TY - JOUR
T1 - Active Sites in Single-Atom Fe-Nx-C Nanosheets for Selective Electrochemical Dechlorination of 1,2-Dichloroethane to Ethylene
AU - Gan, Guoqiang
AU - Li, Xinyong
AU - Wang, Liang
AU - Fan, Shiying
AU - Mu, Jincheng
AU - Wang, Penglei
AU - Chen, Guohua
PY - 2020/8/25
Y1 - 2020/8/25
N2 - 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-Nx-C nanosheet with the presence of a highly efficient Fe-N4 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-N4 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.
AB - 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-Nx-C nanosheet with the presence of a highly efficient Fe-N4 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-N4 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.
KW - active sites
KW - electrocatalytic dechlorination reaction
KW - ethylene production
KW - Fe-Nx-C nanosheet
KW - single-atom catalysts
KW - theoretical calculations
UR - http://www.scopus.com/inward/record.url?scp=85090078731&partnerID=8YFLogxK
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-85090078731&origin=recordpage
U2 - 10.1021/acsnano.0c02783
DO - 10.1021/acsnano.0c02783
M3 - RGC 21 - Publication in refereed journal
C2 - 32672440
SN - 1936-0851
VL - 14
SP - 9929
EP - 9937
JO - ACS Nano
JF - ACS Nano
IS - 8
ER -