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.
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.
In 1946, E. M. Purcell predicted that the radiative lifetime of an emitter is not an intrinsic property but can be modified by structuring the surrounding electromagnetic field [36]. By inserting a semiconductor quantum dot (QD) in an optical cavity, one can accelerate or inhibit its spontaneous emission. In the present article, we show that the QD spontaneous emission can be deterministically controlled to fabricate bright sources of quantum light. QDs in cavities: basics, motivation, first demonstrations Light-matter coupling We note f the ground state of the QD and e its excited state. For a cavity mode close to resonance with the QD optical transition, we consider only the states with 0 or 1 photon in the cavity mode. The states ∣ e, 0〉 and ∣ f, 1〉 are coupled through light–matter interaction, with a constant g , where h g = ∣〈 e, 0∣ Ed ∣ f, 1∣, with d the dipole of the optical transition e → f and E the electric field at the QD position. Each of the states ∣ e, 0 > and ∣ f, 1 > are also coupled to continua of states: continuum of the free-space optical mode, phonons of the semiconductor matrix, etc. [4]. Here, we consider only the coupling to the continuum of the free-space optical mode, related to the cavity losses, with a constant γ c . When g << γ c , the photon emitted by the recombination of an exciton efficiently escapes outside the cavity. The QD optical transition radiative recombination rate can be accelerated (Purcell effect) or inhibited.
Solid-state quantum emitters such as the N-V center in diamond have applications ranging from single-photon sources to quantum sensors, with some quantum properties preserved even under ambient conditions. A central challenge is to access these quantum properties efficiently, by catching as much emitted light as possible. In this study a tunable optical microcavity, with a mode volume as small as one wavelength cubed, is used to enhance spontaneous emission of single N-V centers in diamond, via the Purcell effect. This allows the authors to extract large amounts of light from several individually addressable emitters, and to control their spontaneous-emission rate.
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.
Introduction Ever since 1916/17 when Einstein argued [45] [46] that spontaneous emission must occur if matter and radiation are to achieve thermal equilibrium, physicists have believed that spontaneous emission is an inherent quantum mechanical property of atoms and that excited atoms inevitably radiate. This view, however, overlooks the fact that spontaneous emission is a consequence of the coupling of quantized energy states of atoms with the quantized radiation field, and is a manifestation of quantum noise or of emission ‘stimulated’ by ‘vacuum fluctuations’. An infinity of vacuum states is available to the photon radiated by an excited atom placed in free space, leading to the effective irreversibility of such emissions. If these vacuum states are modified, as for example by placing an excited atom between closely spaced mirrors or in a small cavity (essentially the Casimir effect), spontaneous emission can be greatly inhibited or enhanced or even made reversible. Recent advances in atomic and optical techniques have made it possible to control and manipulate spontaneous emission. A whole new branch of quantum optics called ‘cavity QED’ has developed since 1987 utilizing these dramatic changes in spontaneous emission rates in cavities to construct new kinds of microscopic masers or micromasers that operate with a single atom and a few photons or with photons emitted in pairs in a two-photon transition.
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.
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.