This paper describes methodologies for fabricating of highly efficient plasmonics-active SERS substrates -having metallic nanowire structures with pointed geometries and sub-5 nm gap between the metallic nanowires enabling concentration of high EM fields in these regions -on a wafer-scale by a reproducible process that is compatible with large-scale development of these substrates. Excitation of surface plasmons in these nanowire structures leads to substantial enhancement in the Raman scattering signal obtained from molecules lying in the vicinity of the nanostructure surface. The methodologies employed included metallic coating of silicon nanowires fabricated by employing deep UV lithography as well as controlled growth of silicon germanium on silicon nanostructures to form diamond-shaped nanowire structures followed by metallic coating. These SERS substrates were employed for detecting chemical and biological molecules of interest. In order to characterize the SERS substrates developed in this work, we obtained SERS signals from molecules such as p-mercaptobenzoic acid (pMBA) and cresyl fast violet (CFV) attached to or adsorbed on the metal-coated SERS substrates. It was observed that both gold-coated triangular shaped nanowire substrates as well as gold-coated diamond shaped nanowire substrates provided very high SERS signals for the nanowires having sub-15 nm gaps and that the SERS signal depends on the closest spacing between the metal-coated silicon and silicon germanium nanowires. SERS substrates developed by the different processes were also employed for detection of biological molecules such as DPA (Dipicolinic Acid), an excellent marker for spores of bacteria such as Anthrax.
IntroductionIn recent years, there has been extensive research aimed at developing plasmonics-active substrates that generate high surface enhanced Raman scattering (SERS) signals resulting in high sensitivities and specificities towards chemical and biological molecules adsorbed on the substrates 1-20 . The advantage of employing SERS as a sensing platform is that SERS spectra exhibit narrow spectral features characteristic of the detected analyte species which allows label-free and specific detection of these species in the presence of multiple other molecules in complex mixtures. Raman scattering can be described as an inelastic light scattering process in which a target sample on which light is incident absorbs one photon and emits another photon at the same time, the second photon being either at a lower frequency (i.e. Stokes scattering) or at a higher frequency (i.e. Anti-Stokes scattering) than the incident light frequency. While Raman scattering cross-sections are extremely small -typically between 10 -30 to 10 -25 cm 2 per molecule -thereby limiting its ability to detect the analyte species, Surface enhanced Raman scattering (SERS) increases the Raman scattering cross-section substantially enabling the application of this process for extremely sensitive and specific detection of the analytes 1-3 . Reports on the large SE...