We investigated the mechanisms underlying strong metal-support interactions in CO oxidation using model systems where noble metal crystals support reducible, monolayer-thick CoOx films. The effect of the Co oxidation state, film thickness, and substrate identity were studied in varying reaction conditions using ambient pressure X-ray photoelectron spectroscopy. At low O2 pressures, the same oxide phase forms on both Pt(111) and Au(111) surfaces. But when heated at higher O2 pressures, the oxide phase depends on the substrate. We found that CoOx/Pt is more active for the CO oxidation reaction than CoOx/Au, even when both surfaces stabilize the same oxide phase. DFT calculations on these and related noble-metal-supported CoOx films reveal an SMSI-induced reactivity enhancement that strongly depends on the oxide film thickness and which is mediated by charge transfer between the metal and oxide. Charge transfer is also found to correlate with the reaction energy and activation barrier for CO oxidation. This effect was found to be greatest for oxide films on Pt, decreasing on other noble metal supports in the order Pt > Pd > Au > Ag, in agreement with the experiments. The role of charge transfer in the activation barriers and reaction energies provides insight into the nature of SMSI-induced catalytic activity, and suggests that the noble metal work function can serve as an indicator for the strength of SMSI effects.
Yan et al. (2026) studied this question.