Reaction Mechanism Network of CO2 Hydrogenation to Methanol On Cu(111)

Reaction mechanism network of CO₂ hydrogenation to methanol on Cu(111)

Ya-Fan Zhao^1,2, Yong Yang², Charles Mims³, Charles H. F. Peden², Jun Li^1,2,*  and Donghai Mei^2,*

¹Department of Chemistry and Laboratory of Organic Optoelectronics and Molecular Engineering of the Ministry of Education, Tsinghua University, Beijing 100084, China

²Institute for Interfacial Catalysis, Pacific Northwest National Laboratory, Richland WA 99352, USA

³Department of Chemical Engineering and Applied Chemistry, University of Toronto, Ontario, M5S 3E5, Canada   Abstract

Methanol synthesis from CO₂ hydrogenation on supported Cu catalysts is of considerable importance in the chemical and energy industries. Although extensive experimental and theoretical efforts have been carried out in the past decades, the most fundamental questions such as the reaction mechanisms and the key reaction intermediates are still in debate. In the present work, a comprehensive reaction network for CO₂ hydrogenation to methanol on Cu(111) is studied using periodic density functional theory calculations. All of the elementary reaction steps in the reaction network are identified in an unbiased way with the dimer method. Our calculation results show that methanol synthesis from direct hydrogenation of formate on Cu(111) is not feasible due to the high activation barriers for some of the elementary steps. Instead, we find that CO₂ hydrogenation to hydrocarboxyl (trans-COOH) is kinetically more favorable than formate in the presence of H₂O via a unique proton transfer mechanism. The trans-COOH is then converted into hydroxymethylidyne (COH) via dihydroxycarbene (COHOH) intermediates, followed by three consecutive hydrogenation steps to form hydroxymethylene (HCOH), hydroxymethyl (H₂COH), and methanol. This is consistent with recent experimental observations [1], which indicate that direct hydrogenation of formate will not produce methanol under dry hydrogen conditions. Thus, both experiment and computational modeling clearly demonstrate the important role of trace amounts of water in methanol synthesis from CO₂ hydrogenation on Cu catalysts. The proposed methanol synthesis route on Cu(111) not only provides new insights into methanol synthesis chemistry, but also demonstrates again that spectroscopically observed surface species are often not critical reaction intermediates but rather spectator species.