化学
纳米片
电化学
法拉第效率
电解质
产量(工程)
硫黄
密度泛函理论
可逆氢电极
催化作用
无机化学
电极
物理化学
计算化学
有机化学
冶金
材料科学
工作电极
作者
Longcheng Zhang,Qiang Zhou,Jie Liang,Luchao Yue,Tingshuai Li,Yongsong Luo,Qian Liu,Na Li,Bo Tang,Feng Gong,Xiaodong Guo,Xuping Sun
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2022-05-10
卷期号:61 (20): 8096-8102
被引量:58
标识
DOI:10.1021/acs.inorgchem.2c01112
摘要
Electrochemical reduction of NO to NH3 is of great significance for mitigating the accumulation of nitrogen oxides and producing valuable NH3. Here, we demonstrate that the CoS nanosheet with sulfur vacancies (CoS1-x) behaves as an efficient catalyst toward electrochemical NO-to-NH3 conversion. In 0.2 M Na2SO4 electrolyte, such CoS1-x displays a large NH3 yield rate (44.67 μmol cm-2 h-1) and a high Faradaic efficiency (53.62%) at -0.4 V versus the reversible hydrogen electrode, outperforming the CoS counterpart (27.02 μmol cm-2 h-1; 36.68%). Moreover, the Zn-NO battery with CoS1-x shows excellent performance with a power density of 2.06 mW cm-2 and a large NH3 yield rate of 1492.41 μg h-1 mgcat.-1. Density functional theory was performed to obtain mechanistic insights into the NO reduction over CoS1-x.
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