Recent Progress in Electrochemical Nitrogen Reduction on Transition Metal Nitrides

被引:14
|
作者
Yang, Xiaoju [1 ]
Xu, Bingjun [2 ]
Chen, Jingguang G. [3 ,4 ]
Yang, Xuan [1 ,3 ]
机构
[1] Huazhong Univ Sci & Technol, Key Lab Mat Chem Energy Convers & Storage, Hubei Key Lab Mat Chem & Serv Failure, Sch Chem & Chem Engn,Wuhan Natl Lab Optoelect, Wuhan 430074, Peoples R China
[2] Peking Univ, Coll Chem & Mol Engn, Beijing 100871, Peoples R China
[3] Columbia Univ, Dept Chem Engn, New York, NY 10027 USA
[4] Brookhaven Natl Lab, Chem Div, Upton, NY 11973 USA
基金
美国能源部;
关键词
ammonia; electrocatalysis; nitrides; nitrogen reduction; operando spectroscopy; VAN KREVELEN MECHANISM; AMMONIA-SYNTHESIS; ATMOSPHERIC-PRESSURE; DINITROGEN REDUCTION; AMBIENT CONDITIONS; HABER-BOSCH; CATALYSTS; N-2; PHASE; ELUCIDATION;
D O I
10.1002/cssc.202201715
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Distributed electrochemical nitrogen reduction reaction (ENRR) powered by renewable energy for the on-site production of ammonia is an attractive alternative to the industrial Haber-Bosch process, which is responsible for roughly 2 % of global energy consumption. In this Review, we summarize recent progress in the ENRR catalyzed by transition metal nitrides (TMNs). The unique electronic structures of TMNs make them promising ENRR catalysts for active and selective ammonia production, which have been predicted theoretically and demonstrated experimentally. Reaction pathways and deactivation mechanisms of the ENRR on different TMNs are surveyed, and current understanding of structure-activity relations is discussed. To develop highly active, selective, and stable TMN catalysts for industrial-scale ENRR, membrane electrode assembly configuration is recommended in catalyst evaluation. Furthermore, we highlight the importance of developing mechanistic understanding on ENRR with different operando spectroscopic techniques.
引用
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页数:12
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