Tightly confined plasmons in metal nanogaps are highly sensitive to surface inhomogeneities and defects due to the nanoscale optical confinement, but tracking and monitoring their location is hard. Here, we probe a 1-D extended nanocavity using a plasmonic silver nanowire (AgNW) on mirror geometry. Morphological changes inside the nanocavity are induced locally using optical excitation and probed locally through simultaneous measurements of surface enhanced Raman scattering (SERS) and dark-field spectroscopy. The increasing molecular SERS intensity and corresponding redshift of cavity plasmon modes by up to 60 nm indicate atomic-scale changes inside the nanocavity. We correlate this to diffusion of silver atoms into the nanogap, which reduces the nanogap size and enhances the optical near-field, enhancing the SERS. These induced changes can be locally excited at specific locations along the length of the nanowire and remain stable and nonreversible. Polymer surface coating on the AgNW affects the power threshold for inducing atom migration and shows that strong polyvinylpyrrolidone (PVP)- Ag binding gives rise to higher power thresholds. Such extended nanogap cavities are an ideal system to provide robust SERS while withstanding high laser powers. These results provide insights into the inhomogeneities of NW nanocavities and pave the way toward spatially controlled NW lithography in ambient conditions.
© 2024 The Authors. Published by American Chemical Society.