SURFACE-ENHANCED RAMAN SPECTRAL STUDY OF AU NANO-PARTICLES/ ALKANETHIOL SELF-ASSEMBLED MONOLAYERS/AU (1 1 1) HETEROSTRUCTURES

Abstract This paper describes Raman spectroscopic investigations of octadecane–thiol (C 18 H 37 –SH; OD–mT) and octane–dithiol (HS–C 8 H 16 –SH; O–dT) self-assembled monolayers (SAMs) on an epitaxial Au(1 1 1 )/cleaved-mica substrate. The epitaxial Au(1 1 1 ) substrate having nanometer-scale domains increases the enhanced Raman signals of SAMs, whereas the Raman bands are much less intense on the micrometer-scale domains of Au(1 1 1 ). The Raman intensity of the ν s (CH 2 ) band is increased for depositions above 4 nm, and takes a maximum at a thickness of 9 nm when gold is vacuum-deposited on the OD–mT SAMs that are formed on micrometer-scale domains. For the O–dT SAMs, Raman band intensity profiles show two features at gold thicknesses of 2 and 9 nm; the latter intensity is about three times greater than that of the former. Atomic force microprobe (AFM) images reveal that 20–30-nanometer-scale islands are formed by 9 nm gold deposition for both SAMs. In contrast, 2 nm gold deposition onto the O–dT SAMs creates striped nanostructures (ca. 7 nm in spacing). The results suggest that the specific nanostructures formed by post-deposition of gold serve to enhance the SAMs Raman signals.