催化作用
一氧化碳
二氧化碳电化学还原
活性炭
二氧化碳
无机化学
材料科学
等离子体
甲烷化器
化学
化学工程
有机化学
吸附
量子力学
物理
工程类
作者
Hemma Mistry,Yong‐Wook Choi,Alexander Bagger,Fabian Scholten,Cecile S. Bonifacio,Ilya Sinev,Núria J. Divins,Ioannis Zegkinoglou,Hyo Sang Jeon,Kim Kisslinger,Eric A. Stach,Judith C. Yang,Jan Rossmeisl,Beatriz Roldán Cuenya
标识
DOI:10.1002/anie.201704613
摘要
Abstract Efficient, stable catalysts with high selectivity for a single product are essential if electroreduction of CO 2 is to become a viable route to the synthesis of industrial feedstocks and fuels. A plasma oxidation pre‐treatment of silver foil enhances the number of low‐coordinated catalytically active sites, which dramatically lowers the overpotential and increases the activity of CO 2 electroreduction to CO. At −0.6 V versus RHE more than 90 % Faradaic efficiency towards CO was achieved on a pre‐oxidized silver foil. While transmission electron microscopy (TEM) and operando X‐ray absorption spectroscopy showed that oxygen species can survive in the bulk of the catalyst during the reaction, quasi in situ X‐ray photoelectron spectroscopy showed that the surface is metallic under reaction conditions. DFT calculations reveal that the defect‐rich surface of the plasma‐oxidized silver foils in the presence of local electric fields drastically decrease the overpotential of CO 2 electroreduction.
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