The spontaneous emission rate of dipole emitters close to plasmonic dimers are theoretically studied within a nonlocal hydrodynamic model. A nonlocal model has to be used since quantum emitters in the immediate environment of a metallic nanoparticle
probe its electronic structure. Compared to local calculations, the emission rate is significantly reduced. The influence is mostly pronounced if the emitter is located close to sharp edges. We suggest to use quantum emitters to test nonlocal effects in experimentally feasible configurations.
An optical nanoantenna and adjacent atomic systems are strongly coupled when an excitation is repeatedly exchanged between these subsystems prior to its eventual dissipation into the environment. It remains challenging to reach the strong coupling re
gime but it is equally rewarding. Once being achieved, promising applications as signal processing at the nanoscale and at the single photon level would immediately come into reach. Here, we study such hybrid configuration from different perspectives. The configuration we consider consists of two identical atomic systems, described in a two-level approximation, which are strongly coupled to an optical nanoantenna. First, we investigate when this hybrid system requires a fully quantum description and provide a simple analytical criterion. Second, a design for a nanoantenna is presented that enables the strong coupling regime. Besides a vivid time evolution, the strong coupling is documented in experimentally accessible quantities, such as the extinction spectra. The latter are shown to be strongly modified if the hybrid system is weakly driven and operates in the quantum regime. We find that the extinction spectra depend sensitively on the number of atomic systems coupled to the nanoantenna.
