Surface oxygen Vacancies on Reduced Co3O4(100): Superoxide Formation and Ultra‐Low‐Temperature CO Oxidation

The activation of molecular oxygen is a fundamental step in almost all catalytic oxidation reactions. We have studied this topic and the role of surface vacancies for Co3O4(100) films with a synergistic combination of experimental and theoretical methods. We show that the as‐prepared surface is B‐layer terminated and that mild reduction produces oxygen single and double vacancies in this layer. Oxygen adsorption experiments clearly reveal different superoxide species below room temperature. The superoxide desorbs below ca. 120 K from a vacancy‐free surface and is not active for CO oxidation while superoxide on a surface with oxygen vacancies is stable up to ca. 270 K and can oxidize CO already at the low temperature of 120 K. The vacancies are not refilled by oxygen from the superoxide, which makes them suitable for long‐term operation. Our joint experimental/theoretical effort highlights the relevance of surface vacancies in catalytic oxidation reactions.
Activated molecular oxygen (superoxide, O2 −) can oxidize CO already at 120 K on B‐layer terminated Co3O4(100) with oxygen vacancies. This rendered scheme illustrates how a vibrational spectrum of the adsorbed superoxide is recorded with surface action spectroscopy.