Co <sub>1</sub> Zn Single‐Atom Alloy Boosts Active Hydrogen Spillover for Highly Efficient Electrosynthesis of Ammonia Over 2 A cm <sup>−2</sup> Current Density

Z Zhipeng Chen (School of Chemistry and Chemical Engineering) G Gen Liu (Key Laboratory of Catalysis and Energy Materials Chemistry of Ministry of Education & Hubei Key Laboratory of Catalysis and Materials Science) Y Yusi Zhao (School of Chemistry and Chemical Engineering) Y Yan Yan Q Qingping Ke (School of Chemistry and Chemical Engineering Anhui Province Key Laboratory of Coal Clean Conversion and Low Carbon Utilization Anhui University of Technology Ma'anshan 243032 P.R. China) C Chao Wan Z Zhirong Zhang (Hefei National Research Center for Physical Sciences at the Microscale, Key Laboratory of Strongly-Coupled Quantum Matter Physics of Chinese Academy of Sciences, Key Laboratory of Surface and Interface Chemistry and Energy Catalysis of Anhui Higher Education Institutes, Department of Chemical Physics) J Jiaxin Yuan (State Key Laboratory of Power Grid Environmental Protection) H Hongliang Li (Hefei National Research Center for Physical Sciences at the Microscale) M Mingkai Liu (School of Chemistry & Chemical Engineering) J Jie Zeng (School of Chemistry & Chemical Engineering)

Abstract

Abstract Electroreduction of nitrate to ammonia reaction (NO 3 RR) involves a series of hydrogenation steps involving nitrate‐derived intermediates. Consequently, accelerating the provision of active hydrogen is expected to enhance the reaction kinetics. In this work, we report a Co 1 Zn single‐atom alloy (SAA) catalyst that exhibits a pronounced hydrogen spillover effect. By virtue of this spillover phenomenon, the Co 1 Zn SAA nanosheets (Co 1 Zn NSs) achieve nitrate electroreduction at ampere‐level current densities. Specifically, Co 1 Zn NSs deliver a high current density of 2.4 A cm −2 (corresponding to an ammonia yield rate of 204.5 mg h −1 cm −2 ) with a Faradaic efficiency of 98.7% for ammonia production, which is approximately 2.5‐fold higher than that obtained with Zn nanosheets lacking hydrogen spillover effect. Moreover, Co 1 Zn NSs demonstrate a great application potential in Zn−NO 3 − rechargeable battery. In situ electrochemical impedance spectroscopy (EIS), in situ electron paramagnetic resonance spectroscopy (EPR), and density functional theory (DFT) calculations reveal that the isolated Co atoms in Co 1 Zn NSs served as a “hydrogen pump” for hydrogen spillover during NO 3 RR, thereby increasing the coverage of active hydrogen on the catalyst surface and lowering the energy barrier of the rate‐determining step of NO 3 RR, and finally markedly enhanced the catalytic performance.

Article Details

Volume / Issue Vol. 65, Issue 4
Published January 22, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (11)

Z

Zhipeng Chen

School of Chemistry and Chemical Engineering

G

Gen Liu

Key Laboratory of Catalysis and Energy Materials Chemistry of Ministry of Education & Hubei Key Laboratory of Catalysis and Materials Science

Y

Yusi Zhao

School of Chemistry and Chemical Engineering

Y

Yan Yan

Q

Qingping Ke

School of Chemistry and Chemical Engineering Anhui Province Key Laboratory of Coal Clean Conversion and Low Carbon Utilization Anhui University of Technology Ma'anshan 243032 P.R. China

C

Chao Wan

Z

Zhirong Zhang

Hefei National Research Center for Physical Sciences at the Microscale, Key Laboratory of Strongly-Coupled Quantum Matter Physics of Chinese Academy of Sciences, Key Laboratory of Surface and Interface Chemistry and Energy Catalysis of Anhui Higher Education Institutes, Department of Chemical Physics

J

Jiaxin Yuan

State Key Laboratory of Power Grid Environmental Protection

H

Hongliang Li

Hefei National Research Center for Physical Sciences at the Microscale

M

Mingkai Liu

School of Chemistry & Chemical Engineering

J

Jie Zeng

School of Chemistry & Chemical Engineering