High‐Yield Ammonia Production from Al‐Nitrate Battery via Anodic Al&amp;NO <sub>3</sub> <sup>−</sup> Spontaneous Reaction Driven Cathodic Nitrate Reduction Reaction

L Li‐Li Chen (School of Interdisciplinary Science Beijing Institute of Technology Beijing P. R. China) W Wanqiang Yu (Institute for Advanced Interdisciplinary Research (iAIR) School of Chemistry and Chemical Engineering University of Jinan Jinan 250022 P. R. China) Y Yijie Wang Y Yuke Chen M Man Huang (Key Laboratory of Multiple Organ Failure (Ministry of Education), Departments of Microbiology and General Intensive Care Unit of the Second Affiliated Hospital, Zhejiang University School of Medicine) H Hua Tan (College of Future Information Technology) X Xin Liu K Kai Jiang (Department of Pharmacy, The First Affiliated Hospital of the University of Science and Technology of China, and State Key Laboratory of Precision and Intelligent Chemistry) S Shuqiang Jiao H Hong Liu W Weijia Zhou

Abstract

Abstract The electrocatalytic nitrate reduction reaction (NIRR) offers a sustainable alternative for ammonia (NH 3 ) synthesis, addressing the limitations of the energy‐intensive Haber‐Bosch process. This study introduces a novel aluminum‐nitrate (Al‐NO 3 − ) battery system that integrates anodic Al and NO 3 − (Al&amp;NO 3 − ) spontaneous reactions with cathodic NO 3 − reduction, enabling simultaneous NH 3 production and electricity generation. The CuNi alloy films, synthesized via pulse laser confined bombardment (PLCB) technology, serve as efficient NIRR cathodes with tandem catalytic sites, delivering an NH 3 production rate of ≈58.04 mg h −1 cm −2 with a Faradaic efficiency (FE) of 99.40% at −1.3 V vs. Hg/HgO. The Al‐NO 3 − battery system, incorporating NO 3 − in both anodic and cathodic electrolytes, suppresses hydrogen evolution at the anode, and achieves an apparent FE exceeding 100% due to NO 3 − consumption for NH 3 production through both cathodic NIRR and the spontaneous anodic Al&amp;NO 3 − reaction. Extended stability studies indicated continuous operation exceeding 50 h, with peak apparent FE reaching ≈183.60%. This system demonstrates a high NH 3 yield of over 10.0 mg h −1 cm −2 at a current density of 40 mA cm −2 . The findings highlight the potential of Al&amp;NO 3 − spontaneous reactions to drive cathodic NO 3 − reduction, offering a sustainable pathway for NH 3 synthesis from NO 3 − ‐rich wastewater while generating electrical energy.

Article Details

Volume / Issue Vol. 38, Issue 9
Published February 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (11)

L

Li‐Li Chen

School of Interdisciplinary Science Beijing Institute of Technology Beijing P. R. China

W

Wanqiang Yu

Institute for Advanced Interdisciplinary Research (iAIR) School of Chemistry and Chemical Engineering University of Jinan Jinan 250022 P. R. China

Y

Yijie Wang

Y

Yuke Chen

M

Man Huang

Key Laboratory of Multiple Organ Failure (Ministry of Education), Departments of Microbiology and General Intensive Care Unit of the Second Affiliated Hospital, Zhejiang University School of Medicine

H

Hua Tan

College of Future Information Technology

X

Xin Liu

K

Kai Jiang

Department of Pharmacy, The First Affiliated Hospital of the University of Science and Technology of China, and State Key Laboratory of Precision and Intelligent Chemistry

S

Shuqiang Jiao

H

Hong Liu

W

Weijia Zhou