Active Sites in Single-Atom Fe-Nx-C Nanosheets for Selective Electrochemical Dechlorination of 1,2-Dichloroethane to Ethylene

被引:107
作者
Gan, Guoqiang [1 ]
Li, Xinyong [1 ]
Wang, Liang [1 ]
Fan, Shiying [1 ]
Mu, Jincheng [1 ]
Wang, Penglei [1 ]
Chen, Guohua [2 ]
机构
[1] Dalian Univ Technol, Sch Environm Sci & Technol, State Key Lab Fine Chem, Key Lab Ind Ecol & Environm Engn MOE, Dalian 116024, Peoples R China
[2] Hong Kong Polytech Univ, Dept Mech Engn, Kowloon, Hong Kong SAR, Peoples R China
基金
中国国家自然科学基金;
关键词
single-atom catalysts; Fe-N-x-C nanosheet; electrocatalytic dechlorination reaction; ethylene production; theoretical calculations; active sites; OXYGEN REDUCTION; IRON; CATALYSTS; CARBON; IDENTIFICATION;
D O I
10.1021/acsnano.0c02783
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrochemical dechlorination of 1,2-dichloroethane (DCE) is one of the prospective and economic strategies for the preparation of high-value ethylene. However, the exploration of advanced electrocatalysts with high reactivity and selectivity and the identification of their active sites are still a challenge. Herein, a single-atom (SA) Fe-N-x-C nanosheet with the presence of a highly efficient Fe-N-4 coordination pattern is reported. The as-prepared single-atom electrocatalyst exhibits a higher reactivity and ethylene selectivity for DCE dechlorination reaction than those of the commercially adopted 20% Pt-C catalyst. By a combination of experiments and theoretical calculations, the atomically dispersed Fe center in the Fe-N-4 structure was unveiled to be the dominating active site for electrochemical production of ethylene. Our work would offer an approach for the rational development of SA materials and supply crucial insight into the mechanism of ethylene production through the DCE dechlorination reaction.
引用
收藏
页码:9929 / 9937
页数:9
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