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.
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.
In this work, we develop a physically transparent Coulomb-interaction model from simplification of a general many-body theory and apply this model to study interacting electron dynamics for transient occupation and quantum coherence in both single and double quantum dots under laser irradiation. Our theory considers self-consistently the Coulomb-renormalized Rabi coupling to light by using an induced optical-depolarization field, corresponding to dynamical exchange interaction between two electrons within the same quantum dot. Meanwhile, we employ evanescent-field coupling for dynamical Coulomb interaction between two electrons in different quantum dots based on a surface-plasmon model. In particular, we explore the quantum interference between a pair of laser-induced quantum coherence in three-level quantum-dot systems, which gives rise to indirect transition of electrons for sum- and difference-frequency transient optical responses. By varying laser frequency detuning, the control of laser-dressed electronic states becomes possible and can be utilized for switching among off-state, partial, and complete on-states. This study will be useful for controlling the phase entanglement of two laser-dressed states of quantum dots, as well as for enhancing the electro-optical performance through sum- and difference-frequency transitions in many optoelectronic devices.
We provide a theoretical study for the dynamical behavior of two-photon Rabi oscillations in two coupled quantum dots. Each dot is a three-level quantum system (ground, one-exciton, and biexciton states). We describe the optical dynamics within the density matrix formalism framework. The two-photon Rabi oscillations are found to be significantly affected by the strength of the interdot dipolar interaction. Using a detuned laser pulse with an exciton state of the driven quantum dot in our numerical simulations, a direct coherent excitation between the biexciton states can be established, but whether Rabi oscillations can be observed depend mainly on the strength of the dipolar interaction and bandwidth of the excitation laser. When the strength of the dipolar coupling is less than the excitation laser bandwidth, the time-dependent populations of the various two biexciton states of the system exhibit coherent oscillations with several frequencies. However, as we increase the dipolar coupling strength, the population transfer between the quantum dots levels amazingly becomes forbidden, and the excitation gets trapped at the initial state. The reduction of the influence of the dipolar interaction leads to a manipulation of two-photon Rabi oscillation in an ultrashort timescale (∼ps), opening possibilities to achieve ultrafast quantum state control and quantum logic gate generation.
We theoretically investigate the use of random, self-organized clusters of strain-coupled QDMs for coherent laser control experiments. As a first step, we do not rely on entangled states, but describe the array of QDMs in a time-dependent Hartree-picture. The individual electrons, confined to separate QDMs, are treated as two-level quantum oscillators, which are coupled by long-range Coulomb interactions. The dynamics of the system under the influence of coherent classical laser fields is then calculated by solving the coupled density matrix equations for the electrons. We consider various possible experiments of increasing complexity (including nonlinear absorption, selective bleaching and coherent emission), which would allow to achieve and/or confirm the mutual coupling of the oscillators.
A model of semiconductor quantum dots coupled to phonons and laser light, which is relevant in the limit of strong electronic confinement, is investigated. For an arbitrary sequence of excitations by ultrafast pulses, analytical solutions are obtained for all pertinent density-matrix elements. The results are nonperturbative with respect to the coupling to both phonons and laser light. The derivation depends neither on a particular choice of electronic wave functions nor on a particular wave-vector dependence of the phonon interaction or phonon dispersion. All components of the density matrix exhibit oscillatory dependences on the pulse areas of the exciting pulses analogously to the Rabi oscillations known from simple two-level systems. Three typical applications of the general results are worked out: (a) the influence of phonons on four-wave-mixing spectra, (b) the coherent control of electronic dot occupations in the presence of phonons, and (c) the dynamics of phonon correlations including the formation of a stable polaron spatially localized in the dot and the emission of a pulsed phonon wave packet that leaves the dot.
This study investigates the tunable propagation of optical pulses in a three-level system of coupled quantum dots. The system forms an effective closed configuration, supporting strong quantum coherence and controllable light–matter interactions. Using the density matrix formalism, we analyze the quantum dynamical response under the influence of both a weak probe and a strong control field, with inter-dot tunneling acting as a key tunable parameter. Our results reveal that both the tunneling strength (Te) and control field Rabi frequency (Ωc) play crucial roles in shaping the system’s optical properties. We observe the emergence of electromagnetically induced transparency-like windows, the splitting and shifting of dispersion peaks, and the formation of absorption doublets and transparency windows. The real and imaginary parts of the electric permittivity exhibit pronounced sensitivity to these external controls. Furthermore, the group index and group velocity are shown to be highly tunable, enabling transitions between slow-light and fast-light regimes. Detailed analysis of temporal pulse dynamics demonstrates the ability to achieve controllable delay and advancement of optical pulses, depending on the interaction between Te and Ωc. These findings highlight the potential of such quantum dot systems for dynamic photonic control, including applications in optical buffering, reconfigurable delay lines, coherent switching, and quantum information processing. The demonstrated tunability and coherence effects make this platform a promising candidate for next-generation optoelectronic and quantum photonic technologies.
A theory of both linear and nonlinear electromagnetic responses of a single quantum dot (QD) exposed to quantum light, accounting for depolarization induced local field has been developed. Based on the microscopic Hamiltonian accounting for the electron-hole exchange interaction, an effective two-body Hamiltonian has been derived and expressed in terms of the incident electric field, with a separate term describing the QD depolarization. The quantum equations of motion have been formulated and solved using the Hamiltonian for various types of the QD optical excitation, such as Fock qubit, coherent fields, vacuum state of electromagnetic field, and light with arbitrary photonic state distribution. For a QD exposed to coherent light, we predict the appearance of two oscillatory regimes in the Rabi effect separated by the bifurcation. In the first regime, the standard collapse-revival phenomenon does not reveal itself and the QD population inversion is found to be negative, while in the second one, the collapse-revival picture is found to be strongly distorted as compared to that predicted by the standard Jaynes-Cummings model. For the case of QD interaction with an arbitrary quantum light state in the linear regime, it has been shown that the local field induces a fine structure of the absorbtion spectrum. Instead of a single line with frequency corresponding to the exciton transition frequency, a duplet appears, with one component shifted by the amount of the local field coupling parameter. It has been demonstrated that the strong light--matter coupling regime arises in the weak-field limit. A physical interpretation of the predicted effects has been proposed.