Abstract

We investigate the electronic structure and photoexcitation dynamics of alkali atoms (Rb and Cs) chemisorbed on transition-metal Ru(0001) single-crystal surface by angle- and time-resolved multiphoton photoemission. Three- and four-photon photoemission (3PP and 4PP) spectroscopic features due to the $\ensuremath{\sigma}$ and $\ensuremath{\pi}$ resonances arising from the $ns$ and $np$ states of free alkali atoms are observed from $\ensuremath{\sim}2$ eV below the vacuum level in the zero-coverage limit. As the alkali coverage is increased to a maximum of 0.02 monolayers, the resonances are stabilized by formation of a surface dipole layer, but in contrast to alkali chemisorption on noble metals, both resonances form dispersive bands with nearly free-electron mass. Density functional theory calculations attribute the band formation to substrate-mediated interaction involving hybridization with the unoccupied $d$ bands of the substrate. Time-resolved measurements quantify the phase and population relaxation times in the three-photon photoemission (3PP) process via the $\ensuremath{\sigma}$ and $\ensuremath{\pi}$ resonances. Differences between alkali-atom chemisorption on noble and transition metals are discussed.

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