Noble- and transition-metal clusters: Thedbands of silver and palladium

Abstract
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 decreasing 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, primarily due to the unit positive charge that remains on the cluster in the photoemission final 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 EF, resulting in a transition to s-electron screening and hence a core-level shift that is larger than the valence-band shift.