Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

Laser Physics

Photon echoes in disordered semiconductor quantum wells

DuncanG Steel, Steven T. Cundiff

Published Jan 1, 2002• 3 citations
OpenAlex

Abstract

Photon echo spectroscopy provides an important tool for studying excitonic relaxation in disor- dered GaAs/AlGaAs quantum wells. In this paper, we review the application of this methodology to the study of excitons localized due to interface fluctuations, which result in inhomogeneous broadening of the spectrum and relaxation due to migration among localization sites. The temperature and energy dependence of the relax- ation rates indicate complex scattering mechanisms. The dependence of the photon echo signal on polarization of the incident pulses shows a dramatic change in the broadening and dephasing characteristics. This response is interpreted in terms of polarization selection of localized versus delocalized excitons. Mechanisms for the polarization dependence are discussed in terms of coupling between opposite spin excitons.

Related papers

Coherent transient spectroscopy of excitons in GaAs-AlGaAs quantum wells

Steven T. Cundiff, Duncan G. Steel

Coherent transient optical spectroscopy techniques provide a means of studying the relaxation of electronic excitations in solids. Using these techniques the authors examine the relaxation of excitons in GaAs-AlGaAs multiple quantum wells at low temperature. Localization of excitons due to interface disorder results in inhomogeneous broadening of the absorption spectrum and relaxation due to migration between localization sites. The temperature dependence and energy dependence of the relaxation indicate the presence of complex scattering mechanisms. The dependence of the optical response on the polarization of the incident excitation fields is shown to result in a dramatic change of the dephasing and broadening characteristics of the optical response. This response is interpreted in terms of the presence of both localized and delocalized excitons. Mechanisms for the polarization dependence are discussed.>

IEEE Journal of Quantum Electronics•Jan 1, 1992•26 citations

Stimulated Photon Echoes and Free Polarization Decay in GaAs Multiple Quantum Well Structures: Evidence for Localized and Delocalized Excitons

M. D. Webb, Steven T. Cundiff, Duncan G. Steel

Recent experimental and theoretical work suggests that excitons in GaAs/AlGaAs multiple quantum wells may be localized by disorder, or delocalized with Bloch-type wavefunctions1. At low temperature, localized excitons are expected to be characterized by spectral diffusion and by long optical coherence times, while delocalized excitons have short coherence times and exhibit spatial mobility2. The short optical coherence time associated with delocalized excitons results in a linear absorption profile that is primarily homogeneously broadened, while the disorder associated with localized excitons leads to an inhomogeneously broadened profile. In this work, we investigate the energy and phase relaxation of HH1 excitons in GaAs/AlGaAs MQW's at low temperature, and provide evidence that, dependent on the exciton density, both localized and delocalized excitons contribute to the nonlinear optical response.

International Conference on Ultrafast Phenomena•Jan 1, 1990•0 citations

Picosecond Nonlinear Optical Studies of Exciton Relaxation in Multiple Quantum Well Structures.

Michael D. Webb

This work presents new results of experimental studies of exciton relaxation in GaAs/AlGaAs multiple quantum well materials, using transient nonlinear laser spectroscopy techniques. In the low excitation regime, effective optical Bloch equations similar to the density matrix formalism of a two-level system describe the response. Solutions of these equations appropriate for three-pulse scattering studies are presented, along with a discussion of new experimental techniques used in this work. Non-ideal conditions present in the molecular beam epitaxy growth process introduce monolayer fluctuations in the quantum well thickness, leading to inhomogeneous broadening and exciton localization at sites of minimum energy. Localized excitons are separated in energy from extended, quasi-delocalized states by the mobility edge. Studies of localized exciton relaxation indicate that these excitons relax on a much slower timescale than delocalized excitons. The temperature dependence of the localized exciton relaxation rate shows that above 15K, the excitons are thermally activated to extended states above the mobility edge. Below 15K the excitons relax by phonon assisted migration between localization sites. For temperatures above 5K, and for exciton energies greater than 1 meV below line center, an extra dephasing mechanism characterizes the exciton relaxation. The inhomogeneous broadening of the exciton leads to the emission of stimulated photon echoes in the experimental geometry used in this work. The time-resolved emission demonstrates the stimulated photon echo nature at low excitation densities. At higher excitation densities, the decay dynamics is more complex. The time-resolved emission shows the presence of a stimulated photon echo and a free polarization decay. This unusual result suggests that both a homogeneous and an inhomogeneous exciton distribution comprise the exciton resonance. Exciton relaxation at low excitation densities represents the interaction of the exciton with the lattice. At higher excitation densities, exciton-exciton and exciton-free carrier interactions modify the relaxation rates. The dependence of the exciton relaxation rate on excitation density shows that many-body effects play an important role in the exciton physics. Free carrier interactions are more efficient at increasing the exciton relaxation rate; both types of interactions are more important in quantum well systems than in bulk materials.

•Jan 1, 1990•0 citations

Nonlinear Response of Localized Excitons: Effects of the Excitation-Induced Dephasing

Paola Borri, W. Langbein, D. Birkedal +2 more

The polarization dependence of the ultrafast nonlinear response of localized excitons in GaAs/AlGaAs quantum wells has been investigated by spectrally resolved, transient four-wave mixing. The role of the excitation-induced dephasing in the delay dependence of the signal is discussed in detail. In particular, we show experimentally that the excitation-induced dephasing gives rise to a photon echo in inhomogeneous systems. We develop a simple analytical model for the delay dependence of the signal, which enables us to deduce the dephasing time from the four-wave mixing decay.

physica status solidi (a)•Nov 1, 1997•8 citations

Photon Echo from Localized Excitons in Semiconductor Nanostructures

S. V. Poltavtsev, I. A. Yugova, Ilya A. Akimov +2 more

An overview on photon echo spectroscopy under resonant excitation of the exciton complexes in semiconductor nanostructures is presented. The use of four-wave-mixing technique with the pulsed excitation and heterodyne detection allowed us to measure the coherent response of the system with the picosecond time resolution. It is shown that, for resonant selective pulsed excitation of the localized exciton complexes, the coherent signal is represented by the photon echoes due to the inhomogeneous broadening of the optical transitions. In case of resonant excitation of the trions or donor-bound excitons, the Zeeman splitting of the resident electron ground state levels under the applied transverse magnetic field results in quantum beats of photon echo amplitude at the Larmor precession frequency. Application of magnetic field makes it possible to transfer coherently the optical excitation into the spin ensemble of the resident electrons and to observe a long-lived photon echo signal. The described technique can be used as a high-resolution spectroscopy of the energy splittings in the ground state of the system. Next, we consider the Rabi oscillations and their damping under excitation with intensive optical pulses for the excitons complexes with a different degree of localization. It is shown that damping of the echo signal with increase of the excitation pulse intensity is strongly manifested for excitons, while on trions and donor-bound excitons this effect is substantially weaker.

arXiv:1803.10651•Physics of the Solid State•Aug 1, 2018•28 citations

Optical dephasing and transient grating experiments on 2-D excitons in GaAs single quantum wells

A. Honold, Lothar Schultheis, J. Kühl +1 more

Optical transitions of 2-D excitons are believed to represent a typical model for inhomogeneous line broadening due to the well width fluctuations of the quantum wells.1 Because of the inhomogeneous broadening and its specified relaxation processes (relaxation of delocalized excitons to localized states), it is difficult to obtain information on the intrinsic relaxation times of delocalized excitons in such multiple-quantum-well structures.

Journal of the Optical Society of America B•Feb 1, 1987•0 citations
Photon echo spectroscopy provides an important tool for studying excitonic relaxation in disor- dered GaAs/AlGaAs quantum wells. In this paper, we review the application of this methodology to the study of excitons localized due to interface fluctuations, which result in inhomogeneous broadening of the spectrum and relaxation due to migration among localization sites. The temperature and energy dependence of the relax- ation rates indicate complex scattering mechanisms. The dependence of the photon echo signal on polarization of the incident pulses shows a dramatic change in the broadening and dephasing characteristics. This response is interpreted in terms of polarization selection of localized versus delocalized excitons. Mechanisms for the polarization dependence are discussed in terms of coupling between opposite spin excitons.
Coherent transient optical spectroscopy techniques provide a means of studying the relaxation of electronic excitations in solids. Using these techniques the authors examine the relaxation of excitons in GaAs-AlGaAs multiple quantum wells at low temperature. Localization of excitons due to interface disorder results in inhomogeneous broadening of the absorption spectrum and relaxation due to migration between localization sites. The temperature dependence and energy dependence of the relaxation indicate the presence of complex scattering mechanisms. The dependence of the optical response on the polarization of the incident excitation fields is shown to result in a dramatic change of the dephasing and broadening characteristics of the optical response. This response is interpreted in terms of the presence of both localized and delocalized excitons. Mechanisms for the polarization dependence are discussed.>
Recent experimental and theoretical work suggests that excitons in GaAs/AlGaAs multiple quantum wells may be localized by disorder, or delocalized with Bloch-type wavefunctions1. At low temperature, localized excitons are expected to be characterized by spectral diffusion and by long optical coherence times, while delocalized excitons have short coherence times and exhibit spatial mobility2. The short optical coherence time associated with delocalized excitons results in a linear absorption profile that is primarily homogeneously broadened, while the disorder associated with localized excitons leads to an inhomogeneously broadened profile. In this work, we investigate the energy and phase relaxation of HH1 excitons in GaAs/AlGaAs MQW's at low temperature, and provide evidence that, dependent on the exciton density, both localized and delocalized excitons contribute to the nonlinear optical response.
This work presents new results of experimental studies of exciton relaxation in GaAs/AlGaAs multiple quantum well materials, using transient nonlinear laser spectroscopy techniques. In the low excitation regime, effective optical Bloch equations similar to the density matrix formalism of a two-level system describe the response. Solutions of these equations appropriate for three-pulse scattering studies are presented, along with a discussion of new experimental techniques used in this work. Non-ideal conditions present in the molecular beam epitaxy growth process introduce monolayer fluctuations in the quantum well thickness, leading to inhomogeneous broadening and exciton localization at sites of minimum energy. Localized excitons are separated in energy from extended, quasi-delocalized states by the mobility edge. Studies of localized exciton relaxation indicate that these excitons relax on a much slower timescale than delocalized excitons. The temperature dependence of the localized exciton relaxation rate shows that above 15K, the excitons are thermally activated to extended states above the mobility edge. Below 15K the excitons relax by phonon assisted migration between localization sites. For temperatures above 5K, and for exciton energies greater than 1 meV below line center, an extra dephasing mechanism characterizes the exciton relaxation. The inhomogeneous broadening of the exciton leads to the emission of stimulated photon echoes in the experimental geometry used in this work. The time-resolved emission demonstrates the stimulated photon echo nature at low excitation densities. At higher excitation densities, the decay dynamics is more complex. The time-resolved emission shows the presence of a stimulated photon echo and a free polarization decay. This unusual result suggests that both a homogeneous and an inhomogeneous exciton distribution comprise the exciton resonance. Exciton relaxation at low excitation densities represents the interaction of the exciton with the lattice. At higher excitation densities, exciton-exciton and exciton-free carrier interactions modify the relaxation rates. The dependence of the exciton relaxation rate on excitation density shows that many-body effects play an important role in the exciton physics. Free carrier interactions are more efficient at increasing the exciton relaxation rate; both types of interactions are more important in quantum well systems than in bulk materials.
The polarization dependence of the ultrafast nonlinear response of localized excitons in GaAs/AlGaAs quantum wells has been investigated by spectrally resolved, transient four-wave mixing. The role of the excitation-induced dephasing in the delay dependence of the signal is discussed in detail. In particular, we show experimentally that the excitation-induced dephasing gives rise to a photon echo in inhomogeneous systems. We develop a simple analytical model for the delay dependence of the signal, which enables us to deduce the dephasing time from the four-wave mixing decay.
An overview on photon echo spectroscopy under resonant excitation of the exciton complexes in semiconductor nanostructures is presented. The use of four-wave-mixing technique with the pulsed excitation and heterodyne detection allowed us to measure the coherent response of the system with the picosecond time resolution. It is shown that, for resonant selective pulsed excitation of the localized exciton complexes, the coherent signal is represented by the photon echoes due to the inhomogeneous broadening of the optical transitions. In case of resonant excitation of the trions or donor-bound excitons, the Zeeman splitting of the resident electron ground state levels under the applied transverse magnetic field results in quantum beats of photon echo amplitude at the Larmor precession frequency. Application of magnetic field makes it possible to transfer coherently the optical excitation into the spin ensemble of the resident electrons and to observe a long-lived photon echo signal. The described technique can be used as a high-resolution spectroscopy of the energy splittings in the ground state of the system. Next, we consider the Rabi oscillations and their damping under excitation with intensive optical pulses for the excitons complexes with a different degree of localization. It is shown that damping of the echo signal with increase of the excitation pulse intensity is strongly manifested for excitons, while on trions and donor-bound excitons this effect is substantially weaker.