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physica status solidi (b)

Femtosecond degenerate four‐wave mixing study of exciton coherence in wide‐gap II–VI quantum wells

T. Häpl, H. Nickolaus, F. Henneberger, Axel Schülzgen

Published Mar 1, 1996• 39 citations
Publisher

Abstract

Abstract This paper studies coherent excitons in the presence of alloy disorder by femtosecond degenerate four‐wave mixing on ternary (ZnCd)Se/ZnSe quantum wells. The use of very low excitation densities enables to uncover an impurity‐mediated exciton dephasing time of (16 ± 2) ps and a related homogeneous exciton width of only 80 μeV. At higher densities, the coherence loss speeds up dramatically due to exciton‐exciton interaction. Separating the contributions from inhomogeneous (photon echo) and homogeneous broadening to the spectrally resolved decay transients allows to deduce the energy dependence of the dephasing time across the disorder broadened exciton ensemble. Further, pronounced biexciton resonances are observed in the signal spectrum which exhibit characteristic polarization properties. For cross‐polarized pulses, the biexciton signal shows a striking stimulation when the excitation density is increased.

DOI
10.1002/pssb.2221940121

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Femtosecond coherent fields induced by many-particle correlations in transient four-wave mixing

W. Schäfer, D. S. Kim, Jagdeep Shah +5 more

We present a unified microscopic approach to four-wave mixing (FWM) in semiconductors on an ultrashort time scale. The theory is valid for resonant excitation in the vicinity of the excitonic resonance and at low densities. The most important many-particle effects, i.e., static and dynamical exciton-exciton interaction as well as biexcitonic effects are incorporated. The internal fields resulting from these interaction processes give rise to pronounced many-particle effects in FWM signals. Our results explain the dependence of FWM signals on the polarization geometry, especially if biexcitons contribute. Time-resolved (TR) FWM experiments show that the diffraction of the interaction induced fields dominate the FWM signals completely. This dominance of the interaction induced field at low temperatures is true regardless of density, detuning, or polarization geometry. While spectrally resolved FWM (-FWM) shows biexcitonic or bound excitonic contributions under various experimental conditions, TR-FWM is always completely delayed, peaking roughly at the dephasing time after both beams passed through. \textcopyright{} 1996 The American Physical Society.

Physical review. B, Condensed matter•Jun 15, 1996•105 citations
Abstract This paper studies coherent excitons in the presence of alloy disorder by femtosecond degenerate four‐wave mixing on ternary (ZnCd)Se/ZnSe quantum wells. The use of very low excitation densities enables to uncover an impurity‐mediated exciton dephasing time of (16 ± 2) ps and a related homogeneous exciton width of only 80 μeV. At higher densities, the coherence loss speeds up dramatically due to exciton‐exciton interaction. Separating the contributions from inhomogeneous (photon echo) and homogeneous broadening to the spectrally resolved decay transients allows to deduce the energy dependence of the dephasing time across the disorder broadened exciton ensemble. Further, pronounced biexciton resonances are observed in the signal spectrum which exhibit characteristic polarization properties. For cross‐polarized pulses, the biexciton signal shows a striking stimulation when the excitation density is increased.
We present a comparative study of time-integrated four-wave-mixing and femtosecond emission under resonant excitation on excitons in weakly disordered GaAs quantum wells. At highest exciton densities when dephasing dominates the spectral width (homogeneous broadening), we find that the rise time of the incoherent luminescence signal is given by TIii 2/2. At lowest densities, optical coherence times approach the exciton radiative lifetime (15 to 20 ps). This confirms our previous result that coherent resonant Rayleigh scattering is responsible for the short rise time of the excitonic emission. We also show clear evidence for dephasing due to exciton–phonon interaction, as the rise time of the emission decreases dramatically when the sample temperature is increased.
We have performed time-integrated as well as time-resolved femtosecond degenerate four-wave-mixing measurements on inhomogeneously broadened (Zn,Cd)Se/ZnSe quantum-well structures. Potential fluctuations due to alloy disorder in the ternary wells give rise to localized quasi-zero-dimensional excitons and biexcitons. For time-integrated detection, they manifest themselves by distinct (disorder-renormalized) quantum beats. Time resolving these transients reveals a free-induction-decay-like emission nature of the biexciton in contrast to the photon-echo exciton contribution. Using a five-level scheme, containing both biexcitons and antibound two-exciton states, this striking emission-type change is explained by fluctuation and correlation effects upon the biexciton binding energy. A combination of time-resolved and time-integrated four-wave mixing is thus a powerful tool to gain information about the disorder in a given kind of quantum structure.
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.
A picosecond time-resolved four-wave mixing technique is used to study the dephasing of nonlinear optical resonances in CdSe. At low temperature strong coherent, nonlinear signals at the free exciton resonance, at the biexciton resonance, and at the exciton-biexciton transition are observed. The observed correlation traces, i.e. the diffracted intensity versus the delay between the interfering light pulses, yield information on the dephasing process. Dephasing times for excitons as long as 40 ps, decreasing with increasing excitation density and temperature, are observed. A two-level model is applied to describe theoretically the dynamical behavior of the resonances, and to extract their homogeneous broadening, as well as their inhomogeneous broadening.
Spectrally resolved and time-integrated degenerate four-wave mixing (FWM) experiments with ultra-short pulses have been used to investigate the relaxation times and coherent interactions of excitons in the Boltzmann and in the quantum kinetic regime in ZnSe single quantum wells.Three-pulse FWM experiments using 100 fs pulses in a 10 nm thick ZnSe/ZnMgSe single quantum well reveal nearly equal zero-density dephasing rates for coherences between + σ and - σ heavy-and/or light-hole exciton states as compared to the dephasing rate of the interband coherence between these states and the ground state.The measurements also demonstrate that exciton-exciton scattering destroys the phase coherence between heavy-and light-hole excitons about three times more effectively than the coherence between + σ and + σ heavy-hole excitons.The different coherent nonlinear signals obtained in a three-beam FWM experiment are explained and reproduced by numerical calculations of the optical Bloch equations for a ten-level model including excitation induced dephasing (EID).Two-beam FWM experiments using 30 fs pulses on a 10 nm ZnSe quantum well reveal marked quantum beats and a pronounced non-exponential decay for delay times smaller ~500 fs.The pronounced peak at pulse overlap is attributed to rapid destructive interference of the created polarization and to spin dependent quantum kinetic effects caused by the transient formation of an electron-hole (eh) pair grating.The three-beam FWM trace shows a bi-exponential decay which is attributed to a nonlinear polarization that is caused by the interaction of polarization 3 k with both an exciton grating and an eh-pair grating.Model calculations using the OBEs of a two level system that includes ∑ -+
We present a unified microscopic approach to four-wave mixing (FWM) in semiconductors on an ultrashort time scale. The theory is valid for resonant excitation in the vicinity of the excitonic resonance and at low densities. The most important many-particle effects, i.e., static and dynamical exciton-exciton interaction as well as biexcitonic effects are incorporated. The internal fields resulting from these interaction processes give rise to pronounced many-particle effects in FWM signals. Our results explain the dependence of FWM signals on the polarization geometry, especially if biexcitons contribute. Time-resolved (TR) FWM experiments show that the diffraction of the interaction induced fields dominate the FWM signals completely. This dominance of the interaction induced field at low temperatures is true regardless of density, detuning, or polarization geometry. While spectrally resolved FWM (-FWM) shows biexcitonic or bound excitonic contributions under various experimental conditions, TR-FWM is always completely delayed, peaking roughly at the dephasing time after both beams passed through. \textcopyright{} 1996 The American Physical Society.