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Conference on Lasers and Electro-Optics Europe & European Quantum Electronics Conference (CLEO/Europe-EQEC)

Switching spontaneous emission in microcavities in the time domain

Henri Thyrrestrup, Alex Hartsuiker, Jean‐Michel Gérard, Willem L. Vos

Published May 1, 2013• 0 citations
Publisher

Abstract

Impressive progress has been achieved in controlling the spontaneous emission rate for emitters in Nanophotonic structures, such as microcavities, photonic crystals and nano-antennas. In all cases, however, the modification of the emission is stationary in time. Thus, the emission rate is time-independent and the distribution of photon emission times are stochastic and follow an exponential distribution in the weak coupling regime. In this paper, by using fast all-optical switching of a microcavity, the cavity resonance is tuned within tens of picosesonds. This drastically changes the local optical density of states at the emission frequency within the emission lifetime of the emitters. This paper theoretically studied an ensemble of two-level sources with a time dependent decay rate and have derived the excited state population and emitted intensity as a function of time for continuous wave and pulsed excitation. Deterministic bursts of dramatically enhanced or inhibited emission intensity within short intervals. Thereby, we control the photon distribution to show behavior that strongly deviates from single exponential decay. This can be used to protect quantum information systems against decoherence and to realize non-Markovian dynamics in cavity quantum electrodynamics.

DOI
10.1109/cleoe-iqec.2013.6801876

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Impressive progress has been achieved in controlling the spontaneous emission rate for emitters in Nanophotonic structures, such as microcavities, photonic crystals and nano-antennas. In all cases, however, the modification of the emission is stationary in time. Thus, the emission rate is time-independent and the distribution of photon emission times are stochastic and follow an exponential distribution in the weak coupling regime. In this paper, by using fast all-optical switching of a microcavity, the cavity resonance is tuned within tens of picosesonds. This drastically changes the local optical density of states at the emission frequency within the emission lifetime of the emitters. This paper theoretically studied an ensemble of two-level sources with a time dependent decay rate and have derived the excited state population and emitted intensity as a function of time for continuous wave and pulsed excitation. Deterministic bursts of dramatically enhanced or inhibited emission intensity within short intervals. Thereby, we control the photon distribution to show behavior that strongly deviates from single exponential decay. This can be used to protect quantum information systems against decoherence and to realize non-Markovian dynamics in cavity quantum electrodynamics.
We have theoretically studied the effect of deterministic temporal control of spontaneous emission in a dynamic optical microcavity. We propose a new paradigm in light emission: we envision an ensemble of two-level emitters in an environment where the local density of optical states is modified on a time scale shorter than the decay time. A rate equation model is developed for the excited state population of two-level emitters in a time-dependent environment in the weak coupling regime in quantum electrodynamics. As a realistic experimental system, we consider emitters in a semiconductor microcavity that is switched by free-carrier excitation. We demonstrate that a short temporal increase of the radiative decay rate depletes the excited state and drastically increases the emission intensity during the switch time. The resulting time-dependent spontaneous emission shows a distribution of photon arrival times that strongly deviates from the usual exponential decay: A deterministic burst of photons is spontaneously emitted during the switch event.
The interaction of single quantum emitters with an optical cavity enables the realization of efficient spin-photon interfaces, an essential resource for quantum networks. The dynamical control of the spontaneous emission rate of quantum emitters in cavities has important implications in quantum technologies, e.g., for shaping the emitted photons' waveform or for driving coherently the optical transition while preventing photon emission. Here we demonstrate the dynamical control of the Purcell enhanced emission of a small ensemble of erbium ions doped into a nanoparticle. By embedding the nanoparticles into a fully tunable high finesse fiber based optical microcavity, we demonstrate a median Purcell factor of 15 for the ensemble of ions. We also show that we can dynamically control the Purcell enhanced emission by tuning the cavity on and out of resonance, by controlling its length with sub-nanometer precision on a time scale more than two orders of magnitude faster than the natural lifetime of the erbium ions. This capability opens prospects for the realization of efficient nanoscale quantum interfaces between solid-state spins and single telecom photons with controllable waveform, for non-destructive detection of photonic qubits, and for the realization of quantum gates between rare-earth ion qubits coupled to an optical cavity.
Spontaneous emission into micro- or nano-scale structures can be enhanced or inhibited by engineering the local density of optical states using closed quantum cavities. When electromagnetic fields are confined within small mode volumes of a high-Q symmetrical closed quantum cavity, the Purcell effect significantly accelerates the natural spontaneous emission. Due to the statistical nature of spontaneous emission, the emitted fields do not have a well-defined phase; consequently, the emission is incoherent and lacks directional control. The situation becomes more complicated in multi-mode cavities, as selecting a specific mode in a particular direction requires precise detuning between the emitter transition frequency and the cavity mode frequency to ensure strong coupling. In single-mode cavities, only the dominant mode can resonate, and only in a specific direction; thus, an appropriate transition frequency range can be easily determined. Such cavities allow for greater manipulation of the local electromagnetic density of states, facilitating effective control of the direction of spontaneous emission. This property is essential for creating efficient single-photon sources, photonic circuits, and on-chip quantum information.
We consider the process of spontaneous emission of a two-level atom embedded into a periodic layered dielectric structure. When the resonant atomic frequency lies within the photon-density-of-states gap, of width \ensuremath{\Gamma}, the atom emits light during a time interval t\ensuremath{\Gamma}\ensuremath{\ll}1 until the spontaneous emission becomes fully inhibited. We discuss the enhancing of spontaneous emission by tuning the atomic resonance with a one-mode microcavity. In the \ensuremath{\lambda}/4-shifted distributed feedback microcavities which possess the \ensuremath{\delta}-function-like density of states, in the middle of the gap, the process of spontaneous emission has damped Rabi oscillation behavior; the damping depends on the width of the gap and the height of its walls. A profile of the density-of-states gap can be determined from the experimental data on the temporal behavior of the atomic spontaneous decay.
Abstract The interaction of single quantum emitters with an optical cavity enables the realization of efficient spin-photon interfaces, an essential resource for quantum networks. The dynamical control of the spontaneous emission rate of quantum emitters in cavities has important implications in quantum technologies, e.g., for shaping the emitted photons’ waveform or for driving coherently the optical transition while preventing photon emission. Here we demonstrate the dynamical control of the Purcell enhanced emission of a small ensemble of erbium ions doped into a nanoparticle. By embedding the nanoparticles into a fully tunable high finesse fiber based optical microcavity, we demonstrate a median Purcell factor of 15 for the ensemble of ions. We also show that we can dynamically control the Purcell enhanced emission by tuning the cavity on and out of resonance, by controlling its length with sub-nanometer precision on a time scale more than two orders of magnitude faster than the natural lifetime of the erbium ions. This capability opens prospects for the realization of efficient nanoscale quantum interfaces between solid-state spins and single telecom photons with controllable waveform, for non-destructive detection of photonic qubits, and for the realization of quantum gates between rare-earth ion qubits coupled to an optical cavity.
Control of spontaneously emitted light lies at the heart of quantum optics. It is essential for diverse applications ranging from lasers, light-emitting diodes, solar cells, and quantum information. According to the quantum electrodynamics theory, the spontaneous emission (SE) of an atom can be a weak-coupling radiation process due to the vacuum fluctuations of electromagnetic field. A suitable modification of inhomogeneous environment is required so that the vacuum fluctuations controlling the SE can be manipulated. Inhibiting unwanted SE and boosting desired ones will promote the novel optoelectronic designs tailored to industrial standard. The local density of states (LDOS) counts the number of electromagnetic modes where photons can be emitted at the specific location of the emitter, and can be interpreted as the density of vacuum fluctuations. The inhibition or enhancement of SE boils down to how the LDOS of photons is controlled. In this work, the SE of the excited atoms in 2D arbitrary inhomogeneous environment has been systematically studied. The LDOS determines the radiation dynamics of a point source (for 3D) or a line source (for 2D). In particular, it also determines the SE rate, and the LDOS is represented by the electric dyadic Green’s function. The numerical solution of the electric Green’s tensor has been accurately obtained by the finite-difference frequency-domain method with the proper approximations of the monopole and dipole sources. The SE of the atoms in the photonic crystal and plasmonic metal plates has been comprehensively and comparatively investigated. For both systems, the SE strongly depends on their respective dispersion relations and could be modified or tuned by the finite-structure or finite-size effects. This work is important for the SE engineering and optimized design of optoelectronic devices.