ZIF-67-Derived Cobalt/Nitrogen-Doped Carbon Composites for Efficient Electrocatalytic N2 Reduction

被引:85
作者
Gao, Yunnan [1 ]
Han, Zishan [1 ]
Hong, Song [2 ]
Wu, Tianbin [3 ]
Li, Xin [1 ]
Qiu, Jieshan [1 ]
Sun, Zhenyu [1 ,4 ]
机构
[1] Beijing Univ Chem Technol, Coll Chem Engn, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
[2] Beijing Univ Chem Technol, Coll Mat Sci & Engn, Beijing 100029, Peoples R China
[3] Chinese Acad Sci, Inst Chem, Key Lab Colloid & Interface & Thermodynam, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
[4] Beijing Univ Chem Technol, Beijing Key Lab Energy Environm Catalysis, Beijing 100029, Peoples R China
基金
北京市自然科学基金;
关键词
N-2; reduction; electrocatalysis; cobalt; nitrogen-doped carbon; metal-organic frameworks; METAL-ORGANIC FRAMEWORK; OXYGEN REDUCTION; HYDROGEN EVOLUTION; AMBIENT CONDITIONS; NITROGEN-FIXATION; AMMONIA-SYNTHESIS; ACTIVE-SITES; ELECTROSYNTHESIS; GRAPHENE;
D O I
10.1021/acsaem.9b01135
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
Electrochemical N-2 reduction (ENR) provides a potential approach for NH3 synthesis. To facilitate ENR, the development of naturally abundant, cheap, and effective electrocatalysts is critically important. Herein, we report Co/nitrogen-doped carbon composites comprising a large number of single Co sites for efficient N-2 electrofixation at ambient conditions. The N configurations and Co species in the catalysts are readily tunable by controlling the calcination temperatures. Such low-cost catalysts enhanced electrochemical reduction of dinitrogen to ammonia, yielding a maximum ammonia production rate of about 5.1 mu g(NH3) h(-1) mg(cat).(-1) at -0.4 V (vs. the reversible hydrogen electrode, RHE) and a Faradaic efficiency of up to 10.1% at -0.1 V (vs. RHE) in 0.1 M KOH electrolyte. We inferred that single Co atoms together with pyrrolic N may be major active sites for N-2 activation. This work would provide an easy and alternative method for the synthesis of transition-metal catalysts for ENR.
引用
收藏
页码:6071 / 6077
页数:13
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