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Intensity-dependent absorption coefficient and refractive
index near the band gap of highly excited
semiconductors
Nguyen Ba An
To cite this version:
1
LE
JOURNAL
DE
PHYSIQUE
Short Communication
Intensity-dependent absorption
coefficient and
refractive
index
nearthe band
gap
of
highly
excited
semiconductors
Nguyen
Ba AnCentre for Theoretical
Physics, Academy
of Sciences ofVietnam,
Nghia
Do,
TuLiem,
HaNoi,
Viet-nam
(Reçu
le10 juillet
1989,accepté
le 25 octobre1989)
Résumé. - Nous étudions la
dépendance
du coefficientd’absorption
03B1 et de l’indice de réfraction nen fonction de l’intensité de lumière incidente au
voisinage
de la résonanceexcitonique.
Lecomporte-ment
non-bosonique
des excitons peut constituer un mécanisme de non-linéaritéoptique
conduisant à des formes bistables de 03B1 et n au-dessus de cette résonance.Abstract. 2014 The
dependence
ofabsorption
coefficient 03B1 and refractive index n on theintensity
of incidentlight
are studied near the exciton resonance. The non-boson behaviour of excitons may serve as a mechanismof optical nonlinearity leading
to bistableshapes
of 03B1 and n above the resonance.1
Phys.
France 51(1990)
1-4 ler JANVIER1990,
Classification
Physics
Abstracts 71.35-78.20D-78.901Wo
important
branches of research ofoptical
properties
inhighly
laser-excitedsemiconduc-tors near the
absorption
edge
are the derivation’of thedependence
of the dielectric function Eon exciton
density.
[1, 2]
and the determination of the conditions for the occurrence ofdensity
bistability (DB) [3-5].
As theintensity
I of incidentpumping
laseris,
among otherquantities,
anexperimentally
controlableparameter,
it is reasonable and even necessary to have concreteopti-cal characteristics
dependent
directly
on I rather than on o-. The aim of this communication is tostudy
such adependence
which in a sense can be seen as abridge connecting
the two branches of research mentioned above. Similar task has been donerecently
in thespectral region
near thetwo-photon
biexciton resonance[6].
Let us start from an effective bosonic Hamiltonian of Hanamura
[7]
describing
asystem
of manyinteracting
excitonsplaced
under the action of anexternally
driven monochromatic classical2
laser field with
frequency w : (h
= c = 1being
usedhereafter)
where
Ek
(t)
the electric fieldstrength
of the radiation inside thecrystal,
at
the creationoperator
of an exciton with wave vector p and energywxp, V
thesample
volume,
d the matrix element ofdipole
moment, w =267r Ebr3 /3, U
=7r-1/2r-3/2@ À
=77r,-3
withEb and
rbeing
thebinding
energy and radius of an exciton. The dielectric function(£00
thebackground
dielectricconstant)
can be derived from the
knowledge
of theaveraged
(over
theeigenstate
ofH)
value of thepolar-ization
operator Pk
which within the Hartree-Fockapproximation
is of the form :Using (1)
to setup
theequations
of motion for ak anda+ k
which will then be solved in theframe-work of the Hartree-Fock
approximation
for astationary regime. Putting
the solutions of ak anda+ k
into(3)
and then(3)
into(2)
we obtain :where
IIcv
the interband matrix element of the wave-vectoroperator,
e and m the free electroncharge
and massand y
the exciton inversedephase
timebeing
phenomenologically
introduced. Theabsorption
coefficient a and the refractive index n of CdS obtained from(4)
areplotted
asfunctions of x = w
/
wX infigures
1 and2,
resp., for 0’ =0 ;
9 x1015
and 1.8 x1016
cm- 3 .
TheFig.l.
Fig.2.
Fig.1 - Absorption
coefficient as functions of x.used
parameters
for CdS are £00 =7.6,
WX = 2.5528eV, Eb
= 32.9meV, r
= 25.5 x10-8
cm, me= 0.205 m, mh = 1.348 m,
Eg
(band gap)
= 2.5857 eV andy-
1 = 7ps.
We see that thepeaks
of the curves areshifting
tohigher frequency
region
forincreasing
excitondensity.
This is dueto the blue shift of the exciton energy level which in turn is caused
by
the non-boson character of excitons(w
=267rE br3/3
is the contribution ofpurely
kinematical exciton-excitoninteractions ;
the
dynamical
ones vanish in the k - 0 limit used here. For details see[7]). As
a matter offact,
the excitons aregenerated
optically
and a must begoverned
by
theinput
laserintensity
I =IEI2
/T with
T = 1 -1 -
qi]
/
] l +
qi]
being
the transmition coefficient at thevacuum-crystal
boundary
surface.Thus, a
and n as functions of Idepend parametrically
on a. The(cr- I ) -relation
is followed from the balance condition in a
stationary
situation :where E2 = lm E and T the exciton life time
equal
to about 0.5 ns for CdS. AsT,
c2 and n are alldependent
on crequation (5)
becomes a verycomplicated
onestronly
nonlinear in u. Thedepen-dences of cr on I are
numerically
evaluated for CdS andrepresented
infigure
3 which show theFig.3 -
Excitondensity
as functions of I.occurrence of DB for x > 1.0024. The threshold
intensity
for the DB is of the order of about 40w/cm2 .
Figures
4 and 5display
a and n as functions of I for several values of x.According
tofigure
Fig.4.
Fig.5.
Fig.4 - Absorption
coefficient as functions of I.4
3 the behaviour of a and n is bistable for x >
1.0024,
too. Note that x > 1.0024 means(w - wx)
>
6.4 meV which is well smaller than
(Eg -
wx)
= Eb =
32.9 meV This makespossible experimental
measurements in the exciton resonance
spectral region.
Theoretical curves of CdS for theintensity
of reflected beamIr
=(1 -
T ) I
versus thepumping
intensity
I are drawn infigure
6 as apossible
reference for
experimentalists.
Fig.6 -
Reflectedintensity
vs. incidentintensity.
Acknowledgements
.The author thanks Academicians
Nguyen
Van Hieu and DaoVong
Duc for their constantsupports
in this direction of research.
References