Fe, Mo N/C Hollow Porous Nitrogen-Doped Carbon Nanorods as an Effective Electrocatalyst for N2 Reduction Reaction

被引:83
|
作者
Ye, Wen [1 ]
Yang, Yongsheng [2 ]
Arif, Muhammad [3 ]
Yang, Shiyu [3 ]
Fang, Xiaoyu [3 ]
Mushtaq, Muhammad Asim [3 ]
Chen, Xuebo [3 ,4 ]
Yan, Dongpeng [3 ,4 ,5 ]
机构
[1] Univ Sci & Technol Beijing, Inst Solid State Chem, Dept Phys Chem, Beijing Adv Innovat Ctr Mat Genome Engn,Basic Exp, Beijing 100083, Peoples R China
[2] Shenyang Normal Univ, Inst Catalysis Energy & Environm, Coll Chem & Chem Engn, Shenyang 110034, Peoples R China
[3] Beijing Normal Univ, Coll Chem, Beijing Key Lab Energy Convers & Storage Mat, Beijing 100875, Peoples R China
[4] Zhengzhou Univ, Coll Chem & Mol Engn, Zhengzhou 450001, Peoples R China
[5] Changzhou Univ, Jiangsu Key Lab Adv Catalyt Mat & Technol, Changzhou 213164, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
N-2 reduction reaction; electrocatalyst; ammonia production; Faradaic efficiency; Fe; Mo-N/C hollow nanorods; AMMONIA-SYNTHESIS; EFFICIENT ELECTROCATALYST; AMBIENT CONDITIONS; OXYGEN; ELECTROLYSIS; FRAMEWORKS; NANOSHEETS; CATALYSTS; HYBRID; ARRAY;
D O I
10.1021/acssuschemeng.0c05523
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of highly active, non-noble metal-based materials for electrocatalytic nitrogen reduction reaction (NRR) under environmental conditions is still a challenge. Herein, we have designed novel Fe, MoN/C hollow porous nitrogen-doped carbon nanorods as an effective catalyst for N-2 fixation by means of the pyrolysisacid etching process. A high ammonia (NH3) formation rate (1.52 x 10(6) mol h(1) cm(2)) and Faradaic efficiency (FE, 14.2%) at -0.1 V versus RHE are obtained for NRR in 0.1 M Na2SO4 solution. FeN chi and MoN chi units simultaneously serve as catalytic sites for promoting ammonia synthesis, and the concentration of pyridinic N is also essential for the enhanced ammonia production and FE. Therefore, this study accomplishes superior electrocatalytic performance of the Fe, MoN/C hollow nanorods toward NRR in ammonia synthesis application.
引用
收藏
页码:15946 / 15952
页数:7
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