Abstract
Surface-enhanced Raman spectroscopy is a powerful analytical method, and is especially useful for the detection of nitrogen- and sulfur-containing organic substances in trace amounts. SERS substrates with high enhancement factors can be produced via the aggregation of gold nanoparticles, leading to the formation of ‘hot spots’ – regions of highest electric field intensity and Raman scattering enhancement. Thus, the availability of gold surfaces in ‘hot spots’ for the adsorption of analyte molecules strongly influences the enhancement factor of a substrate. We studied the kinetics of oxidation of dyes with hydrogen peroxide in the presence of citrate-capped gold nanoparticles and discovered the amplification of surface-enhanced Raman scattering, probably due to the oxidation of citrate ligands and the additional adsorption of dye molecules onto vacant spots on the gold surface. Maximum amplification was observed with 3% (v/v) hydrogen peroxide in the reaction medium. Under optimized conditions, model analytes can be detected at concentrations as low as 1 × 10−9 M, which is ten times lower than the detection limit without hydrogen peroxide addition.
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