Surface-enhanced Raman scattering of perchlorate on cationic-modified silver nanofilms - Effect of inorganic anions

Surface-enhanced Raman scattering (SERS) has emerged as one of the most sensitive spectroscopic analysis methods for the detection of environmental contaminants in water, including perchlorate (ClO4(-)). However, as with other commonly used analytical techniques, analysis of realistic environmental samples by SERS presents a challenge due to complex chemical components coexisting in the samples. In this work, we investigated the influence of inorganic anions (particularly oxyanions) on SERS spectra of ClO4(-) using a cationic thiol modified silver nanofilm substrate (Cys-Ag/rCu). The results show that the anions present in the samples did not shift the ClO4(-) characteristic band positions, but did decrease signal intensities due to their competitive binding with the -NH3(+) groups of cationic thiol molecules immobilized on the substrates. The pH changes caused by both the dissociation of H2PO4(-) and the hydrolysis of HCO3(-) may also play a non-negligible role. The selectivity of the Cys-Ag/rCu substrate towards these anions was determined to be in the following order: ClO4(-)>SO4(2-)>HCO3(-), NO3(-)>Cl(-)>H2PO4(-), indicating preferential adsorption of ClO4(-) ions. In the solutions with multiple anions present, the ClO4(-) SERS spectra were affected simultaneously by all the coexisting anions. Calibration curves with very good linear relationships were successfully obtained, demonstrating the great potential of quantitative detection of aqueous ClO4(-) in the matrix.