Bulk Hydroxylation and Effective Water Splitting by Highly Reduced Cerium Oxide: The Role of O Vacancy Coordination

Reactions of reduced cerium oxide CeOx with water are fundamental processes omnipresent in ceria-based catalysis. Using thin epitaxial films of ordered CeOx, we investigate the influence of oxygen vacancy concentration and coordination on the oxidation of CeOx by water. Upon changing the CeOx stoichiometry from CeO2 to Ce2O3, we observe a transition from a slow surface reaction to a productive H2-evolving CeOx oxidation with reaction yields exceeding the surface capacity and indicating the participation of bulk OH species. Both the experiments and the ab initio calculations associate the effective oxidation of highly reduced CeOx by water to the next-nearest-neighbor oxygen vacancies present in the bixbyite c-Ce2O3 phase. Next-nearest-neighbor oxygen vacancies allow for the effective incorporation of water in the bulk via formation of OH- groups. Our study illustrates that the coordination of oxygen vacancies in CeOx represents an important parameter to be considered in understanding and improving the reactivity of ceria-based catalysts.