中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Identification of FeN4 as an Efficient Active Site for Electrochemical N-2 Reduction

文献类型:期刊论文

作者He, Chao; Wu, Ze-Yuan; Zhao, Lu; Ming, Mei; Zhang, Yun; Yi, Yuanping; Hu, Jin-Song
刊名ACS CATALYSIS
出版日期2019-08-01
卷号9期号:8页码:7311-7317
ISSN号2155-5435
DOI10.1021/acscatal.9b00959
英文摘要Electrocatalytic N-2 reduction to NH3 is an attractive method for artificial N-2 fixation at ambient conditions. Herein, we demonstrate that Fe-NC materials could be efficient for electrochemical N-2 reduction reaction (NRR) using iron phthalocyanine (FePc) with a well-defined FeN4 configuration as a model catalyst. By uniformly loading FePc molecules on porous carbon, it exhibits a high electrocatalytic activity for NRR with a NH3 yield rate of 137.95 mu g h(-1) mg(Fepc)(-1) at a low potential of -0.3 V (vs RHE). Importantly, by making comparisons with phthalocyanine without the Fe center and performing control and poisoning experiments together with theoretical calculations, we identify the Fe center in FeN4 as the most active site for NRR among five possible sites in FePc and discover that the preferred route is the alternating pathway of N-2 on Fe. These results open up opportunities for further exploring metal-nitrogen-carbon materials for highly efficient electrochemical N-2 fixation and NH3 production.
语种英语
WOS记录号WOS:000480503700072
源URL[http://ir.iccas.ac.cn/handle/121111/82695]  
专题中国科学院化学研究所
作者单位Chinese Acad Sci, Inst Chem, Beijing 100190, Peoples R China
推荐引用方式
GB/T 7714
He, Chao,Wu, Ze-Yuan,Zhao, Lu,et al. Identification of FeN4 as an Efficient Active Site for Electrochemical N-2 Reduction[J]. ACS CATALYSIS,2019,9(8):7311-7317.
APA He, Chao.,Wu, Ze-Yuan.,Zhao, Lu.,Ming, Mei.,Zhang, Yun.,...&Hu, Jin-Song.(2019).Identification of FeN4 as an Efficient Active Site for Electrochemical N-2 Reduction.ACS CATALYSIS,9(8),7311-7317.
MLA He, Chao,et al."Identification of FeN4 as an Efficient Active Site for Electrochemical N-2 Reduction".ACS CATALYSIS 9.8(2019):7311-7317.

入库方式: OAI收割

来源:化学研究所

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