Strong coupling between plasmons and excitons in nanocavities can result in the formation of hybrid plexcitonic states. Understanding the dispersion relation of plexcitons is important both for fundamental quantum science and for applications including optoelectronics and nonlinear optics devices. The conventional approach, based on statistics over different nanocavities, suffers from large inhomogeneities from the samples, owing to the nonuniformity of nanocavities and the lack of control over the locations and orientations of the excitons. Here we report the first measurement of the dispersion relationship of plexcitons in an individual nanocavity. Using a single silver nanorod as a Fabry-Pérot nanocavity, we realize strong coupling of plasmon in single nanocavity with excitons in a single atomic layer of tungsten diselenide. The plexciton dispersion is measured by in situ redshifting the plasmon energy via successive deposition of a dielectric layer. Room-temperature formation of plexcitons with Rabi splittings as large as 49.5 meV is observed. The realization of strong plasmon-exciton coupling by in situ tuning of the plasmon provides a novel route for the manipulation of excitons in semiconductors.

The interaction between plasmons in metal nanostructures and excitons in layered materials attracts recent interests due to its fascinating properties inherited from the two constituents, e.g., the high tunability on its spectral or spatial properties from the plasmonic component, and the large optical nonlinearity or light emitting properties from the excitonic counterpart. Here, we demonstrate light-emitting plexcitons from the coupling between the neutral excitons in monolayer WSe and highly confined nanocavity plasmons in the nanocube-over-mirror system. We observe, simultaneously, an anticrossing dispersion curve of the hybrid system in the dark-field scattering spectrum and a 1700 times enhancement in the photoluminescence. We attribute the large photoluminescence enhancement to the increased local density of states by both the plasmonic and excitonic constituents in the intermediate coupling regime. In addition, increasing the confinement of the hybrid systems is achieved by shrinking down the size of the hot spot within the gap between the nanocube and the metal film. Numerical calculations reproduce the experimental observations and provide the effective number of excitons taking part in the interaction. This highly compact system provides a room temperature testing platform for quantum cavity electromagnetics at the deep subwavelength scale.

Achieving strong coupling between emitters and photons in cavities holds an important position in the light-matter interaction due to the enabled applications such as polariton lasing, all-optical switches, and quantum...

Integration of plasmonic nanostructures with fiber‐optics‐based neural probes enables label‐free detection of molecular fingerprints via surface‐enhanced Raman spectroscopy (SERS), and it represents a fascinating technological horizon to investigate brain function. However, developing neuroplasmonic probes that can interface with deep brain regions with minimal invasiveness while providing the sensitivity to detect biomolecular signatures in a physiological environment is challenging, in particular because the same waveguide must be employed for both delivering excitation light and collecting the resulting scattered photons. Here, a SERS‐active neural probe based on a tapered optical fiber (TF) decorated with gold nanoislands (NIs) that can detect neurotransmitters down to the micromolar range is presented. To do this, a novel, nonplanar repeated dewetting technique to fabricate gold NIs with sub‐10 nm gaps, uniformly distributed on the wide (square millimeter scale in surface area), highly curved surface of TF is developed. It is experimentally and numerically shown that the amplified broadband near‐field enhancement of the high‐density NIs layer allows for achieving a limit of detection in aqueous solution of 10−7 m for rhodamine 6G and 10−5 m for serotonin and dopamine through SERS at near‐infrared wavelengths. The NIs‐TF technology is envisioned as a first step toward the unexplored frontier of in vivo label‐free plasmonic neural interfaces.