Boosting the Ionic Conductivity of Non‐Aqueous Proton Electrolyte for Hybrid Capacitors

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) Y Yuxiao Lin Y Yunsong Li Y Yongjie Cao (Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, College of Smart Materials and Future Energy, Laboratory of Advanced Materials) G Guodong Li (Chinese Academy of Sciences (CAS) Key Laboratory of Nanosystem and Hierarchical Fabrication, CAS Center for Excellence in Nanoscience) D Dewei Xiao (Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, College of Smart Materials and Future Energy, Laboratory of Advanced Materials) Z Ziyue Li Y Yi Yang F Fei Wang Y Yongyao Xia

Abstract

Abstract Proton batteries have emerged as promising alternatives for energy storage owing to their rapid H⁺ transport kinetics and environmental sustainability. However, state‐of‐art proton batteries using aqueous acid electrolytes suffer from severe hydrogen evolution, electrode dissolution, and narrow electrochemical windows. Non‐aqueous electrolytes could obviate these challenges, while they are typically limited by low ionic conductivity. In this work, a hydrogen‐bond‐mediated proton transport mechanism is revealed in the phosphoric acid/ethyl acetate (H 3 PO 4 /EA) electrolytes with various concentrations. The optimized non‐aqueous H 3 PO 4 /EA electrolyte (80 m) simultaneously achieves high ionic conductivity (21.8 mS cm −1 ), wide electrochemical stability window (2.5 V), wide operational temperature range (−80 to 200 °C), and minimal corrosiveness. Using this electrolyte, the MoO 3 //AC hybrid capacitor demonstrates ultrahigh power density (13292 W kg −1 ), extended cycling stability (10 000 cycles), and unprecedented temperature adaptability (−50 to 60   °C). Our findings provide fundamental insights into non‐aqueous proton conduction mechanisms and establish new design principles for practical proton energy storage systems.

Article Details

Volume / Issue Vol. 64, Issue 47
Published November 17, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

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

Y

Yuxiao Lin

Y

Yunsong Li

Y

Yongjie Cao

Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, College of Smart Materials and Future Energy, Laboratory of Advanced Materials

G

Guodong Li

Chinese Academy of Sciences (CAS) Key Laboratory of Nanosystem and Hierarchical Fabrication, CAS Center for Excellence in Nanoscience

D

Dewei Xiao

Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, College of Smart Materials and Future Energy, Laboratory of Advanced Materials

Z

Ziyue Li

Y

Yi Yang

F

Fei Wang

Y

Yongyao Xia