Hydride Generation on the Cu-Doped CeO2(111) Surface and Its Role in CO2 Hydrogenation Reactions

Abstract

Ceria-based catalysts exhibit great activity in catalyzing selective hydrogenation of CO2 to methanol. However, the underlying mechanism of this reaction, especially the generation of active H species, remains unclear. In this work, we performed extensive density functional theory calculations corrected by on-site Coulomb interaction (DFT + U) to investigate the H2 dissociation and the reaction between the active H species and CO2 on the pristine and Cu-doped CeO2(111) (denoted as Cu/CeO2(111)) surfaces. Our calculations evidenced that the heterolytic H2 dissociation for hydride generation can more readily occur on the Cu/CeO2(111) surface than on the pristine CeO2(111) surface. We also found that the Cu dopant can facilitate the formation of surface oxygen vacancies, further promoting the generation of hydride species. Moreover, the adsorption of CO2 and the hydrogenation of CO2 to HCOO* can be greatly promoted on the Cu/CeO2(111) surface with hydride species, which can lead to the high activity and selectivity toward CO2 hydrogenation to methanol.