Excitations in spatially indirect transitions feature such as excitons in type-II heterostructures or charge-transfer excitations in molecular crystals feature a permanent dipole moment which influences the transition dipole moments commonly probed by optical spectroscopy. Epitaxially grown III-V quantum heterostructures featuring suitable band alignments are ideal model systems to study the interplay between the two. Selected topics discussed include the AC Stark effect and signatures of spatially indirect coherent biexciton states as well as the potential for coherent optical current injection dynamics.
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.
The nonlinear optical response of quantum well excitons excited by optical fields is analyzed by numerical solutions of the semiconductor Bloch equations. Differential absorption spectra are computed for resonant pumping at the exciton resonance and the dependence of the absorption changes on the polarization directions of the pump and probe pulses is investigated. Coherent biexcitonic many-body correlations are included in our approach up to third-order in the optical fields. Results are presented for spatially-direct type-I and spatiallyindirect type-II quantum well systems. Due to the spatial inhomogeneity, in type-II structures a finite coupling between excitons of opposite spins exists already on the Hartree-Fock level and contributes to the absorption changes for the case of opposite circularly polarized pump and probe pulses.
Semiconductors are amongst the most efficient active laser media as they yield extreme wall-plug efficiencies. Their broad gain bandwidth also promise short-pulse operation. Yet, intrinsic charge-carrier relaxation dynamics limit the feasible repetition rates beyond constraints of cavity design and heat removal. In lieu of studying an operation device we monitor the population dynamics, i.e., the initial buildup of gain after optical excitation as well as its recovery after a stimulated emission process using multiple pump-probe spectroscopy. The first optical pulse injects hot charge carriers that eventually build up spectral gain in the sample. The energies are chosen such to mimic typical electrical injection surplus energies. Subsequently, a second laser pulse tuned to the broad spectral region in which gain is observed is used to stimulate emission and thus eliminate the gain. Analysis of the absorption spectra after stimulated emission reveals gain recovery times in the picosecond regime.
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