We show how a synthetic SSH lattice structure can inhibit the spontaneous emission of photons by a quantum emitter. Opening doors to optical approach to switching spontaneous emission on and off.
Engineering the photonic environment using lattices of coupled resonators, which we refer to as lattice quantum electrodynamics (QED), provides a route to control both the spontaneous emission of individual quantum emitters and the photon-mediated interactions between them. Here we introduce an optical lattice QED platform based on individual dibenzoterrylene (DBT) molecules embedded in anthracene crystals and coupled to lattices of open optical microcavities. This hybrid architecture benefits from narrow-linewidth molecular emitters, site-resolved optical access, engineered coupled-resonator bands, and compatibility with established molecular frequency-tuning techniques. As a proof-of-principle demonstration, we observe emitter-photon bound states formed when the optical transition of a single molecule is tuned to the band gap of a Su-Schrieffer-Heeger (SSH) cavity lattice. These in-gap states display directional localization and photon emission on a single sublattice, inherited from the vacancy-induced topological edge modes of the underlying SSH lattice. Our results establish open-cavity lattices coupled to DBT molecules as a versatile architecture for engineering many-emitter quantum optical systems with controllable photon-mediated interactions.
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.