法拉第效率
SN2反应
催化作用
格式化
电化学
甲酸
可逆氢电极
材料科学
氧化还原
锡
无机化学
化学工程
化学
电极
物理化学
立体化学
有机化学
工作电极
冶金
工程类
作者
Ke Ye,Zhiwen Zhou,Jiaqi Shao,Long Lin,Dunfeng Gao,Na Ta,Rui Si,Guoxiong Wang,Xinhe Bao
标识
DOI:10.1002/anie.201916538
摘要
The electrochemical CO2 reduction reaction (CO2 RR) to give C1 (formate and CO) products is one of the most techno-economically achievable strategies for alleviating CO2 emissions. Now, it is demonstrated that the SnOx shell in Sn2.7 Cu catalyst with a hierarchical Sn-Cu core can be reconstructed in situ under cathodic potentials of CO2 RR. The resulting Sn2.7 Cu catalyst achieves a high current density of 406.7±14.4 mA cm-2 with C1 Faradaic efficiency of 98.0±0.9 % at -0.70 V vs. RHE, and remains stable at 243.1±19.2 mA cm-2 with a C1 Faradaic efficiency of 99.0±0.5 % for 40 h at -0.55 V vs. RHE. DFT calculations indicate that the reconstructed Sn/SnOx interface facilitates formic acid production by optimizing binding of the reaction intermediate HCOO* while promotes Faradaic efficiency of C1 products by suppressing the competitive hydrogen evolution reaction, resulting in high Faradaic efficiency, current density, and stability of CO2 RR at low overpotentials.
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