Optical properties of nanowire dimers with a spatially nonlocal dielectric function.

We study the optical spectra and electromagnetic field enhancements around cylindrical and triangular Ag nanowire dimers, allowing for a spatially nonlocal dielectric function that partially accounts for quantum mechanical effects. For the triangular structures, we pay particular attention to how these properties depend on the sharpness of the nanowire's tips. We demonstrate that significant differences exist from classical electrodynamics that employs a more common, spatially local dielectric function. These differences are shown to arise from the optical excitation of volume plasmons inside of the structures, analogous to one-particle quantum mechanical states, which lead to complex and striking patterns of material polarization. These results are important for further understanding the optical properties of structures at the nanoscale and have implications for numerous physical processes, such as surface-enhanced Raman scattering.