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Research Article | Open Access

A nanoflower-on-nanowire heterogeneous electrocatalyst for enhanced interfacial water activation in nitrate reduction reaction

Jingwen Yu1Yunliang Liu1Cunhao Fan1Naiyun Liu1 ( )Jingya Yin2Yaxi Li1Yuanyuan Cheng1Xinya Yuan1Xinyue Zhang1Yixian Liu1Sanjun Fan3( )Lei Xu4,5( )Haitao Li1 ( )
Institute for Energy Research, School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013, China
Qingdao Municipal Center for Disease Control and Prevention, Qingdao 266033, China
Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio 43210, USA
Jiangsu Engineering Technology Research Center of Biomass Composites and Addictive Manufacturing, Institute of Agricultural Facilities and Equipment, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China
Key Laboratory for Protected Agricultural Engineering in the Middle and Lower Reaches of Yangtze River, Ministry of Agriculture and Rural Affairs, Nanjing 210014, China
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Abstract

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.

Graphical Abstract

A nanoflower-on-nanowire cerium-doped copper oxide heterogeneous electrocatalyst was prepared through in situ etching and ion exchange for the electrocatalytic reduction of nitrate to ammonia. Cerium doping can effectively promote the activation of the catalyst for interfacial water by introducing vacancies and optimizing the electronic structure, thus enhancing the generation of active hydrogen and the reduction of nitrate to ammonia.

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Nano Research
Article number: 94907135

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Cite this article:
Yu J, Liu Y, Fan C, et al. A nanoflower-on-nanowire heterogeneous electrocatalyst for enhanced interfacial water activation in nitrate reduction reaction. Nano Research, 2025, 18(2): 94907135. https://doi.org/10.26599/NR.2025.94907135
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Received: 23 October 2024
Revised: 09 November 2024
Accepted: 12 November 2024
Published: 07 January 2025
© The Author(s) 2025. Published by Tsinghua University Press.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).