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Chemical enhancement of surface-enhanced Raman spectroscopy was investigated using a gold nanoparticle (AuNP)-coated polymer substrate, and an enormous b 2 -mode signal enhancement arose from the evaporation-induced reorientation of 4-aminobenzenethiol molecules adsorbed onto the AuNP surface. The dynamic analysis of time-dependent increases of chemically enhanced Raman signals enables us to measure the charge coupling strengths between molecules and metal at varying surface environments and to differentiate the solvent drying-mediated coupling effect with a long-term stability from photogenerated, metastable charged states showing a relatively rapid signal decay.
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Nam‐Jung Kim (2010) studied this question.
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