Acid‐Alkaline Double Electrolytes for High‐Energy Aqueous Proton Batteries

Z Ziyue Li F Fengmei Wang (State Key Laboratory of Chemical Resource Engineering, College of Chemistry) J Jinyu Yang X Xinjie Li M Mingxu Wang P Pengfei Zhang M Mochou Liao (Department of Chemistry Department of Materials Science College of Smart Materials and Future Energy Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials Fudan University Shanghai 200433 China) J Jiafeng Ruan S Sainan Luo (School of Materials and Chemistry University of Shanghai for Science and Technology Shanghai 200093 China) J Junjie Chi (College of Smart Materials and Future Energy Fudan University Shanghai 200433 China) X Xuelian Qu R Ruohan Jiang (College of Smart Materials and Future Energy Fudan University Shanghai 200433 China) Z Zihao Zhang (Shanghai Engineering Research Center of Tooth Restoration and Regeneration and Tongji Research Institute of Stomatology and Department of Implantology, Shanghai Tongji Stomatological Hospital and Dental School, Tongji University) C Chaoxin Wu (College of Smart Materials and Future Energy Fudan University Shanghai 200433 P.R. China) D Dalin Sun F Fang Fang F Fei Wang

Abstract

Abstract Aqueous proton batteries offer a promising energy storage solution due to their inherent safety, rapid ion mobility, and low cost. However, their performance is largely constrained by water's limited electrochemical stability, restricting operating voltage and energy density. This study addresses this challenge by introducing an innovative acid‐alkaline double electrolyte configuration to achieve high‐voltage aqueous proton batteries. Employing a high‐anodic‐limit acidic catholyte (7 M H 3 PO 4 ) and a low‐cathodic‐limit alkaline anolyte (6 M KOH), separated by a proton exchange membrane (PEM), significantly expands the full battery's electrochemical stability window (ESW) to 2.91 V. Cobalt‐doped Prussian blue (CoCuHCF) was selected as the cathode due to its superior proton kinetics and cycling durability, while benzo[c]cinnoline (BCC) was identified as an optimal anode via combined theoretical analysis and experimental validation. Consequently, the battery delivered exceptional electrochemical performance, achieving a high energy density of 329.6 Wh kg −1 at 1 A g −1 , a remarkable power density of 14788.3 W kg −1 at 10 A g −1 , and excellent cycling stability with 98.3% capacity retention after 1000 cycles. The proposed acid‐alkaline double electrolyte strategy provides efficient and valuable guidance for advancing aqueous energy storage technologies.

Article Details

Volume / Issue Vol. 64, Issue 42
Published October 13, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (17)

Z

Ziyue Li

F

Fengmei Wang

State Key Laboratory of Chemical Resource Engineering, College of Chemistry

J

Jinyu Yang

X

Xinjie Li

M

Mingxu Wang

P

Pengfei Zhang

M

Mochou Liao

Department of Chemistry Department of Materials Science College of Smart Materials and Future Energy Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials Fudan University Shanghai 200433 China

J

Jiafeng Ruan

S

Sainan Luo

School of Materials and Chemistry University of Shanghai for Science and Technology Shanghai 200093 China

J

Junjie Chi

College of Smart Materials and Future Energy Fudan University Shanghai 200433 China

X

Xuelian Qu

R

Ruohan Jiang

College of Smart Materials and Future Energy Fudan University Shanghai 200433 China

Z

Zihao Zhang

Shanghai Engineering Research Center of Tooth Restoration and Regeneration and Tongji Research Institute of Stomatology and Department of Implantology, Shanghai Tongji Stomatological Hospital and Dental School, Tongji University

C

Chaoxin Wu

College of Smart Materials and Future Energy Fudan University Shanghai 200433 P.R. China

D

Dalin Sun

F

Fang Fang

F

Fei Wang