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Science

Coherent Optical Control of the Quantum State of a Single Quantum Dot

N. H. Bonadeo, John Erland, Dan Gammon, D. Park, Douglas Scott Katzer, Duncan G. Steel

Published Nov 20, 1998• 643 citations
Publisher

Abstract

Picosecond optical excitation was used to coherently control the excitation in a single quantum dot on a time scale that is short compared with the time scale for loss of quantum coherence. The excitonic wave function was manipulated by controlling the optical phase of the two-pulse sequence through timing and polarization. Wave function engineering techniques, developed in atomic and molecular systems, were used to monitor and control a nonstationary quantum mechanical state composed of a superposition of eigenstates. The results extend the concept of coherent control in semiconductors to the limit of a single quantum system in a zero-dimensional quantum dot.

DOI
10.1126/science.282.5393.1473

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Picosecond optical excitation was used to coherently control the excitation in a single quantum dot on a time scale that is short compared with the time scale for loss of quantum coherence. The excitonic wave function was manipulated by controlling the optical phase of the two-pulse sequence through timing and polarization. Wave function engineering techniques, developed in atomic and molecular systems, were used to monitor and control a nonstationary quantum mechanical state composed of a superposition of eigenstates. The results extend the concept of coherent control in semiconductors to the limit of a single quantum system in a zero-dimensional quantum dot.
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.
We demonstrate that a matter physical two-level system, a qubit, can be fully controlled using one ultrafast step. We show that the spin state of an optically excited electron, an exciton, confined in a quantum dot, can be rotated by any desired angle, about any desired axis, during such a step. For this we use a single, resonantly tuned, picosecond long, polarized optical pulse. The polarization of the pulse defines the rotation axis, while the pulse detuning from a nondegenerate absorption resonance defines the magnitude of the rotation angle. We thereby achieve a high fidelity, universal gate operation, applicable to other spin systems, using only one short optical pulse. The operation duration equals the pulse temporal width, orders of magnitude shorter than the qubit evolution life and coherence times.
The strong confinement of semiconductor excitons in a quantum dot gives rise to atomlike behavior. The full benefit of such a structure is best observed in resonant excitation where the excited state can be deterministically populated and coherently manipulated. Because of the large refractive index and device geometry it remains challenging to observe resonantly excited emission that is free from laser scattering in III/V self-assembled quantum dots. Here we exploit the biexciton binding energy to create an extremely clean single photon source via two-photon resonant excitation of an InAs/GaAs quantum dot. We observe complete suppression of the excitation laser and multiphoton emissions. Additionally, we perform full coherent control of the ground-biexciton state qubit and observe an extended coherence time using an all-optical echo technique. The deterministic coherent photon pair creation makes this system suitable for the generation of time-bin entanglement and experiments on the interaction of photons from dissimilar sources.
We present a series of coherent nonlinear optical experiments that show semiconductor quantum dots have optical properties very similar to simple atomic systems but are surprisingly robust against decoherence and have large dipole moments. By combining advances in nano-optical probing methodologies with the power of coherent nonlinear optical spectroscopy techniques, the measurements have enabled us to extend concepts of coherent optical control and wave function engineering to a single quantum dot exciton.
We report on coherent control of the fundamental exciton state in a single quantum dot by means of two phase-locked picosecond laser pulses. By analyzing the experiments performed in the Rabi regime and comparing them to numerical simulations, we show that we can address the exciton coherence and get an insight into the involved dephasing processes. The total decoherence time T2{T}_{2}T2​ (170 ps) is comparable to the effective exciton lifetime T1{T}_{1}T1​ (200 ps), although not reaching the upper theoretical limit of 2T12{T}_{1}2T1​. We conclude that energy relaxation and pure dephasing processes due to virtual scattering with phonons both contribute on an equal footing to the loss of coherence in this kind of monolayer-step-induced GaAs quantum dots.
We demonstrate high-fidelity reversible transfer of quantum information from the polarization of photons into the spin state of an electron-hole pair in a semiconductor quantum dot. Moreover, spins are electrically manipulated on a subnanosecond time scale, allowing us to coherently control their evolution. By varying the area of the electrical pulse, we demonstrate phase-shift and spin-flip gate operations with near-unity fidelities. Our system constitutes a controllable quantum interface between flying and stationary qubits, an enabling technology for quantum logic in the solid state.