Control Of Spontaneous Emission Rate Research Articles

Control of spontaneous emission rate in lead halide perovskite film on hyperbolic metamaterial

Hyperbolic metamaterials represent a class of nanophotonic architectures with the possibility of controlling density of optical states. Due to this property, hyperbolic metamaterials can be employed as meta-electrodes in optoelectronic devices. On the other hand, lead halide perovskites have several promising properties for application in light-emitting devices. Moreover, a perovskite film is easily deposited on a hyperbolic metamaterial surface. Here, we theoretically show how to accelerate radiative recombination in a perovskite film with a hyperbolic metamaterial. This effect can be applied in light-emitting devices, where radiative recombination is extremely important.

Dynamic control of spontaneous emission rate using tunable hyperbolic metamaterials.

We numerically investigate the dynamic control over the spontaneous emission rate of quantum emitters using tunable hyperbolic metamaterials (HMMs). The dispersion of a metal-dielectric thin-film stack at a given frequency can undergo a topological transition from an elliptical to a hyperbolic dispersion by incorporating a tunable metal or dielectric film in the HMM. This transition modifies the local density of optical states of the emitter and, hence, its emission rate. In the visible range, we use an HMM consisting of TiN and ${{\rm Sb}_2}{{\rm S}_3}$Sb2S3 and show considerable tunability in the Purcell enhancement and quantum efficiency as ${{\rm Sb}_2}{{\rm S}_3}$Sb2S3 phase changes from amorphous to crystalline. Similarly, we show tunable Purcell enhancement in the telecommunication wavelength range using a ${\rm TiN}/{{\rm VO}_2}$TiN/VO2- HMM. Finally, tunable spontaneous emission rate in the mid-IR range is obtained using a ${\rm graphene}/{\rm MgF}_2$graphene/MgF2 HMM by modifying the graphene conductivity through changing its chemical potential. We show that using a metal nitride (for the visible and NIR HMMs) and a fluoride (for the mid-IR HMM) is important to get an appreciable change in the effective permittivity of the thin-film multilayer stack.

Control of spontaneous emission rate in luminescent resonant diamond particles

We study the properties of luminescent diamond particles of different sizes (up to ~1.5 μm) containing multiple NV-centers. We theoretically predict that the average liftetime in such particles is decreased by several times as compared to optically small subwavelength nanodiamonds. In our experiments, samples were obtained by milling the plasma-enhanced chemical vapor deposited diamond film, and characterized by Raman spectroscopy and dark- field spectroscopy methods. Time-resolved luminescence measurements of the excited state of NV-centers showed that their average lifetime varies from 10 to 17 ns in different samples. By comparing this data to the values of the lifetime of the NV-centers in optically small nanodiamonds, known from literature, we confirm a severalfold decrease of the lifetime in resonant particles.