Thermal effects on photon-induced quantum transport in a single quantum dot.

We theoretically investigate laser induced quantum transport in a single quantum dot attached to electrical contacts. Our approach, based on a nonequilibrium Green function technique, allows us to include thermal effects on the photon-induced quantum transport and excitonic dynamics, enabling the study of non-Markovian effects. By solving a set of coupled integrodifferential equations, involving correlation and propagator functions, we obtain the photocurrent and the dot occupation as a function of time. Two distinct sources of decoherence, namely, incoherent tunneling and thermal fluctuations, are observed in the Rabi oscillations. As temperature increases, a thermally activated Pauli blockade results in a suppression of these oscillations. Additionally, the interplay between photon and thermally induced electron populations results in a switch of the current sign as time evolves and its stationary value can be maximized by tuning the laser intensity.

Electrical control of interdot electron tunneling in a double InGaAs quantum-dot nanostructure.

We employ ultrafast pump-probe spectroscopy to directly monitor electron tunneling between discrete orbital states in a pair of spatially separated quantum dots. Immediately after excitation, several peaks are observed in the pump-probe spectrum due to Coulomb interactions between the photogenerated charge carriers. By tuning the relative energy of the orbital states in the two dots and monitoring the temporal evolution of the pump-probe spectra the electron and hole tunneling times are separately measured and resonant tunneling between the two dots is shown to be mediated both by elastic and inelastic processes. Ultrafast (<5 ps) interdot tunneling is shown to occur over a surprisingly wide bandwidth, up to ∼8 meV, reflecting the spectrum of exciton-acoustic phonon coupling in the system.

Dephasing of exciton polaritons in photoexcited InGaAs quantum dots in GaAs nanocavities.

We present a combined experimental and theoretical study of the emission spectrum of zero dimensional nanocavity polaritons in electrically tunable single dot nanocavities. Such devices allow us to vary the dot-cavity detuning in situ and probe the emission spectrum under well-controlled conditions of lattice temperature and incoherent excitation level. Our results show that the observation of a double peak in the emission spectrum is not an unequivocal signature of strong coupling. Moreover, by comparing our results with theory, we extract the effective vacuum Rabi splitting, the pure dephasing rate, and their dependence on the incoherent optical pumping power and lattice temperature. Our study highlights how coupling to the lattice and dynamical fluctuations in the solid-state environment influence the coherence properties of quantum dot microcavity polaritons and, sometimes, may mask the occurrence of strong coupling.

Decoherence of rabi oscillations in a single quantum dot.

We develop a realistic model of Rabi oscillations in a quantum-dot photodiode. Based in a multiexciton density matrix formulation we show that for short pulses the two-level model fails and higher levels should be taken into account. This affects some of the experimental conclusions, such as the inferred efficiency of the state rotation (population inversion) and the deduced value of the dipole interaction. We also show that the damping observed cannot be explained using constant rates with fixed pulse duration. We demonstrate that the damping observed is in fact induced by an off-resonant excitation to or from the continuum of wetting layer states. Our model describes the nonlinear decoherence behavior observed in recent experiments.