甲烷
催化作用
选择性
材料科学
兴奋剂
氧化还原
法拉第效率
氢
电化学
电解质
化学
化学工程
无机化学
电极
物理化学
有机化学
光电子学
工程类
作者
Armin Sedighian Rasouli,Xue Wang,Joshua Wicks,Cao‐Thang Dinh,Jehad Abed,Fang–Jing Wu,Sung‐Fu Hung,Koen Bertens,Jianan Erick Huang,Edward H. Sargent
出处
期刊:Chem catalysis
[Elsevier]
日期:2022-04-01
卷期号:2 (4): 908-916
被引量:17
标识
DOI:10.1016/j.checat.2022.03.016
摘要
The electrochemical CO2 reduction reaction (CO2RR) provides a route to store intermittent electricity in the form of fuels like methane. We reasoned that disrupting C-C coupling while maintaining high ∗CO coverage could enhance methane selectivity and suppress the hydrogen evolution reaction (HER). We studied the effect of doping CuAl, a material at the top of the CO2RR activity and selectivity volcano plot, with elements having low ∗CO binding energies: Au, Zn, and Ga. Encouraged by initial improvements in selectivity to methane, we optimized the Ga content and showed that the presence of uniformly dispersed Ga is crucial in CO2RR-to-methane performance enhancement. We rule out porosity and roughness and conclude that the presence of Ga in the doped catalysts enables high methane selectivity. The Ga-doped CuAl catalysts achieve a methane Faradaic efficiency (FE) of 53% by suppressing HER to 23% in neutral electrolyte at −1.4 V versus reversible hydrogen electrode.
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