Qian Liang, Jingshan Fan, Jiawen Ding, Xiuzheng Deng, Yingtang Zhou, Jun Cai, Zheng Peng, Zhongyu Li, Zhenhui Kang
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引用次数: 0
Abstract
Regulation of the proton-coupled electron transfer (PCET) process to avoid the unbalanced proton and electron regions on the reduction active sites is key to dictating product selectivity in a photocatalytic CO2 reduction reaction. Here, we show that reversible Mo5+/Mo6+ as a mediator can regulate the proton and electron transfer process at the Bi2MoO6 nanosheet/In2O3 microtube (BI) catalyst. The formed concerted proton-coupled electron transfer enables a champion solar-to-methane efficiency of 0.15%, resulting in nearly 100% CH4 selectivity and a competitive CH4 yield of 46.37 μmol g–1 h–1 in pure water. The experiments, together with theoretical calculations, clearly validate that In sites as H2O oxidation centers provide protons, and the regulation of protons and electrons by using Mo sites forms approximate electroneutral proton/electron pairs, which are conjointly transferred to Bi sites as CO2 adsorption/reduction centers, thus achieving precise hydrogenation on Bi sites for binding of the *CH3O key intermediate to form CH4.
期刊介绍:
ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels.
The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.