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arXiv:1805.06357 · Physical Review Letters

Wigner Time Delay Induced by a Single Quantum Dot

Max Strauß, Alexander Carmele, Julian Schleibner, Marcel Hohn, Christian Schneider, Sven Höfling, Janik Wolters, Stephan Reitzenstein

Published Mar 13, 2019• 13 citations
arXivHTMLPDF

Abstract

Resonant scattering of weak coherent laser pulses on a single two-level system realized in a semiconductor quantum dot is investigated with respect to a time delay between incoming and scattered light. This type of time delay was predicted by Wigner in 1955 for purely coherent scattering and was confirmed for an atomic system in 2013 [R. Bourgain et al., Opt. Lett. 38, 1963 (2013)OPLEDP0146-959210.1364/OL.38.001963]. In the presence of electron-phonon interaction, we observe deviations from Wigner's theory related to incoherent and strongly non-Markovian scattering processes which are hard to quantify via a detuning-independent pure dephasing time. We observe detuning-dependent Wigner delays of up to 530 ps in our experiments which are supported quantitatively by microscopic theory allowing for pure dephasing times of up to 950 ps.

DOI
10.1103/physrevlett.122.107401

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Resonant scattering of weak coherent laser pulses on a single two-level system realized in a semiconductor quantum dot is investigated with respect to a time delay between incoming and scattered light. This type of time delay was predicted by Wigner in 1955 for purely coherent scattering and was confirmed for an atomic system in 2013 [R. Bourgain et al., Opt. Lett. 38, 1963 (2013)OPLEDP0146-959210.1364/OL.38.001963]. In the presence of electron-phonon interaction, we observe deviations from Wigner's theory related to incoherent and strongly non-Markovian scattering processes which are hard to quantify via a detuning-independent pure dephasing time. We observe detuning-dependent Wigner delays of up to 530 ps in our experiments which are supported quantitatively by microscopic theory allowing for pure dephasing times of up to 950 ps.
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 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 analyze the light scattered by a single InAs quantum dot interacting with a resonant continuous-wave laser. High-resolution spectra reveal clear distinctions between coherent and incoherent scattering, with the laser intensity spanning more than four orders of magnitude. We find that the fraction of coherently scattered photons can approach unity under sufficiently weak or detuned excitation, ruling out pure dephasing as a relevant decoherence mechanism. We show how spectral diffusion shapes spectra, correlation functions, and phase coherence, concealing the ideal radiatively broadened two-level system described by Mollow.
The interaction between photons and a single two-level atom constitutes a fundamental paradigm in quantum physics. The nonlinearity provided by the atom leads to a strong dependence of the light-matter interface on the number of photons interacting with the two-level system within its emission lifetime. This nonlinearity unveils strongly correlated quasiparticles known as photon bound states, giving rise to key physical processes such as stimulated emission and soliton propagation. Although signatures consistent with the existence of photon bound states have been measured in strongly interacting Rydberg gases, their hallmark excitation-number-dependent dispersion and propagation velocity have not yet been observed. Here we report the direct observation of a photon-number-dependent time delay in the scattering off a single artificial atom-a semiconductor quantum dot coupled to an optical cavity. By scattering a weak coherent pulse off the cavity-quantum electrodynamics system and measuring the time-dependent output power and correlation functions, we show that single photons and two- and three-photon bound states incur different time delays, becoming shorter for higher photon numbers. This reduced time delay is a fingerprint of stimulated emission, where the arrival of two photons within the lifetime of an emitter causes one photon to stimulate the emission of another.
Excitons in quantum dots represent a remarkably good two-level system with a large optical dipole transition moment. Although most research currently focuses on enhancing their already outstanding properties as single photon emitters they become also increasingly interesting for experimental fundamental research due to their large dipole transition moment. This thesis presents studies which explore fundamental phenomena in quantum dots using coherent spectrocopy methods. First, we will first examine the optical properties of site-controlled quantum dots which were grown using a buried stressor via resonance fluorescence. Subsequently, we will show results that were obtained using photocurrent spectroscopy to study single quantum dots that are embedded in micropillar resonators. This is followed by a study of the Wigner time delay induced by a single quantum dot and which shows that the maximum delay is larger than its dephasing time T2 which is the theoretical limit for coherently scattered fraction. The next section demonstrates that the response of a resonantly driven two-level system which in our case is represented by an exciton in a seminconductor quantum dot depends significantly on the photon statistics of the exciting light field. Most strikingly, the Mollow triplet which we observe under coherent excitation vanishes under thermal excitation. The second part presents results concerned with the resonantly driven biexciton cascade via two- photon excitation. The coherent interaction between light field and excitons gives rise to a complex five-level system. Here, we show for the first time two-photon Rabi oscillations in the temporal domain. Furthermore, we examine the correlations between the different transitions. The measurements show that we can manipulate the time-ordering of the emitted photons by changing for example the laser power. All these studies share the resonant excitation scheme which allows for a coherent manipulation of the states of the quantum dot and grants access to phenomena typical for resonance fluorescence such as the Mollow triplet and Rabi oscillations. In particular the experiments on photon excitation spectroscopy and the studies on the dressed biexciton cascade show that fundamental effects of quantum optics can be explored in a scalable and application oriented setting using quantum dots.
In this thesis, the coherent interaction of single semiconductor quantum dots and ultrafast optical pulses is studied. Under certain conditions, localized exciton transitions in quantum dots can be seen as semi-isolated two-level systems. While this description is sufficient for the explanation of some observations in coherent experiments, it is sometimes necessary to explicitly consider coupling of the discreet quantum states confined to the dot with the environment. We start out from simple, classical examples of coherent spectroscopy and then turn towards experiments where the interaction with the vicinity of the dot becomes an important factor. First, a novel method for transient differential reflectivity spectroscopy of single quantum systems is introduced. It is a pure far-field optical technique which does not require any sophisticated sample preparation steps which makes it applicable to a broad range of structures. Pump pulses excite the sample structure and probe pulses read out the pump-induced changes in the system after a variable delay time. In the case of a single dipole, the signal is given in the form of the spectral inteferogram between the backscattered wave from the particle and the probe light which is reflected at the sample surface. This form of homodyne detection amplifies the weak scattered wave from the particle and thus makes this kind of spectroscopy for single quantum dots feasible. In the remainder of this thesis our spectroscopic method is applied to either characterize the coherent properties of single quantum dots, to prepare and read-out a desired quantum state or to deliberately manipulate them. Coherence times and oscillator strengths are determined for localized exciton transitions. Arbitrary population states can be written by driving coherent population oscillations using resonant pulses, while entangled superpositions of two exciton states in a single dot are investigated by quantum beats on transient differential spectra. We finally exploit the interaction between the dot and a nearby absorbing layer to switch the dot's absorption spectrum on ultrafast timescales via light-induced transient electric fields.