Coadsorption of dioxygen and water on the Ni(110) surface: role of O⁻ -type species in the dissociation of water

Abstract

While the adsorption of dioxygen at a clean Ni(110) surface gives rise to two O(1s) features at 531 and 530 eV assigned to O⁻(a) and O²⁻(a) type species respectively, coadsorption of dioxygen and water mixtures result in the additional formation of hydroxyl species characterized by an O(1s) peak at 532.3 eV. The latter is attributed to the oxygen induced dissociation of water via a low energy pathway involving the O⁻(a)-type species. The proportions of the O⁻(a) and the hydroxyl species are greater for small O₂/H₂O ratios and lower temperatures (120 K). With increase in temperature, the relative surface concentrations of the O⁻(a) and the hydroxyl species decrease while there is an increase in the concentration of the oxidic O²⁻(a) species. Thus, the surface concentrations of both the hydroxyl and the O²⁻(a) species depend critically on the presence of O⁻ type species. Above 300K the surface chemistry in the main involves the conversion of O⁻ to O²⁻ species via the hydroxyl species.