In order to optimize opto-electronic applications of semiconductor nanostructures, a deep understanding of optical nonlinearities is essential.One fundamental method currently used within this field of research is ultrafast optical spectroscopy.This work presents a theoretical study of optical nonlinearities in semiconductor quantum wells in the coherent time regime.The theory is based on the equations of motion for the coherent exciton and biexciton transition amplitudes.These equations are derived using two different ways: Heisenberg equations of motion in combination with the dynamics-controlled truncation theory and alternatively the non-equilibrium Green´s function technique. For the coherent regime both approaches are equivalent and can be used to formulate a coupled set of equations for the coherent excitation dynamics that is correct up to the third order in the optical field.In contrast to the dynamics-controlled truncation theory the non-equilibrium Green´s function technique allows the inclusion of incoherent scattering processes into the description.The theory is evaluated to describe pump and probe as well as four-wave-mixing experiments with ZnSe quantum wells.Numerical calculations for the coherent control of the macroscopic polarization andthe dependence of transient four-wave-mixing on the light-polarization and intensity are both in good agreement with experiments.In order to correctly describe elevated excitation conditions for the latter investigation, the theory is self-consistently extended such that the included excitonic and biexcitonic nonlinearities contribute up to arbitrary order in the optical field.
In order to optimize opto-electronic applications of semiconductor nanostructures, a deep understanding of optical nonlinearities is essential.One fundamental method currently used within this field of research is ultrafast optical spectroscopy.This work presents a theoretical study of optical nonlinearities in semiconductor quantum wells in the coherent time regime.The theory is based on the equations of motion for the coherent exciton and biexciton transition amplitudes.These equations are derived using two different ways: Heisenberg equations of motion in combination with the dynamics-controlled truncation theory and alternatively the non-equilibrium Green´s function technique. For the coherent regime both approaches are equivalent and can be used to formulate a coupled set of equations for the coherent excitation dynamics that is correct up to the third order in the optical field.In contrast to the dynamics-controlled truncation theory the non-equilibrium Green´s function technique allows the inclusion of incoherent scattering processes into the description.The theory is evaluated to describe pump and probe as well as four-wave-mixing experiments with ZnSe quantum wells.Numerical calculations for the coherent control of the macroscopic polarization andthe dependence of transient four-wave-mixing on the light-polarization and intensity are both in good agreement with experiments.In order to correctly describe elevated excitation conditions for the latter investigation, the theory is self-consistently extended such that the included excitonic and biexcitonic nonlinearities contribute up to arbitrary order in the optical field.
This dissertation addresses both fundamental aspects of Coulomb correlations in semiconductor quantum wells and more practical aspects of theoretical analysis of semiconductor optoelectronic devices. After introducing the subject, we present and evaluate a state-of-the-art theory of the third order coherent optical response of a semiconductor quantum well based on the Dynamics Controlled Truncation (DCT) scheme. Already in the third order (the so-called chi (3)) regime, semiconductors exhibit a number of many-body Coulomb correlation effects. Their manifestation in various multi-pulse experimental configurations, customarily used in ultrafast semiconductor spectroscopy, has been an important component of this thesis. Coherent optical effects in a semiconductor 3-band system based on the heavy-hole, light-hole and conduction bands were investigated. The quantum beats in the time-integrated differential transmission signal were analyzed and compared with experimental data obtained at the University of Iowa. Fundamental differences from corresponding quantum beats in atomic 3-level systems were found. Also, the analysis of experimental data (obtained at the University of Arizona) of the coupled heavy-hole-light-hole optical Stark shift revealed evidence of intervalence band coherences, an analog of Raman coherences in atomic 3-levels systems. A scheme for realization of electromagnetically-induced transparency (EIT) based on the interference of excitonic and biexcitonic coherences was proposed. Corresponding experiments performed at the University of Oregon showed indeed a considerable coherent reduction of excitonic absorption. Furthermore, an extension of the chi(3) analysis revealed an energy renormalization of the biexciton, in good agreement with the corresponding experiment. A microscopic analysis of polarization dynamics in time-resolved four-wave mixing signals was performed, revealing interesting implications for the biexciton dephasing in addition to the significance of many-body correlations. In the case of four-wave mixing in semiconductor microcavities, our theoretical analysis in conjunction with experimental data obtained at the University of Tokyo gave us indications for a significant shortcoming of the second Born approximation (2nd BA) applied to two-exciton Coulomb correlations in a thin semiconductor quantum well, in agreement with the general knowledge of the qualitative failure of the 2nd BA in systems with short-range interaction in two dimensions. We also analyzed a novel all-optical switching technique based on the nonlinear polarization rotation. Apart from identifying the many-particle processes relevant for the switch operation in the chi(3) regime, we proposed ways to further optimize the switch.
The paper presents a description of two-pair correlations in an electron-hole system in laser-excited direct-gap semiconductors in terms of the exciton-boson formalism. The dependence of the states of quasi-particles on their angular momentum orientation is properly taken into account following group theory rules. It is shown for the example of heavy hole excitons in GaAs quantum wells that Coulomb two-exciton correlations include effective repulsion between excitons with nonzero total momenta and effective attraction between excitons with zero total momenta. They generate exciton and biexciton nonlinearities, respectively, in the exciton-biexciton system. The Heisenberg equations of motion derived are applied to four-wave mixing in the coherent mode. Two components of Coulomb two-exciton correlations were found to generate coherent four-wave mixing either separately, one at the cocircular and the other at the perpendicular-linear polarization of applied pulses, or jointly at parallel-linear polarization. General equations are obtained for the amplitude of four-wave mixing signals with time resolution in these polarization configurations, which, in the limit of ultranarrow pulses, reduce to analytic functions of time and excitation and sample parameters. These equations are used to analyze signal characteristics in every polarization configuration. The results give a correct picture of biexciton effects and the polarization dependence of coherent four-wave mixing in GaAs quantum wells.
A detailed numerical study of the third-order nonlinear optical susceptibilities (χ(3)) of semiconductor quantum wells is presented. The dependence of χ(3) on material parameters (electron-hole mass ratio and exciton linewidths), on the light polarization configuration (co- and countercircularly polarized) and on the spectral configuration is discussed. The goal of this study is to map out the nonlinear phase shift per quantum well and a related figure of merit caused by quasi-resonant excitonic and biexcitonic nonlinearities induced by picosecond light pulses. The study is based on the dynamics-controlled truncation formalism and evaluated under the assumption that only 1s-heavy-hole excitons contribute to the nonlinearities. It includes all correlation effects (exciton–exciton scattering in the singlet and triplet channels and coherent biexciton formation in the singlet channel) that contribute within the coherent excitonic χ(3) regime.
Summary form only given. The coherence decay of optically excited electronic systems provides one of the most powerful tools to investigate interaction processes of excited states. In semiconductors, the optical coherence phenomena are usually investigated by nonlinear techniques such as four wave mixing (FWM), photon echo, or reflectivity experiments. Exciton-phonon, exciton-exciton, or exciton-free carriers scattering processes have been explored in recent years with these techniques. As demonstrated recently, a direct measurement of the optical dephasing time can be obtained through the temporal coherent control of electronic excitations. In these experiments, the emission following the excitation by an ultrashort optical pulse sequence, is detected in a non-specular direction (secondary emission). This provides an alternative approach to FWM techniques, which allows us to analyse the scattering processes either with phonons or due to mutual collisions. Using the coherent control technique monitored through the secondary emission (SE), we report on the coherent dynamics of excitons in bare quantum wells (QW) and compare it to that of exciton-polaritons in microcavity (MC) embedded quantum wells.
By use of an optical coherent-control technique we demonstrate and analyze the control of transitions involved in the generation of four-wave-mixing signals in a semiconductor quantum well for the two different four-wave-mixing directions and for different sequences of the excitation pulses. Results are presented for frequency- as well as for time-resolved signals. A doubling of the coherent switching frequency is found which occurs if the laser pulses performing the control process contribute quadratically to the wave-mixing signal. A direct comparison between experiment and microscopic theory reveals how the coherent-control process acts on the coherent polarization of the exciton-biexciton system in all different configurations. An additional interpretation of the experimental results based on a simplified few-level model is able to provide an intuitive understanding of the relevant processes which govern the coherent control of the excitonic and biexcitonic wave-mixing polarizations.
Excitons, the bound states of an electron and a hole, in semiconductors are interesting
objects and they continue to attract attention of researchers from all over the world. Despite intense research on exciton physics over last three-four
decades, many interesting phenomena related to the dynamics and the nonlinear optical
properties of excitons in semiconductors and their nanostructures in the coherent and
incoherent regimes are still to be explored. This thesis presents our effort to study the
nonlinear optical properties as well as the exciton dynamics in coherent and incoherent
regime in semiconductor nanostructures including GaAs quantum wells (QWs) and InAs
quantum dots (QDs).
We have set up several time-resolved and steady-state optical spectroscopic measurement
techniques in our laboratory to carry out our study on excitons dynamics in
semiconductor QWs and QDs. We work out a clear and detailed theory of the pump-probe signal taking account of all aspect of the measurement, namely,
the lock-in detection, spectral selection by the monochromator and time-integration at
the slow photodetector. We have used the formalism of optical Bloch equations conventionally
used to analyse wave mixing experiments. Our analysis puts the pump-probe
technique on the same footing as the wave mixing experiments. We show that pumpprobe
experiments can be used to study both coherent and incoherent dynamics. We
also present a clear physical picture of the measured signal using the Lorentz harmonic
oscillator model.
We report the investigation of the coherent exciton dephasing dynamics using pumpprobe
reflectivity measurement in GaAs QWs for resonant excitation. Two GaAs/AlGaAs
QWs with well thicknesses 8 nm and 17.5 nm are used. We found a strong dependence of
the dephasing rate of the excitons with increasing exciton density due to exciton-exciton
scattering. We found that the exciton dephasing rate of 8 nm QWs at low excitation density
and at low lattice temperature is larger than the corresponding dephasing rate of the
17.5 nm QWs, possibly due to larger effect of inhomogeneous broadening. We also report
that the dephasing rates for both QWs are linear with the sample temperature below the
30 K.
We report the study of ionization equilibrium between the exciton and the electronhole
plasma population in the temperature and pressure (excitation density) phase space.
Non-resonant excitation of semiconductor creates a nonequilibrium state of electron-hole
plasma. We investigate this ionization equilibrium using steady state photoluminescence
and time-resolved excitation correlation PL measurements. We present a
clear phase diagram (in temperature and carrier density phase space) of this ionization process.A clear density-dependent increase in the ionization ratio is observed and its
connection with the Mott transition is discussed.
Semiconductor nanocrystals and QDs are another important area of research, mainly
due to their huge potential for device application. We present a simple
model which combines carrier loss kinetics, detailed balance principle in thermodynamic
equilibrium and Pauli exclusion principle to quantitatively explain the observed behaviour
of the experimental data.