法拉第效率
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
无机化学
化学
电极
物理化学
有机化学
参比电极
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
Abstract The electrochemical CO 2 reduction reaction (CO 2 RR) to give C 1 (formate and CO) products is one of the most techno‐economically achievable strategies for alleviating CO 2 emissions. Now, it is demonstrated that the SnO x shell in Sn 2.7 Cu catalyst with a hierarchical Sn‐Cu core can be reconstructed in situ under cathodic potentials of CO 2 RR. The resulting Sn 2.7 Cu catalyst achieves a high current density of 406.7±14.4 mA cm −2 with C 1 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 C 1 Faradaic efficiency of 99.0±0.5 % for 40 h at −0.55 V vs. RHE. DFT calculations indicate that the reconstructed Sn/SnO x interface facilitates formic acid production by optimizing binding of the reaction intermediate HCOO* while promotes Faradaic efficiency of C 1 products by suppressing the competitive hydrogen evolution reaction, resulting in high Faradaic efficiency, current density, and stability of CO 2 RR at low overpotentials.
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