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arXiv:cond-mat/0204463

Optically induced coherence effects in `artificial atoms and molecules'

Ulrich Hohenester, Filippo Troiani, Elisa Molinari

Published Apr 22, 2002• 1 citation
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Abstract

Using a master-equation approach for the description of coherent and incoherent dynamics in `artificial atoms and molecules', we present a theoretical analysis of situations where intense laser fields lead to pronounced renormalizations of carrier states. Such enhanced light-matter interactions allow for the solid-state implementation of effects hitherto only observable in atomic systems. Two prototypical examples will be presented: first, we show how two intense laser pulses can be exploited for a robust and high-fidelity population transfer of carrier states in coupled quantum dots; second, we discuss the possibility of observing self-induced transparency in a sample of inhomogenously broadened quantum dots, a phenomenon where intense laser pulses propagate without suffering significant losses.

DOI
10.48550/arxiv.cond-mat/0204463

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Using a master-equation approach for the description of coherent and incoherent dynamics in `artificial atoms and molecules', we present a theoretical analysis of situations where intense laser fields lead to pronounced renormalizations of carrier states. Such enhanced light-matter interactions allow for the solid-state implementation of effects hitherto only observable in atomic systems. Two prototypical examples will be presented: first, we show how two intense laser pulses can be exploited for a robust and high-fidelity population transfer of carrier states in coupled quantum dots; second, we discuss the possibility of observing self-induced transparency in a sample of inhomogenously broadened quantum dots, a phenomenon where intense laser pulses propagate without suffering significant losses.
Both coherent pumping and energy relaxation play important roles in understanding physical processes of ultra-intense coherent light-matter interactions. Here, using a large-scale quantum master equation approach, we describe dynamical processes of practical open quantum systems driven by both coherent and stochastic interactions. As examples, two typical cases of light-matter interactions are studied. First, we investigate coherent dynamics of inner-shell electrons of a neon gas irradiated by a high-intensity X-ray laser along with vast number of decaying channels. In these single-photon dominated processes, we find that, due to coherence-induced Rabi oscillations and power broadening effects, the photon absorptions of a neon gas can be suppressed resulting in differences in ionization processes and final ion-stage distributions. Second, we take helium as an example of multiphoton and multichannel interference dominated electron dynamics, by investigating the transient absorption of an isolated attosecond pulse in the presence of a femtosecond infrared laser pulse.
In this paper, by applying generalized density-matrix equations, we explore the ultrafast dynamics of photo-generated electron–hole pairs in the system composed of electromagnetically coupled GaAs/AlGaAs quantum dots and reveal the physics mechanism behind laser-controlled nonlinear-optical response of electron–hole pairs. For the single-dot system, we present numerical results to show the transient dependence of carrier occupations and induced quantum coherence of electron–hole pairs in the presence of either a single or double laser pulses, as well as for a step turning-on of the laser field. For a dipole-radiation coupled double-dot system, we study numerically the time dependence of both intradot and interdot self-consistent depolarization fields within and between two dots, respectively. Meanwhile, we further demonstrate the significance of phase matching between induced depolarization fields and incident-laser pulse in order to maximize the stimulated transitions of electron–hole pairs and ensure non-quenched Rabi oscillations in each quantum dot. The employed theoretical model and the associated numerical analysis method are expected to facilitate designing and developing artificial quantum molecules composed of arbitrarily dielectric-embedded quantum dots with non-local quantum interactions and entanglement, as well as optically manipulating electron states of artificial quantum molecules.
This thesis presents theoretical models and results of numerical simulations describing the propagation of optical pulses through dense, thermal atomic vapours. In particular we investigate the nonlinear effects of optical solitons due to self-induced transparency (SIT) in two-level systems, optical simultons in V-type three-level systems and electromagnetically induced transparency (EIT) in Λ-type systems, including the storage and retrieval of dark-state polaritons. An investigation is made into two-photon excitation of the 5D states of rubidium in a high-intensity beam including the hyperfine structure of the relevant atomic levels. Decay from these states to the 6P manifolds is ruled out as a cause of experimentally observed fluorescence due to the amount of power broadening associated with intensities necessary to provide any significant level of population in these highly excited states. We combine the nonlinear effects of optical solitons and EIT to explain experimentally observed steepened pulses in a V-type system in a micron-length cell. We explain the behaviour as the early formation of a simulton pulse drawn from a CW probe field by a strong coupling pulse, due to coherent population trapping. We predict that in a longer cell it may be possible to facilitate propagation of matched pulses, even when the transitions in the system have different propagation coefficients, as long as decoherence from collision broadening can be controlled. The fact that weak pulses can propagate with this scheme suggests an approach to achieving transparent propagation of single or few photon pulses distinct from, but related to, both SIT and EIT.
The authors develop a theoretical analysis which describes coherent nonlinear resonant effects where two optical pulses of different frequencies undergo two-photon self-induced transparency (two-photon SIT) in an inhomogeneously broadened three-level system. The field (Maxwell) and atomic (Schrodinger; density matrix representation) equations are coupled in a self-consistent manner by virtue of the resultant macroscopic polarizations at the two frequencies. This treatment is accomplished under circumstances where atomic coherence plays a predominant role. The resulting equations yield a new two-photon area theorem which gives first the intensity dependent, two-photon absorption law analogous to Beer's law for the one-photon transition. Secondly, a 2 pi Lorentzian pulse solution is derived which propagates without loss at the modified pulse velocity.