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Journal de Physique IV (Proceedings)

Coherent excitonic effects in quantum wells

Jagdeep Shah, D. S. KIM

Published Oct 1, 1993• 1 citation
Publisher

Abstract

Coherent transient spectroscopy of semiconductor nanostructures has become an active field of research in recent years. Most such experiments are analyzed in terms of a simple two-level model in which the effects of interaction and induced fields are ignored. We discuss two very different cases where inclusion of these generally-neglected effects leads to large and important modification in the temporal response of the system. In the first case, interactions between excitons strongly modify the temporal response of four-wave-mixing (FWM) signals from quantum wells. This is the temporal analog of well-known effects in the spectral domain, such as bleaching of the exciton absorption and bandgap renormalization. In the second case, the shape of a low-intensity pulse is severely distorted after transmission through a typical quantum well sample. Interferometric measurements show that reradiation of induced polarization is responsible for the distortion. The distortion depends strongly on the dephasing time and has important implications for all time-resolved measurements. 1.

DOI
10.1051/jp4:1993541

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Coherent transient spectroscopy of semiconductor nanostructures has become an active field of research in recent years. Most such experiments are analyzed in terms of a simple two-level model in which the effects of interaction and induced fields are ignored. We discuss two very different cases where inclusion of these generally-neglected effects leads to large and important modification in the temporal response of the system. In the first case, interactions between excitons strongly modify the temporal response of four-wave-mixing (FWM) signals from quantum wells. This is the temporal analog of well-known effects in the spectral domain, such as bleaching of the exciton absorption and bandgap renormalization. In the second case, the shape of a low-intensity pulse is severely distorted after transmission through a typical quantum well sample. Interferometric measurements show that reradiation of induced polarization is responsible for the distortion. The distortion depends strongly on the dephasing time and has important implications for all time-resolved measurements. 1.
The coherent response of excitons in semiconductor nanostructures measured in four-wave mixing (FWM) depends strongly on the inhomogeneous broadening of the exciton transition. We investigate GaAs/Al0.3Ga0.7As single quantum wells (SQW) and AlxGa1-xAs mixed crystals. Additional to the usual phase-space filling nonlinearity, excitation-induced dephasing (EID) and biexciton formation (BIF) are important. EID leads to a strong dependence of the signal on the angle between the linear input polarizations. We find that EID persists in inhomogeneous systems, showing that the mutual density-dependent dephasing rate difference between two subsystems within the inhomogeneous distribution is strongly dependent on their energy difference. BIF is strongly affecting the cross-linear polarized FWM response. The signal for positive delay is dominated by the transitions from the one-exciton state X to the two-exciton states. Here, the third-order polarization at X-XX is not at the same resonance as the first-order polarization at 0-X. Consequently, the rephasing of the microscopic third-order polarization to the macroscopic FWM photon echo is blurred by the non-perfect correlation of X and XX energies, leading to a fast and non-exponential signal decay in delay time. For inhomogeneous broadenings larger than the biexciton binding energy, we find an enhanced biexciton binding energy, and a quenching of the oscillator strength of the unbound biexciton.
Summary form only given.The coherent response of excitons in semiconductor nanostructures, as measured in four wave mixing (FWM) experiments, depends strongly on the inhomogeneous broadening of the exciton transition. We investigate GaAs-AlGaAs single quantum wells (SQW) of 4 nm to 25 nm well width. Two main mechanisms are found to be important. First, the excitation-induced dephasing FWM signal (EID), which leads to a strong dependence of the signal on the angle between the linear input polarizations. The presence of the EID in the mainly homogeneously broadened sample (25 nm) is shown by the beating between EID and two-photon coherence (TPC) at the exciton for negative delay and co-linear polarized excitation. It vanishes for cross-polarized excitation, thus excluding the importance of local-field effects.
Coherently controlled four-wave-mixing (FWM) measurements have turned out to be a very sensitive tool to investigate the microscopic origin of the nonlinear optical response of semiconductor quantum-well structures, in particular if excitons are excited [1-3]. The measured signal oscillates as a function of the phase difference of the two interferometric pulses and is modulated additionally by contributions that oscillate with integer multiples of the excitonic resonance frequency. The influence of these harmonics can be measured in background free directions, i.e., the first (FWM) or second (six-wave mixing, SWM) diffracted order in direction 2k2-k1 or 3k2-2k1, respectively. Their intensity is easily quantified by inspecting the corresponding Fourier transforms (FT). Here, we report on transient interferometric SWM measurements and the influence of biexcitons on the signal.
Time-resolved four-wave-mixing experiments are usually interpreted in terms of noninteracting two-level systems in order to obtain information on the polarization dephasing time T2{\mathit{T}}_{2}T2​. Recent experiments involving excitonic resonances in semiconductor quantum wells (including results presented in this paper) show striking qualitative deviations from this simple picture. In particular, an exponential tail is observed at low excitation for negative time delays. At high excitation, the four-wave-mixing signal is found to evolve into two distinct temporal maxima. We demonstrate that the microscopic origin of this time dependence can be understood in terms of coherent exciton-exciton interactions. We show in fact that this behavior is more general and should be seen in numerous dense media where strong nonlinear interactions of polarizations occur. In addition to presenting rigorous numerical results, we analyze two simple situations in which such interactions exist: dielectric media with local-field effects and the anharmonic oscillator. We derive analytical expressions for their time-dependent four-wave-mixing response and discuss the physical origin of these new nonlinear-optical effects.
Summary form only given. Optical interactions in semiconductor microcavities embedded with quantum wells enter a nonperturbative regime when the dipole coupling rate between the exciton and the cavity mode exceeds relevant decay rates. In this regime, coherent energy exchange between the exciton and the cavity mode, i.e. normal mode oscillation (NMO), takes place when the cavity mode is excited impulsively by a short laser pulse. Similar coherent oscillations have also been observed in transient four-wave mixing (FWM) responses. In this paper, we present experimental and theoretical studies on the nature of oscillations in these transient FWM responses. We show that, in contrast to earlier beliefs, oscillations in time-integrated transient FWM do not correspond to NMO of the exciton or photon populations. Theoretical studies further reveal that FWM arising from different physical mechanisms including band filling, excitation-induced dephasing, and renormalized electric fields is characterized by highly distinct coherent dynamics. Oscillations in transient FWM reflect interference between these coherent optical processes and can be used as a unique probe for exciton many-body interactions in the nonperturbative regime.