Optical Activity of Metal Nanoclusters Deposited on Regular and Doped Oxide Supports from First-Principles Simulations

We report a computational study and analysis of the optical absorption processes of Ag-20 and Au-20 clusters deposited on the magnesium oxide (100) facet, both regular and including point defects. Ag-20 and Au-20 are taken as models of metal nanoparticles and their plasmonic response, MgO as a model of a simple oxide support. We consider oxide defects both on the oxygen anion framework (i.e., a neutral oxygen vacancy) and in the magnesium cation framework (i.e., replacing Mg++ with a transition metal: Cu++ or Co++). We relax the clusters' geometries via Density-Functional Theory (DFT) and calculate the photo-absorption spectra via Time-Dependent DFT (TDDFT) simulations on the relaxed geometries. We find that the substrate/cluster interaction induces a broadening and a red-shift of the excited states of the clusters, phenomena that are enhanced by the presence of an oxygen vacancy and its localized excitations. The presence of a transition-metal dopant does not qualitatively affect the spectral profile. However, when it lies next to an oxygen vacancy for Ag-20, it can strongly enhance the component of the cluster excitations perpendicular to the surface, thus favoring charge injection.

Automated summary

A computational study was conducted on the optical absorption processes of Ag-20 and Au-20 clusters on the magnesium oxide (100) facet, with regular and point defect configurations. The interaction between the substrate and clusters induced broadening and red-shift of the excited states, which were further enhanced by the presence of oxygen vacancies.