纳米花
电催化剂
纳米线
材料科学
硝酸盐
纳米技术
化学工程
还原(数学)
化学
纳米结构
电极
电化学
物理化学
几何学
工程类
有机化学
数学
作者
Jingwen Yu,Yunliang Liu,Cunhao Fan,Naiyun Liu,Jingya Yin,Yaxi Li,Yuanyuan Cheng,Xinya Yuan,Xinyue Zhang,Yixian Liu,Sanjun Fan,Lei Xu,Haitao Li
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2024-12-16
卷期号:18 (2): 94907135-94907135
被引量:28
标识
DOI:10.26599/nr.2025.94907135
摘要
Electrocatalytic nitrate reduction reaction (NitRR) is an efficient route for simultaneous wastewater treatment and ammonia production, but the conversion of NO3– to NH3 involves multiple electron and proton transfer processes and diverse by-products. Therefore, developing ammonia catalysts with superior catalytic activity and selectivity is an urgent task. The distinctive electronic structure of Cu enhances the adsorption of nitrogen-containing intermediates, but the insufficient activation capability of Cu for interfacial water restricts the generation of reactive hydrogen and inhibits the hydrogenation process. In this work, a Ce-doped CuO catalyst (Ce10/CuO) was synthesized by in situ oxidative etching and annealing. The redox of Ce3+/Ce4+ enables the optimization of the electronic structure of the catalyst, and the presence of Ce3+ as a defect indicator introduces more oxygen vacancies. The results demonstrate that Ce10/CuO provides an impressive ammonia yield of 3.88 ± 0.14 mmol·cm–2·h–1 at 0.4 V vs. reversible hydrogen electrode (RHE) with an increase of 1.04 mmol·cm–2·h–1 compared to that of pure CuO, and the Faradaic efficiencies (FE) reaches 93.2% ± 3.4%. In situ characterization confirms the doping of Ce facilitates the activation and dissociation of interfacial water, which promotes the production of active hydrogen and thus enhances the ammonia production efficiency.
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