LAUSR

Abstract Density functional theory (DFT) based calculations are carried out to study effect of molecular charge on both the binding energy as well as chemical Raman enhancement of deprotonated 4-Mercaptopyridine (ligand) bound to the semiconducting nanocluster, Zn3Se3 and metal substituted nanoclusters, Zn2MSe3 (M: Ag, Cu). Change of molecular charge from 0 to −1 increases binding energy of the ligand for Zn3Se3 cluster and decreases Raman activity of vibrational modes. On the other hand, the ligand bound to the metal substituted nanoclusters, Zn2MSe3 shows minimal decrease in binding energy and a noteworthy enhancement in Raman activity of the vibrational modes, on varying the molecular charge from 0 to −1. Static Raman activities of vibrational modes are analyzed using change of molecular polarizability components with normal coordinates of the modes. An APT (Atomic Polar Tensor) charge based descriptor is used for characterization of the chemical Raman enhancement. The descriptor measures substrate induced charge concentration per unit displacement of an atom involved in a mode of vibration. We also show that significantly enhanced intensity of vibrational modes is associated with atoms of relatively greater magnitudes of the APT charge based descriptor.