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Research Article | Open Access

N-bridge anchored asymmetric AgCu dual-atomic catalysts on MXene for efficient nitrate reduction

Huilong Geng1,§Zhiyi Sun1,§Chen Li2,§Liping Wang1Ziteng Zhang1Yinqi Li1Ziheng Zhan1Yan Gao3 ( )Zhuo Chen1Zihao Wei1 ( )Shenghua Li1 ( )
School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100081, China
Beijing Key Laboratory of Microstructure and Property of Solids, Faculty of Materials and Manufacturing, Beijing University of Technology, Beijing 100124, China
Anhui Provincial Engineering Research Center of Silicon-based Materials, Bengbu University, Bengbu 233030, China

§ Huilong Geng, Zhiyi Sun, and Chen Li contributed equally to this work.

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Abstract

Electrocatalytic nitrate reduction reaction (NO3RR) offers a promising route for sustainable ammonia synthesis and wastewater treatment, yet designing highly active and selective catalysts remains challenging. Herein, we construct an N-bridge anchored asymmetric AgCu dual-atomic catalyst (DAC) on Ti3C2Tx MXene (AgCu DAC/Ti3C2Tx) for efficient nitrate electroreduction. The unique N-bridged structure stabilizes the asymmetric AgCu dual sites, enabling synergistic adsorption and activation of nitrate intermediates. In situ X-ray absorption fine structure (XAFS) spectroscopy confirms the dynamic evolution of the Ag–Cu coordination under reaction conditions, revealing their maintained heteronuclear pairing and electronic coupling during NO3RR. As a result, the AgCu DAC/Ti3C2Tx catalyst achieves a high NH3 Faradaic efficiency of ~ 97.1% with an exceptional yield rate of ~ 3.1 mg·h−1·cm−2 at −0.5 V vs. reversible hydrogen electrode (RHE), surpassing most reported dual-atom catalysts. This work provides insights into the design of asymmetric dual-atomic sites for multi-step catalytic reactions.

Graphical Abstract

An N-bridged asymmetric AgCu dual-atomic catalyst is engineered on MXene, where Ag and Cu sites work synergistically to drive efficient nitrate-to-ammonia electroreduction. In situ X-ray absorption fine structure (XAFS) captures the dynamic stabilization of Ag–Cu heteronuclear pairs under operation, while kinetic studies reveal their tandem roles: Ag enhances nitrate adsorption and Cu accelerates hydrogenation. The catalyst achieves ~ 97.1% NH3 Faradaic efficiency, offering a design blueprint for asymmetric dual-site catalysis.

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Nano Research
Article number: 94908127

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Cite this article:
Geng H, Sun Z, Li C, et al. N-bridge anchored asymmetric AgCu dual-atomic catalysts on MXene for efficient nitrate reduction. Nano Research, 2026, 19(5): 94908127. https://doi.org/10.26599/NR.2025.94908127
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Received: 30 June 2025
Revised: 22 September 2025
Accepted: 30 September 2025
Published: 20 April 2026
© The Author(s) 2026. 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/).