Interfacial Water Structure Modulation on Unconventional Phase Non-Precious Metal Alloy Nanostructures for Efficient Nitrate Electroreduction to Ammonia in Neutral Media

Yunhao Wang (Co-first Author), Fengkun Hao (Co-first Author), Hongming Xu (Co-first Author), Mingzi Sun (Co-first Author), Xixi Wang, Yuecheng Xiong, Jingwen Zhou, Fu Liu, Yubing Hu, Yangbo Ma, Xiang Meng, Liang Guo, Chaohui Wang, Mingzheng Shao, Guozhi Wang, Juan Wang, Pengyi Lu, Jinwen Yin, Jie Wang, Wenxin NiuChenliang Ye, Qinghua Zhang, Shibo Xi, Bolong Huang*, Minhua Shao*, Zhanxi Fan*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

2 Citations (Scopus)

Abstract

Electrocatalytic nitrate reduction reaction (NO3RR) has been recognized as a sustainable route for nitrate removal and value-added ammonia (NH3) synthesis. Regulating the surface active hydrogen (*H) behavior is crucial but remains a formidable challenge, especially in neutral electrolytes, greatly limiting the highly selective NH3 formation. Herein, we report the controlled synthesis of heterophase hcp/fcc non-precious CuNi alloy nanostructures for efficient NH3 electrosynthesis in neutral media. Significantly, hcp/fcc Cu10Ni90 exhibits excellent performance with NH3 Faradaic efficiency and yield rate of 98.1% and 57.4 mg h-1 mgcat-1, respectively. In situ studies suggest that the high proportion of interfacial K+ ion hydrated water (K+-H2O) on hcp/fcc Cu10Ni90 creates high *H coverage via boosting interfacial water dissociation, enabling the rapid hydrogenation kinetics for NH3 synthesis. Theoretical calculations reveal that the superior NO3RR performance of hcp/fcc Cu10Ni90 originates from both the existence of hcp phase to improve the electroactivity and the high Ni content to guarantee an efficient active hydrogen supply. The strong interaction between Ni and Cu also optimizes the electronic structures of Cu sites to realize fast intermediate conversions with low energy barriers. This work provides a novel strategy to optimize surface *H behavior via tuning interfacial water structure by crystal phase control. © 2025 Wiley-VCH GmbH.
Original languageEnglish
Article numbere202508617
Journal Angewandte Chemie International Edition
Volume64
Issue number28
Online published5 May 2025
DOIs
Publication statusPublished - Jul 2025

Funding

This work was supported by grants (Project Nos. 22175148,52250402, and 52025025) from National Natural Science Foundation of China, grants (Project Nos. 21309322, 15304023,15304724, N_PolyU502/21, CRS_PolyU504/22 and C1003-23Y)from Research Grants Council of Hong Kong, grant (Project Nos.JCYJ20220530140815035 and JCYJ20220531090807017) from Shenzhen Science and Technology Program, ITC via Hong Kong Branch of National Precious Metals Material Engineering Research Centre (NPMM), and grants (Project Nos. 9610480,9610663, 7006007, 7020103, and 9680301) from City University of Hong Kong. M.S. acknowledges the financial support by Guangzhou Science and Technology Bureau (Project No.2024A03J0609). Ji. W. thanks the financial support from the Key Project of Sichuan Province (Project No. 2025YFHZ0225) and Chengdu Vehicle Environmental Protection Technology Co., Ltd(Project No. 2023-CDVEPTKF-04).

Research Keywords

  • Ammonia electrosynthesis
  • Electrocatalysis
  • Interfacial water structure
  • Non-precious metal nanoalloys
  • Phase control

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