A combined process of electropolishing, focused-ion-beam lithography, and controlled anodization is used to fabricate anodic alumina films with ordered nanochannels. The ion beam is used to create a hexagonally close-packed lattice of concaves on a polished aluminum surface and the concaves act as pinning points for guiding the growth of nanochannels in the following anodization step. By carefully matching the lattice constant (100 nm) with the anodization voltage, ordered nanochannels with aspect ratio of ∼100 are fabricated. The effects of the ion dose and its corresponding depth of the concaves on the ordering of the nanochannel array are investigated and a minimum depth of 3 nm is found to be necessary for effective guidance of the growth of ordered nanochannels.

Long-range ordered arrays of anodic alumina nanochannels are grown by anodizing an aluminum covered with a patterned layer of polymethylmethacrylate (PMMA) resist. The two-dimensional hexagonal-closed-packed pattern is created by focused ion beam (FIB) exposure of the PMMA and transferred onto the aluminum surface by phosphoric acid etching. The required exposure time per channel is only $\text{∼20\hspace{0.17em}μ}\mathrm{s},$ more than two orders of magnitude reduction in comparison with the previous method employing FIB direct sputtering of the aluminum surface.

The authors report experimental studies of surface-enhanced Raman scattering (SERS) of wurtzite-type GaN and ZnO crystalline samples covered with Ag-nanoparticles. The longitudinal optical phonons consistently exhibit unusually intense Raman enhancement in comparison with other phonons. The anomaly is interpreted by a proposed model based on a resonant Raman scattering process assisted by metal-induced gap states at the Ag/GaN and Ag/ZnO interfaces. This study suggests that SERS of lattice vibrations in inorganic semiconductors is sensitive to their propagation nature, providing a progressive perspective view on electron-mediated enhanced Raman scattering.

We report on strong plasmonic coupling from silver nanoparticles covered by hydrogen-terminated chemically vapor deposited single-layer graphene, and its effects on the detection and identification of adenine molecules through surface-enhanced Raman spectroscopy (SERS). The high resistivity of the graphene after subjecting to remote plasma hydrogenation allows plasmonic coupling induced strong local electromagnetic fields among the silver nanoparticles to penetrate the graphene, and thus enhances the SERS efficiency of adenine molecules adsorbed on the film. The graphene layer protects the nanoparticles from reactive and harsh environments and provides a chemically inert and biocompatible carbon surface for SERS applications.