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Physical Review B

Direct detection of time-resolved Rabi oscillations in a single quantum dot via resonance fluorescence

John R. Schaibley, A. P. Burgers, Gregory A. McCracken, Duncan G. Steel, A. S. Bracker, Dan Gammon, Lu Jeu Sham

Published Mar 19, 2013• 34 citations
Publisher

Abstract

Optical Rabi oscillations are coherent population oscillations of a two-level system coupled by an electric dipole transition when driven by a strong nearly resonant optical field. In quantum dot structures, these measurements have typically been performed as a function of the total pulse area $\ensuremath{\int}{\ensuremath{\Omega}}_{0}(t)\phantom{\rule{0.16em}{0ex}}\mathrm{d}t$ where the pulse area varies as a function of Rabi frequency. Here, we report direct detection of the time-resolved coherent transient response of the resonance fluorescence to measure the time evolution of the optical Rabi oscillations in a single charged InAs quantum dot. We extract a decoherence rate consistent with the limit from the excited state lifetime.

DOI
10.1103/physrevb.87.115311

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Optical Rabi oscillations are coherent population oscillations of a two-level system coupled by an electric dipole transition when driven by a strong nearly resonant optical field. In quantum dot structures, these measurements have typically been performed as a function of the total pulse area \ensuremath∫\ensuremathΩ0(t)dt\ensuremath{\int}{\ensuremath{\Omega}}_{0}(t)\phantom{\rule{0.16em}{0ex}}\mathrm{d}t\ensuremath∫\ensuremathΩ0​(t)dt where the pulse area varies as a function of Rabi frequency. Here, we report direct detection of the time-resolved coherent transient response of the resonance fluorescence to measure the time evolution of the optical Rabi oscillations in a single charged InAs quantum dot. We extract a decoherence rate consistent with the limit from the excited state lifetime.
Transient nonlinear optical spectroscopy, performed on excitons confined to single GaAs quantum dots, shows oscillations that are analogous to Rabi oscillations in two-level atomic systems. This demonstration corresponds to a one-qubit rotation in a single quantum dot which is important for proposals using quantum dot excitons for quantum computing. The dipole moment inferred from the data is consistent with that directly obtained from linear absorption studies. The measurement extends the artificial atom model of quantum dot excitonic transitions into the strong-field limit, and makes possible full coherent optical control of the quantum state of single excitons using optical pi pulses.
Measurements of optical Rabi oscillations in the excited states of individual InGaAs are presented. Under pulsed resonant excitation we observe Rabi oscillations with increasing pulse area, which are damped after the first maximum and minimum. We show that the observed damping comes from an additional non-resonant generation of carriers in the quantum dot. The observation of Rabi oscillations provides an efficient way of directly measuring the excitonic transitions' dipole moments. A polarization anisotropy of the dipole moment is resolved in some of the quantum dots.
We report on coherent control of the resonantly driven exciton state in a single quantum dot in the strong coupling regime. With picosecond laser pulses, the two-level system undergoes Rabi oscillations and a given coherent superposition of states can be addressed. Using a pair of phase-locked pulses, optical manipulation is achieved during the coherence time of the qu-bit. The dephasing processes are also studied and we show that in typical quantum dots, the coherence time T 2 can be of the same order of magnitude as the effective lifetime of the exciton T 1 (a few hundreds of ps) although not reaching the upper theoretical limit of 2T 1 . We conclude that energy relaxation and pure dephasing processes due to virtual scattering with phonons contribute on an equal footing to the loss of coherence.