电解质
离子电导率
电化学窗口
电导率
电化学
磷酸
材料科学
质子
超级电容器
质子输运
电容器
离子键合
化学工程
储能
热传导
无机化学
化学
快离子导体
导电体
化学物理
电极
功率密度
质子导体
纳米技术
电化学电位
氢
活化能
离子
作者
Mochou Liao,Yuxiao Lin,Yunsong Li,Yongjie Cao,Guodong Li,Dewei Xiao,Z. J. Li,Yi Yang,Fei Wang,Yongyao Xia
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-09-30
卷期号:64 (47): e202516992-e202516992
被引量:1
标识
DOI:10.1002/anie.202516992
摘要
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.
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