Ambient ammonia production via electrocatalytic nitrate reduction catalyzed by a flower-like CuCo2O4 electrocatalyst

被引:22
|
作者
Wang, Jinlu [1 ,2 ]
Zhang, Shengbo [2 ]
Wang, Chenchen [3 ]
Li, Ke [2 ]
Zha, Yuankang [2 ]
Liu, Min [2 ]
Zhang, Haimin [2 ]
Shi, Tongfei [2 ]
机构
[1] Anhui Univ, Inst Phys Sci, Hefei 230601, Peoples R China
[2] Chinese Acad Sci, Inst Solid State Phys, Key Lab Mat Phys, HFIPS, Hefei 230031, Peoples R China
[3] Shanghai Nucl Engn Res & Design Inst Co Ltd, Shanghai 200233, Peoples R China
来源
INORGANIC CHEMISTRY FRONTIERS | 2022年 / 9卷 / 10期
基金
中国博士后科学基金;
关键词
D O I
10.1039/d1qi01656c
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The electrochemical nitrate reduction reaction (NtRR) under ambient conditions is regarded as a potential approach to achieve NH3 production, which currently heavily relies on the Haber-Bosch process at the cost of a huge amount of energy and the massive production of CO2. Herein, a flower-like CuCo2O4 spinel was synthesized via a two-step urea-assisted hydrothermal treatment and calcination process. When used as the electrocatalyst for the NtRR, the as-synthesized CuCo2O4 spinel exhibits a high electrocatalytic activity, affording a high NH3 yield rate of 48.8 mu g h(-1) cm(-2) at -0.85 V (vs. RHE) and a high faradaic efficiency (FE) of 34.2% at -0.45 V (vs. RHE). The N-15 isotopic labelling experiments confirm that the yielded NH3 is, indeed, from the CuCo2O4 spinel catalyzed NtRR process. Our theoretical calculations results reveal that the NO3- can be adsorbed on the CuCo2O4 to form the *NOH intermediate, leading to a good selectivity and FE.
引用
收藏
页码:2374 / 2378
页数:5
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