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10 October 2007The role of surface adsorption in surface-enhanced Raman scattering from Benzene thiols
The origins of the surface-enhanced Raman (SERS) effect have been widely studied and are generally accepted as
understood. However, there is still a need to provide a satisfactorily complete model which addresses the well known
phenomena in which some molecules exhibit weak or even no SERS response at all. The relative intensities of
vibrational modes observed in SERS can depend strongly on the mechanism of surface adsorption, such as bond type
(covalent/noncovalent) and number of covalent bonds. Thus, in this experimental study the role of surface adsorption in
surface-enhanced Raman scattering is investigated. A simple group of Benzene thiols was chosen to facilitate
comparison with theoretical models. Experimental results with consideration towards surface bond strengths and
reduction in degrees of freedom due to single and multiple surface bonds is presented and their effect on the relative
intensities and positions of observed vibrational modes observed in the SERS spectra are discussed. The relative
stability of molecules in the presence of nanostructures exhibiting strong and weak local electric fields will also be
presented and discussed.
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D. A. Alexson, O. J. Glembocki, S. M. Prokes, R. W. Rendell, S. C. Badescu, J. Onuegbu, C. M. Hosten, "The role of surface adsorption in surface-enhanced Raman scattering from Benzene thiols," Proc. SPIE 6768, Nanomaterials Synthesis, Interfacing, and Integrating in Devices, Circuits, and Systems II, 67680S (10 October 2007); https://doi.org/10.1117/12.752592