Water‐in‐Acid Strategy for Corrosion‐Free Proton Storage: Phosphoric Acid Electrolyte Engineering Toward Sustainable Aqueous Batteries

B Baiming Su (School of Materials Science and Chemical Engineering Ningbo University Ningbo 315211 China) J Junqiang Deng (School of Materials Science and Chemical Engineering Ningbo University Ningbo 315211 China) Z Zhouxiang Wu (School of Materials Science and Chemical Engineering Ningbo University Ningbo 315211 China) X Xinran Li J Jing Li H Haoxiang Yu P Peng Li H Hui Li L Lei Yan (Department of Materials Science and Engineering) L Liyuan Zhang (State Key Laboratory of Natural Medicines and Jiangsu Key Laboratory of Drug Discovery for Metabolic Diseases, Center of Advanced Pharmaceuticals and Biomaterials) T Ting‐Feng Yi (Key Laboratory of Dielectric and Electrolyte Functional Material Hebei Province, School of Resources and Materials Northeastern University at Qinhuangdao Qinhuangdao Hebei P. R. China) T Tianyi Ma (Centre for Atomaterials and Nanomanufacturing, School of Science, Royal Melbourne Institute of Technology University) J Jie Shu

Abstract

Abstract Aqueous proton batteries, leveraging the intrinsic advantages of protons such as minimal hydrated radius, natural abundance, and rapid transport kinetics, have emerged as promising candidates for next‐generation energy storage. However, conventional strong acid electrolytes like H 2 SO 4 suffer from critical limitations including electrode dissolution and incompatibility with battery components. To circumvent these challenges, weak acids (e.g., HCOOH and H 3 PO 4 ) have been strategically selected as alternative electrolytes due to their non‐corrosive characteristics. Particularly, the implementation of high‐concentration “water‐in‐acid” (WIA) effectively suppresses undesirable interactions between electrode materials and free water molecules. Through electrolyte engineering, we developed a 9.5 M H 3 PO 4 WIA system that synergizes with a molybdenum trioxide electrode, achieving remarkable electrochemical performance: a high reversible capacity of 229.8 mAh g −1 at 3 A g −1 and exceptional cycling stability with 83.86% capacity retention after 1000 cycles at 5 A g −1 , surpassing conventional H₂SO₄‐based systems by both capacity and cyclability. This innovative approach establishes a new paradigm for developing high‐performance aqueous energy storage systems through acid‐dominated electrolyte design.

Article Details

Volume / Issue Vol. 64, Issue 25
Published June 17, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (13)

B

Baiming Su

School of Materials Science and Chemical Engineering Ningbo University Ningbo 315211 China

J

Junqiang Deng

School of Materials Science and Chemical Engineering Ningbo University Ningbo 315211 China

Z

Zhouxiang Wu

School of Materials Science and Chemical Engineering Ningbo University Ningbo 315211 China

X

Xinran Li

J

Jing Li

H

Haoxiang Yu

P

Peng Li

H

Hui Li

L

Lei Yan

Department of Materials Science and Engineering

L

Liyuan Zhang

State Key Laboratory of Natural Medicines and Jiangsu Key Laboratory of Drug Discovery for Metabolic Diseases, Center of Advanced Pharmaceuticals and Biomaterials

T

Ting‐Feng Yi

Key Laboratory of Dielectric and Electrolyte Functional Material Hebei Province, School of Resources and Materials Northeastern University at Qinhuangdao Qinhuangdao Hebei P. R. China

T

Tianyi Ma

Centre for Atomaterials and Nanomanufacturing, School of Science, Royal Melbourne Institute of Technology University

J

Jie Shu