催化作用
电化学
一氧化碳
法拉第效率
氮气
碳纤维
氧化还原
无机化学
材料科学
金属
化学
电极
有机化学
冶金
物理化学
复合材料
复合数
作者
Xiang Lyu,Dimitra Maria Anastasiadou,Jithu Raj,Jingjie Wu,Yaocai Bai,Jianlin Li,David A. Cullen,Jun Yang,Liliana P. L. Gonçalves,Oleg I. Lebedev,Yury V. Kolen’ko,Marta Costa Figueiredo,Alexey Serov
标识
DOI:10.1016/j.electacta.2023.142427
摘要
Here, we report a facile approach for synthesizing M–N–C catalysts (M = Co, Fe, Ni) at a commercial scale without employing organic solvents. Our characterization efforts indicate that single atomic catalysts with high surface areas were successfully obtained. Electrochemical measurements demonstrate that, among the three synthesized catalysts, Ni–N–C exhibits the highest performance in the electrochemical CO2 reduction reaction (CO2RR) to carbon monoxide (CO), affording 80% Faradaic efficiency (FE) of CO production at –0.49 VRHE with a turnover frequency (TOF) of 57,379 h–1. Large-scale synthesis coupled with high performance allows moving forward with the practical implementation of M–N–C catalysts for industrially relevant CO2RR.
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