过电位
格式化
法拉第效率
X射线光电子能谱
拉曼光谱
催化作用
硫化物
材料科学
二氧化碳电化学还原
电化学
无机化学
化学工程
化学
电极
一氧化碳
冶金
物理化学
有机化学
物理
光学
工程类
作者
Siting Cai,Mengdi Wang,Bin Chen,Xin Xu,Linhua Mi,Borong Li,Chengkai Yang,Liuyi Li,Shenghong Zhong,Yan Yu
标识
DOI:10.1016/j.ceja.2022.100383
摘要
Transformation of carbon dioxide to useful fuels or chemicals is desirable to build up a sustainable society. In this study, we demonstrate that Cu2S has great potential for electrochemical CO2 reduction. They enable the selective CO2 reduction to formate starting at a low overpotential (∼ 120 mV), with high current density (over -20 mA/cm2 at -0.89 VRHE), and good Faradaic efficiency (>75%) over a broad potential window (-0.7 VRHE to -0.9 VRHE). X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and in-situ Raman spectroscopy studies reveal that Cu2S catalysts are electrochemically stable under the reaction conditions. Further-more, Cu2S catalysts show excellent durability without deactivation following more than 15 cycles (1.0 h per cycle) of operation.
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