Noble and Transition Metal Clusters: The d-bands of silver and palladium.

A comparison of X-ray photoemission from Ag and Pd clusters grown on amorphous carbon substrates highlights the importance of the unfilled 4d band in Pd clusters. In both cases, the valence band spectra show the d-band narrowing with deceasing cluster size, as expected. In both cases, also, there is a positive shift of the binding energies of the d-band centroids and of the core levels, due primarily to the unit positive charge that remains on the cluster in the photoemission finale state, as occurs for other metal clusters on amorphous carbon. In Ag clusters, the core level shift is smaller than the valence band shift because in small clusters the coulomb energy of the charged cluster suppresses the conduction electron screening of the core hole. By contrast, in Pd clusters the increased localization causes a reduction in the d electron density of states at E(F), resulting in a transition to s-electron screening and hence a core level shift that is larger than the valence band shift.