Preservation of quantum coherence after exciton-exciton interaction in quantum wells
N. Garro,
1,2
S. P. Kennedy,
1
R. T. Phillips,
1
G. Aichmayr,
3,
* U. Ro
¨
ssler,
3,²
and L. Vin
˜
a
3
1
Cavendish Laboratory, Madingley Road, Cambridge CB3 0HE, United Kingdom
2
Institut de Cie `ncia dels Materials, Universitat de Vale `ncia, E-46071 Vale `ncia, Spain
3
Departamento Fı ´sica de Materiales, Universidad Auto ´noma Madrid, E-28049 Madrid, Spain
Received 14 October 2002; revised manuscript received 9 January 2003; published 17 March 2003
The dynamics of exciton-exciton interaction in quantum wells has been investigated by monitoring the
time-resolved resonant secondary emission that follows excitation with linearly and circularly polarized light.
Preservation of quantum beating in the cross-polarized emission demonstrates that spin relaxation can take
place, for some scattering channels, without total quantum coherence loss. Interexciton electron exchange is the
scattering mechanism that explains the persistence of the beating and, since it is sensitive to the fine structure
of excitons, the shift by in the phase of the beating observed in the experiment.
DOI: 10.1103/PhysRevB.67.1213XX PACS numbers: 78.47.+p, 71.70.Gm, 78.66.Fd
Optical properties of low-dimensional semiconductor sys-
tems and devices depend strongly on the excitation density
( n
X
). For n
X
below 3 10
11
cm
-2
and at low temperatures,
excitons are stable and dominate the optical response of
GaAs quantum wells QW’s near the absorption edge.
Within this regime of moderate excitation density ( n
X
10
9
cm
-2
) exciton-exciton scattering plays a major role in
the resonant response of QW’s and, as the dominating phase-
breaking mechanism, governs the dynamics of coherent tran-
sients. Since excitons confined in low-dimensional semicon-
ductor systems have been suggested as possible candidates
for quantum computation
1
it is important to understand the
mechanisms involved in the loss of optical coherence be-
tween the excitonic ensemble and the exciting light. The
study of exciton dephasing has been most often attempted by
means of nonlinear techniques.
2
Nevertheless, coherent fea-
tures are also present in the linear response of QW’s: the
resonant secondary nonspecular emission RSE has a co-
herent component resulting from scattering with static
disorder.
3
Thus time-resolved RSE can be used as a probe of
the coherence of the excitonic ensemble providing informa-
tion about scattering with dynamic disorder, such as exciton-
exciton scattering, that leads to exciton dephasing.
4,5
Recent
studies have shown that exciton-exciton interaction also con-
tributes to the depolarization of RSE due to exciton spin
relaxation.
6,7
The efficiency of such spin-relaxation channels
increases with increasing excitation ellipticity. In the limiting
case of linearly polarized excitation, the degree of polariza-
tion of RSE decays in a time scale comparable to typical
dephasing times for GaAs QW’s 10 ps and depends
strongly on n
X
. These experimental results are well ex-
plained in terms of interexciton exchange of carriers.
8,9
For
circularly polarized excitation, on the other hand, spin relax-
ation is a much slower density-independent process.
10,11
Periodic oscillations can appear in the time evolution of
RSE due to the simultaneous resonant excitation of more
than one excitonic transition. Beating between heavy-hole
hh and light-hole lh excitons has been observed in the
emission of wide QW’s.
12,13
The visibility of the beating de-
cays in a time scale of the order of 10 ps and depends on n
X
.
Determining the origin of the beating—whether it results
from the quantum nature of the superposition of states or
from classical interferences at the detector—is not trivial.
Distinguishing between these two possibilities required per-
forming a specific experiment in the case of beating observed
in time-resolved four-wave mixing.
14
So far there are no con-
clusive studies about the nature of the beating present in the
linear emission of QW’s.
In this Rapid Communication we address two important
issues regarding exciton coherence in QW’s: the nature of
hh-lh exciton beating in RSE and the effect of exciton-
exciton interaction as a coherence-breaking mechanism. We
studied the depolarization of time-resolved RSE from wide
QW transitions after excitation with linearly polarized light
in the density regime where exciton-exciton scattering is the
dominant spin-relaxation mechanism. The improved time
resolution of our experiment allowed the observation of sev-
eral features indicating that spin relaxation can take place
without coherence loss. We have identified the exciton-
exciton scattering mechanism responsible for such effects.
The experimental results presented in this Rapid Commu-
nication correspond to a single 15-nm GaAs QW with
Al
0.33
Ga
0.67
As barriers sample A ) and a multiple-QW struc-
ture containing ten repetitions of 20-nm GaAs wells sepa-
rated by GaAs/AlAs superlattice barriers sample B ). Both
samples showed narrow emission linewidths at low tempera-
tures, with full width at half maximum of 0.8 meV and 0.7
meV for samples A and B, respectively. We measured the
time evolution of the RSE by means of two-color up-
conversion spectroscopy for more details about the experi-
mental setup see Ref. 13. Excitation and gating pulses were
140-fs long 13-meV bandwidth, which kept the time reso-
lution below 200 fs, shorter than in previous studies.
6,7
Excitation of the sample was done in the backscattering ge-
ometry with the laser pulse propagating parallel to the
growth direction z of the sample. All measurements were
done at 6 K.
Time-resolved RSE spectra of sample A for identical n
X
but corresponding to different excitation and detection con-
ditions are plotted in Fig. 1. The excitation pulse was either
circularly polarized a or linearly polarized along the x di-
rection b and the detected emission was copolarized solid
lines and cross-polarized dashed lines with respect to the
excitation. Copolarized emission has an intense spike at t
RAPID COMMUNICATIONS
PHYSICAL REVIEW B 67, 121302R2003
0163-1829/2003/6712/1213024/$20.00 ©2003 The American Physical Society 67 121302-1