Electrochemistry‐Mediated Synthesis of Hydrazine from Ammonia

L Leitao Xu (State Key Laboratory of Chemo and Biosensing, College of Chemistry and Chemical Engineering, Advanced Catalytic Engineering Research Center of the Ministry of Education) Y Yelin Yao (State Key Laboratory of Chem/Bio‐Sensing and Chemometrics College of Chemistry and Chemical Engineering Hunan University Changsha China) W Wenjie Wu W Wei Chen C Cairong Wang (State Key Laboratory of Chem/Bio‐Sensing and Chemometrics College of Chemistry and Chemical Engineering Hunan University Changsha China) Y Yandong Wu Z Zhonghuan Zhu Z Zhuoran Lu (State Key Laboratory of Chemo and Biosensing College of Chemistry and Chemical Engineering International Joint Lab of Energy Electrochemistry of the Ministry of Education Hunan University Changsha P. R. China) T Ta Thi Thuy Nga (Research Center for X-ray Science & Department of Physics) C Chung‐Li Dong (Department of Physics Tamkang University New Taipei City Taiwan) Y Yuqin Zou (State Key Laboratory of Chem/Bio-Sensing and Chemometrics, College of Chemistry and Chemical Engineering) S Shuangyin Wang (State Key Laboratory of Chem/Bio-Sensing and Chemometrics, College of Chemistry and Chemical Engineering)

Abstract

Abstract The synthesis of hydrazine from the electrooxidation of ammonia (NH 3 ) presents a promising pathway, yet it is hindered by the strong thermodynamic preference for the oxidation of hydrazine. Here, we describe an electrochemistry‐mediated strategy that reverses the thermodynamic order during NH 3 oxidation, enabling sustainable hydrazine production. This process utilizes cyclohexanone (C 6 H 10 O), derived from the electrooxidation of cyclohexanol (C 6 H 11 OH), as a mediator to prevent the over‐oxidation of NH 3 . The in situ generation of cyclohexanone (C 6 H 10 O) at the catalyst interface effectively prevents the over‐oxidation of NH 3 , while cation effect accelerates NH 3 capture during the reaction. Furthermore, the developed manganese (Mn) doped nickel hydroxide electrocatalyst (Mn‐Ni(OH) 2 ) not only improves NH 3 tolerance of the catalyst but also promotes the conversion of nitrogen‐containing intermediates. This scalable approach achieves gram‐scale production at a constant current of 800 mA, offering economic advantages over industrial methods, paving the way for a sustainable transformation of the chemical industry.

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 (12)

L

Leitao Xu

State Key Laboratory of Chemo and Biosensing, College of Chemistry and Chemical Engineering, Advanced Catalytic Engineering Research Center of the Ministry of Education

Y

Yelin Yao

State Key Laboratory of Chem/Bio‐Sensing and Chemometrics College of Chemistry and Chemical Engineering Hunan University Changsha China

W

Wenjie Wu

W

Wei Chen

C

Cairong Wang

State Key Laboratory of Chem/Bio‐Sensing and Chemometrics College of Chemistry and Chemical Engineering Hunan University Changsha China

Y

Yandong Wu

Z

Zhonghuan Zhu

Z

Zhuoran Lu

State Key Laboratory of Chemo and Biosensing College of Chemistry and Chemical Engineering International Joint Lab of Energy Electrochemistry of the Ministry of Education Hunan University Changsha P. R. China

T

Ta Thi Thuy Nga

Research Center for X-ray Science & Department of Physics

C

Chung‐Li Dong

Department of Physics Tamkang University New Taipei City Taiwan

Y

Yuqin Zou

State Key Laboratory of Chem/Bio-Sensing and Chemometrics, College of Chemistry and Chemical Engineering

S

Shuangyin Wang

State Key Laboratory of Chem/Bio-Sensing and Chemometrics, College of Chemistry and Chemical Engineering