The cobalt oxidation state in preferential CO oxidation on CoOx/Pt(111) investigated by operando X-ray photoemission spectroscopy

Abstract

The combination of a reducible transition metal oxide and a noble metal such as Pt often leads to active low-temperature catalysts for the preferential oxidation of CO in excess H₂ gas (PROX reaction). While CO oxidation has been investigated for such systems in model studies, the added influence of hydrogen gas, representative of PROX, remains less explored. Herein, we use ambient pressure scanning tunneling microscopy and ambient pressure X-ray photoelectron spectroscopy on a CoO_x/Pt(111) planar model catalyst to analyze the active phase and the adsorbed species at the CoO_x/Pt(111) interface under atmospheres of CO and O₂ with a varying partial pressure of H₂ gas. By following the evolution of the Co oxidation state as the catalyst is brought to a reaction temperature of above 150 °C, we determine that the active state is characterized by the transformation from planar CoO with Co in the 2+ state to a mixed Co²⁺/Co³⁺ phase at the temperature where CO₂ production is first observed. Furthermore, our spectroscopy observations of the surface species suggest a reaction pathway for CO oxidation, proceeding from CO exclusively adsorbed on Co²⁺ sites reacting with the lattice O from the oxide. Under steady state CO oxidation conditions (CO/O₂), the mixed oxide phase is replenished from oxygen incorporating into cobalt oxide nanoislands. In CO/O₂/H₂, however, the onset of the active Co²⁺/Co³⁺ phase formation is surprisingly sensitive to the H₂ pressure, which we explain by the formation of several possible hydroxylated intermediate phases that expose both Co²⁺ and Co³⁺. This variation, however, has no influence on the temperature where CO oxidation is observed. Our study points to the general importance of a dynamic reducibility window of cobalt oxide, which is influenced by hydroxylation, and the bonding strength of CO to the reduced oxide phase as important parameters for the activity of the system.