Elucidating the Nature of the Cu(I) Active Site in CuO/TiO2 for Excellent Low-Temperature CO Oxidation

ACS Appl Mater Interfaces. 2020 Feb 12;12(6):7091-7101. doi: 10.1021/acsami.9b18264. Epub 2020 Feb 3.

Abstract

Stabilized Cu+ species have been widely considered as catalytic active sites in composite copper catalysts for catalytic reactions with industrial importance. However, few examples comprehensively explicated the origin of stabilized Cu+ in a low-cost and widely investigated CuO/TiO2 system. In this study, mass producible CuO/TiO2 catalysts with interface-stabilized Cu+ were prepared, which showed excellent low-temperature CO oxidation activity. A thorough characterization and theoretical calculations proved that the strong charge-transfer effect and Ti-O-Cu hybridization in Ti-doped CuO(111) at the CuO/TiO2 interface contributed to the formation and stabilization of Cu+ species. The CO molecule adsorbed on Cu+ and reacted directly with Ti doping-promoted active lattice oxygen via a Mars-van Krevelen mechanism, leading to the enhanced low-temperature activity.

Keywords: CO adsorption; Ti-doped CuO; Ti−O−Cu hybridization; activated O; stabilized Cu+.