Hydrogen adsorption energies on bimetallic overlayer systems at the solid-vacuum and the solid-liquid interface

Atomic hydrogen adsorption energies on bimetallic overlayer systems have been determined by periodic density functional theory calculations within the generalized gradient approximation. On the pseudomorphic Pd/Cu(111) surface, both the substrate interaction and the lattice compression of the Pd overlayer lead to smaller hydrogen binding energies. For pseudomorphic Cu/Pd(111), on the hand, the strong Cu-Pd interaction results in larger binding energies. Hence, both Pd/Cu(111) and Cu/Pd(111) exhibit an intermediate behavior between pure Cu(111) and pure Pd(111). In addition, we have determined the atomic hydrogen adsorption on Pd/Au(111) in the presence of a water overlayer. The hydrogen adsorption energies are changed by less than 60 meV by the most stable H2O bilayer compared to the clean surface. This indicates that theoretical adsorption studies at the solid-vacuum interface might also be relevant for the solid-liquid interface.