Abstract
Enhanced second-order Raman modes of C60 molecules adsorbed on Ag and In surfaces are reported. This unusual observation for the metal surfaces is believed to result from the unique surface-enhancement mechanism of the Raman spectrum of adsorbed C60 and from the high relative intensity of the second-order modes previously observed for bulk C60 samples. Differences in line shapes and a modified resonant behavior, relative to results for C60 single crystals, are attributed to interactions between the adsorbed C60 and the metal surfaces, which have been shown in previous studies to include charge transfer to C60.