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We have reported on the synthesis of ordered hexagonal Au nanoparticle (NPs) arrays by anodic alumina oxide templates (AAO)-assisted thermal treatment. This simple process has led to the formation of an ordered hexagonal array of Au NPs on the surface of AAO. SERS properties of the ordered hexagonal Au NPs could be obtained by varying the size of Au NPs. Compared with the Au thin film on AAO, the SERS intensity of rhodamine adsorbed on the ordered hexagonal Au NPs was about 1000 times stronger. And the hexagonal Au NPs array films have had stronger Raman-enhanced signal compared to the disorder Au NPs films. Simulations according to the three-dimensional finite-difference time domain (3D-FDTD) have displayed that these electric field enhancements of the ordered hexagonal Au NPs are strongly dependent on the gap distance. Plasmonic ordered hexagonal Au NPs could provide us new platforms to realize novel optoelectronic devices. [ABSTRACT FROM AUTHOR]

We investigate the surface-enhanced Raman spectroscopy of Ag nanorings antenna in both experiment and simulation. Self-organized Ag nanorings antenna were formed on quartz glass wafers by a simple chemistry reaction without any template. The three-dimensional finite-difference time-domain simulation calculations indicate that the electric field enhancement of Ag nanoring antenna is strongly dependent on the gap distance. A very strong surface plasmon coupling in the gap region of Ag nanoring antenna is observed, whose field intensity is enhanced four times compared to that for Ag nanodomes antenna with the same gap distance. Surface-enhanced Raman scattering (SERS) measurements have shown that the SERS intensity acquired from the Ag nanoring antenna is about 16 times stronger than that obtained from Ag nanodomes antenna. These results pave the way to design plasmonic nanostructures for practical applications that require coupled metallic nanoparticles with enhanced electric fields. [ABSTRACT FROM AUTHOR]