煅烧
催化作用
法拉第效率
材料科学
电化学
钴
电解质
可逆氢电极
氨生产
电催化剂
碳纤维
氨
过渡金属
氮气
无机化学
化学工程
电极
复合数
复合材料
化学
工作电极
冶金
物理化学
有机化学
工程类
作者
Yunnan Gao,Zishan Han,Song Hong,Tianbin Wu,Xin Li,Jieshan Qiu,Zhenyu Sun
标识
DOI:10.1021/acsaem.9b01135
摘要
Electrochemical N2 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 N2 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 μgNH3 h–1 mgcat.–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 N2 activation. This work would provide an easy and alternative method for the synthesis of transition-metal catalysts for ENR.
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