Substrates based on the metal-polymer nanocomposites 2,3-dichloro-p-xylylene-silver (PCPX-Ag) that realize the effect of surface-enhanced Raman scattering (SERS) were developed. To obtain nanocomposites, the vapor-phase polymerization method was used (VDP), which makes it possible to control the nanocomposite microstructure. In the process of self-assembly during VDP, nanocomposite films with inclusions of silver particles were formed on the polycore substrates. Silver content varied from 2.5 to 16% vol. The possibility of using such substrates for the detection of low-molecular substances, for example 5,5′-dithiobis- (2-nitrobenzoic acid) (DTNB) analyte, by the SERS method with an enhancement factor of up to 104, was demonstrated. The dependence of the SERS spectra enhancement on the microstructure of the nanocomposite and the silver content was determined. The optical and morphological properties of nanocomposites were also investigated and their dependence on the silver content was shown. It has been demonstrated that the nanocomposite is SERS selective since when working with complex solutions in the presence of high molecular weight substances, signal enhancement was only observed for low molecular weight substances.
Spectroscopy based on surface enhanced Raman scattering (SERS) is widely used as a method with extremely high sensitivity for molecular and chemical analysis. We have developed thin-film sandwich structures, in which, when used as sensitive elements for detecting organic compounds at low concentrations, high-amplitude spectra of surface enhanced Raman scattering are observed. Using gas-phase cryochemical synthesis and thermal sputtering in vacuum, SERS active sandwich structures Ag–poly(chloro-p-xylylene)–Ag (Ag–PCPX–Ag) were obtained. In the process of creating sandwich structures, the upper silver film takes the form of a complex island topology with submicron sizes. A series of samples were made with different thicknesses of the polymer and upper silver layers. SERS spectra of the analyte chemically adsorbed on the film surface were obtained, demonstrating a significant amplification (up to 104) compared with the control sample. The dependence of the gain on the silver concentration is characterized by a maximum polymer layer thickness of 600 nm and a 30 nm thick upper silver layer. A selective amplification of the low molecular weight compound spectra with respect to proteins was observed. A semi-empirical model is proposed that is in good agreement with the experimental results.
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