N-doped reduced graphene oxide supported Cu2O nanocubes as high active catalyst for CO2 electroreduction to C2H4

被引:76
作者
Ning, Hui [1 ]
Mao, Qinhu [1 ]
Wang, Wenhang [1 ]
Yang, Zhongxue [1 ]
Wang, Xiaoshan [1 ]
Zhao, Qingshan [1 ]
Song, Yan [2 ]
Wu, Mingbo [1 ]
机构
[1] China Univ Petr East China, Inst New Energy, Coll Chem Engn, State Key Lab Heavy Oil Proc, Qingdao 266580, Peoples R China
[2] Chinese Acad Sci, Inst Coal Chem, CAS Key Lab Carbon Mat, Taiyuan 030001, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
N-doped graphene; Cuprous oxide; Electroreduction; Carbon dioxide; Ethylene; CARBON-DIOXIDE; ELECTROCHEMICAL REDUCTION; ETHYLENE; ELECTROCATALYST; NANOPARTICLES; NANOHYBRIDS; TEMPERATURE; PERFORMANCE; SELECTIVITY; SITES;
D O I
10.1016/j.jallcom.2019.01.142
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electrocatalytic carbon dioxide reduction (CO2RR) to high value-added chemicals is a promising technology to address greenhouse effect and energy challenges. As ethylene is a desirable product of CO2RR with great economic value, herein, we proposed a facile method to in situ loading cuprous oxide (Cu2O) nanocubes on nitrogen doped reduced graphene oxide (NRGO) to fabricate a Cu2O/NRGO composite under ambient conditions, which exits a high faradaic efficiency of ethylene (19.7%) at -1.4 V (vs. reversible hydrogen electrode) with stable current density of 12 mA cm(-2). The mass activity of Cu2O supported on NRGO towards C2H4 formation reaches as high as 136.1 mmol h(-1) g(-1), which is more than 24-folds of pristine Cu2O.SEM images reveal that Cu2O with perfect cubic morphology are highly dispersed on NRGO, promoting the exposure of active sites for CO2RR. Additionally, the pyridinic-N in NRGO was supposed to behave synergistic effect with Cu2O, leading to a clearly improvement of activity and durability of Cu2O for electrocatalytic CO2 reduction to ethylene. Our work provides a useful strategy to enhance the catalytic performance of copper catalysts for CO2RR by using nitrogen doped carbon materials as supports. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:7 / 12
页数:6
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