Abstract
The adsorption and dissociation of methanol on the fully oxidized and partially reduced (111) cerium oxide surface is studied using the PW91 functional as well as the PW91+U scheme. We investigate the influence of the detailed electronic structure of the Ce 4f band on the chemistry of methanol on the surface. For the partially reduced surface we obtain a spin delocalized, a ferromagnetic, and an anti-ferromagnetic solution. We find that the qualitative conclusions are independent of the surface type used. Methanol adsorption is exothermic on the fully oxidized as well as on the partially reduced surface. Also dissociation of methanol on the surface is exothermic but strongly enhanced by the presence of a vacancy. We localize an on-top methoxy species as a dissociation product on the fully oxidized surface and a triply bridged methoxy species on the partially reduced surface where the methoxy oxygen partly fills the oxygen vacancy in the surface. Adsorption energies are influenced by the introduction of the repulsive Hubbard (U) term. On the other hand, relative surface stabilities like dissociation energies are less sensitive.