in
accordance with three band model of Kane. The dashed curve results from parabolic band.
Figure 7.16. Gain spectra of QD in In1-xGaxAsyP1-y lattice matched to InP at T=300 K for carrier
densitiy 18 33.0 10 cm
in accordance with three band model of Kane. The dashed curve
results from parabolic band.
150
Figure 7.17. Comparative assessment of theoretical optical gain spectra of low-dimensional
quantum structures of Hg1-xCdxTe.
Figure 7.18. Comparative assessment of theoretical optical gain spectra of low-dimensional
quantum structures of InSb.
151
Figure 7.19. Comparative assessment of theoretical optical gain spectra of low-dimensional
quantum structures of InAs.
Figure 7.20. Comparative assessment of theoretical optical gain spectra of low-dimensional
quantum structures of In1-xGaxAsyP1-y lattice matched to InP.
152
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