Hydrogenation of CO2 to Methanol on CeOx/Cu(111) and ZnO/Cu(111) Catalysts: Role of the Metal-Oxide Interface and Importance of Ce3+ Sites

摘要

The role of the interface between a metal and oxide (CeOx-Cu and ZnO-Cu) is critical to the production of methanol through the hydrogenation of CO2 (CO2 + 3H(2) -> CH3OH + H2O). The deposition of nanoparticles of CeOx or ZnO on Cu(111), theta(oxi) < 0.3 monolayer, produces highly active catalysts for methanol synthesis. The catalytic activity of these systems increases in the sequence: Cu(111) < ZnO/Cu(111) < CeOx/Cu(111). The apparent activation energy for the CO2 CH3OH conversion decreases from 25 kcal/mol on Cu(111) to 16 kcal/mol on ZnO/Cu(111) and 13 kcal/mol on CeOx/Cu(111). The surface chemistry of the highly active CeOx-Cu(111) interface was investigated using ambient pressure X-ray photoemission spectroscopy (AP-XPS) and infrared reflection absorption spectroscopy (AP-IRRAS). Both techniques point to the formation of formates (HCOO) and carboxylates (CO2 delta-) during the reaction. Our results show an active state of the catalyst rich in Ce3+ sites which stabilize a CO2 delta- species that is an essential intermediate for the production of methanol. The inverse oxide/metal configuration favors strong metaloxide interactions and makes possible reaction channels not seen in conventional metal/oxide catalysts.