电催化剂
纳米孔
氨
催化作用
硝酸盐
无机化学
氨生产
化学
重组
电化学
化学工程
材料科学
纳米技术
电极
业务
物理化学
有机化学
工程类
财务
作者
Xue Zhou,Wence Xu,Yanqin Liang,Hui Jiang,Zhaoyang Li,Shuilin Wu,Zhonghui Gao,Zhenduo Cui,Shengli Zhu
标识
DOI:10.1021/acscatal.4c03336
摘要
The electrochemical nitrate (NO3–) reduction reaction (NITRR) to ammonia (NH3) offers an environmentally friendly alternative for NH3 synthesis but suffers from limited NH3 yield and low Faradaic efficiency (FE) due to the sluggish kinetics of the hydrogenation process. Herein, nanoporous Cu/CoOOH heterostructure is reported as an efficient electrocatalyst for NITRR. The catalyst achieves a high NH3 yield rate of 275.9 μmol h–1 cm–2 (689.8 mmol h–1 gcat–1) and 836.8 μmol h–1 cm–2 (2092.0 mmol h–1 gcat–1), with corresponding FE values of 85.3 and 91.5% in 200 and 1400 ppm of NO3–-N electrolyte, respectively. In situ Raman spectra reveal that the Cu/CoOOH heterostructure is derived from synergistic chemical/electrochemical redox reaction between NO3– and the CuCo alloy during the NITRR process. Theoretical simulations indicate that Cu/CoOOH exhibits enhanced *NO2 affinity and reduces the energy barrier in the rate-determining *NO2H formation step, effectively facilitating NO3– reduction to NH3.
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