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Journal of the Optical Society of America B

Spectral signatures of χ^(5) processes in four-wave mixing of homogeneously broadened excitons

W. Langbein, T. Meier, S. W. Koch, J. M. Hvam

Published Sep 1, 2001• 44 citations
Publisher

Abstract

The influence of fifth-order coherences on the spectrally resolved four-wave mixing response of predominantly homogeneously broadened quasi-two-dimensional excitons is studied. Fifth-order signatures are discussed as a function of spectral position and excitation polarization. An exciton–biexciton beating for positive delay times is the dominant effect, which is pronounced at the exciton–biexciton transition for collinearly polarized excitation and at the exciton transition for cross-linearly polarized excitation. For negative delay times and collinearly polarized excitation a pronounced exciton–biexciton beating at the exciton resonance is observed that is vanishing for long negative delays owing to the faster dephasing in the two-exciton continuum compared with the bound biexciton state. These results are in qualitative agreement with microscopic model calculations that include the coherent dynamics of one- and two-exciton resonances up to the fifth order in the optical field.

DOI
10.1364/josab.18.001318

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The influence of fifth-order coherences on the spectrally resolved four-wave mixing response of predominantly homogeneously broadened quasi-two-dimensional excitons is studied. Fifth-order signatures are discussed as a function of spectral position and excitation polarization. An exciton–biexciton beating for positive delay times is the dominant effect, which is pronounced at the exciton–biexciton transition for collinearly polarized excitation and at the exciton transition for cross-linearly polarized excitation. For negative delay times and collinearly polarized excitation a pronounced exciton–biexciton beating at the exciton resonance is observed that is vanishing for long negative delays owing to the faster dephasing in the two-exciton continuum compared with the bound biexciton state. These results are in qualitative agreement with microscopic model calculations that include the coherent dynamics of one- and two-exciton resonances up to the fifth order in the optical field.
We investigate the four-wave mixing response of semiconductor quantum wells having a predominantly inhomogeneous broadening of the exciton states. The influence of the biexcitons on the nonlinear emission, in proximity to the lowest exciton resonance, is studied. Using about 1 ps long pulses, we show that biexcitons are created for all excitation energies lying within the broadened exciton absorption line, and that their binding energy does not depend on the exciton energy. Reducing the temporal width of cross-linearly polarized incident laser fields to about 0.1 ps, we observe a drastic changeover from a prompt response to a photon echo, and quite interesting beating phenomena, visible in time-integrated as well as in time-resolved experiments, appear. Our observations compare well with the numerical solutions of the optical Bloch equations for a five-level scheme. The influence of the inhomogeneous broadening on the beating phenomena is discussed.
The time-averaged polarization angles of excitonic and biexcitonic four-wave-mixing signals are investigated in spectrally resolved measurements for different angles between the linear excitation polarizations, delay times and pulse energies. For an angle close to 90° between the two incident polarizations the signal emitted at the spectral position of the excitonic resonance clearly shows different polarization angles as the delay is changed from negative to positive. Additionally, the polarization angles of the signals exhibit oscillations which are differently pronounced for negative and positive delay times. The experimental results are compared with numerical calculations based on a phenomenologically extended five-level model of the exciton-biexciton system.
Four-wave-mixing signals from excitons under linear-circular polarized excitation exhibit an elliptical polarization, depending on both the pulse delay and the spectral position. Besides the resonances corresponding to excitons and exciton-biexciton transitions, a breakup of the exciton line is found reflecting the influence of correlations on the four-point level. An analysis accounting for the exciton density, the bound biexciton, and the exciton-exciton scattering continuum reveals that these features are not due to an antibound two-exciton state. Instead, they result from an interference of the correlated exciton continuum with the exciton density. In addition, the modeling shows that the signals ellipticity is highly sensitive to the influences of different correlations and, therefore, allows for a discrimination of their contributions.
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.
We investigate the spectral properties of the excitonic nonlinear response in a GaAs quantum-well sample containing wells of different thicknesses. We observe both the heavy-hole biexciton and the light-hole biexciton in the transient four-wave mixing spectrum and estimate their binding energy dependence on well width. For moderate excitation densities the signal for negative delay at the heavy-hole exciton and biexciton resonances is due to two-photon transitions to the biexciton states through the exciton states. The temporal behavior of the transient four-wave mixing signal from the heavy-hole exciton resonance is strongly dependent on the spectral position of the laser. We show that this effect is due to interference phenomena and to excitation-induced dephasing.
The nonlinear optical response of quantum well excitons is investigated experimentally using polarization resolved four wave mixing, optical-pump optical-probe, and optical-pump Terahertz-probe spectroscopy. The four-wave mixing data reveal clear signatures of coherent biexcitons which concur with straight-forward polarization selection rules at the Γ point. The type-I samples show the well-established time-domain beating signatures in the transients as well as the corresponding spectral signatures clearly. The latter are also present in type-II samples; however, the smaller exciton and biexciton binding energies in these structures infer longer beating times which, in turn, are accompanied by faster dephasing of the type-II exciton coherences. Furthermore, the THz absorption following spectrally narrow, picosecond excitation at energies in the vicinity of the 1s exciton resonance are discussed. Here, the optical signatures yield the well-established redshifts and blueshifts for the appropriate polarization geometries in type-I quantum well samples also termed “AC Stark Effect”. The THz probe reveals intriguing spectral features which can be ascribed to coherent negative absorption following an excitation into a virtual state for an excitation below the 1s exciton resonance. Furthermore, the scattering and ionization of excitons is discussed for several excitation geometries yielding control rules for elastic and inelastic quasiparticle collisions.