We report direct observation of the strong exciton-photon coupling in a ZnO tapered whispering gallery (WG) microcavity at room temperature. By scanning excitations along the tapered arm of the ZnO tetrapod using a micro-photoluminescence spectrometer with different polarizations, we observed a transition from the pure WG optical modes in the weak interaction regime to the excitonic polariton in the strong coupling regime. The experimental observations are well described by using the plane wave model including the excitonic polariton dispersion relation. This provides a direct mapping of the polariton dispersion, and thus a comprehensive picture for coupling of different excitons with differently polarized WG modes.
We demonstrate a novel way to realize room-temperature polariton parametric scattering in a one-dimensional ZnO microcavity. The polariton parametric scattering is driven by a polariton condensate, with a balanced polariton pair generated at the adjacent polariton mode. This parametric scattering is experimentally investigated by the angle-resolved photoluminescence spectroscopy technique under different pump powers and it is well described by the rate equation of interacting bosons. The direct relation between the intensity of the scattered polariton signal and that of the polariton reservoir is acquired under nonresonant excitation, exhibiting the explicit nonlinear characteristic of this room-temperature polariton parametric process.
The strong coupling between excitons and Fabry-Pérot (F-P) cavity modes in tungsten sulfide (WS2) thin layers was studied. By using home-made micro-reflectance spectroscopic technique, we observed the anti-crossing behavior between cavity mode and excitons with flake's thickness dependence. Giant Rabi splitting of ~270 meV for A exciton and ~780 meV for B exciton were obtained from the fitting of the cavity polariton dispersions by use of the coupled oscillators model.
Organic-inorganic halide perovskite semiconductors with the attractive physics properties, including strong photoluminescence (PL), huge oscillator strengths, and low nonradiative recombination losses, are ideal candidates for studying the light-matter interaction in nanostructures. Here, we demonstrate the coupling of the exciton state and the cavity mode in the lead halide perovskite microcavity system at room temperature. The Purcell effect in the coupling system is clearly observed by using angle-resolved photoluminescence spectra. Kinetic analysis based on time-resolved PL reveals that the spontaneous emission rate of the halide perovskite semiconductor is significantly enhanced at resonance of the exciton energy and the cavity mode. Our results provide the way for developing electrically driven organic polariton lasers, optical devices, and on-chip coherent quantum light sources.
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