期刊
ACS CATALYSIS
卷 -, 期 -, 页码 -出版社
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.3c03431
关键词
CO2 hydrogenation; methanol synthesis; Cu; size effect; synergism
CuGaZrOx solid solution catalysts show promise for the selective hydrogenation of CO2 to methanol. The structural complexity of the catalyst presents a challenge to understanding the nature of active sites. This study reveals that synergistic interactions between copper and gallium species enhance the capacity for CO2 adsorption/activation and promote the hydrogenation of CO2 to form methanol via a formate pathway.
A Cu-based catalyst has prospects for practical use in selective hydrogenation of CO2 to methanol. But the catalyst's structural complexity renders the elucidation of the nature of active sites a challenge. This work reports CuGaZrOx solid solutions with tunable Cu size scales and synergetic interactions between active sites for methanol synthesis. Atomically dispersed Cu species (Cu-1-O-3) adjacent to the Zr site contribute to enhanced capacity for CO2 adsorption/activation, and Ga sites are primarily responsible for H-2 dissociation over the CuGaZrOx solid solution with isolated Cu species. Further experimental and density functional theory (DFT) calculations reveal that the synergy between Cu and Ga species favors the hydrogenation of CO2 to form CH3OH via a formate pathway while suppressing undesired CO production. This work provides insight into the active site structure and mechanistic pathway over a CuGaZrOx solid solution and efficient catalyst design for CO2 hydrogenation to methanol.
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