可逆氢电极
电催化剂
材料科学
氨
法拉第效率
产量(工程)
催化作用
电化学
氧化物
碳纤维
纳米晶
化学工程
无机化学
氢
氨生产
纳米技术
电极
化学
物理化学
有机化学
工作电极
复合数
工程类
复合材料
冶金
作者
Ge Meng,Mengmeng Jin,Tianran Wei,Qian Liu,Shusheng Zhang,Xianyun Peng,Jun Luo,Xijun Liu
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2022-08-18
卷期号:15 (10): 8890-8896
被引量:76
标识
DOI:10.1007/s12274-022-4747-y
摘要
Electrochemical nitric oxide reduction reaction (NORR) to produce ammonia (NH3) under ambient conditions is a promising alternative to the energy and carbon-intensive Haber-Bosch approach, but its performance is still improved. Herein, molybdenum carbides (MoC) nanocrystals confined by nitrogen-doped carbon nanosheets are first designed as an efficient and durable electrocatalyst for catalyzing the reduction of NO to NH3 with maximal Faradaic efficiency of 89% ± 2% and a yield rate of 1,350 ± 15 µg·h−1·cm−2 at the applied potential of −0.8 V vs. reversible hydrogen electrode (RHE) as well as high stable activity with negligible current density and NH3 yield rate decays over a 30 h continue the test. Moreover, as a proof-of-concept of Zn−NO battery, it achieves a peak power density of 1.8 mW·cm−2 and a large NH3 yield rate of 782 ± 10 µg·h−1·cm−2, which are comparable to the best-reported results. Theoretical calculations reveal that the MoC(111) has a strong electronic interaction with NO molecules and thus lowering the energy barrier of the potential-determining step and suppressing hydrogen evolution kinetics. This work suggests that Mo-based materials are a powerful platform providing great opportunities to explore highly selective and active catalysts for NH3 production.
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