{"title":"Boosting the Ionic Conductivity of Non‐Aqueous Proton Electrolyte for Hybrid Capacitors","authors":"Mochou Liao, Yuxiao Lin, Yunsong Li, Yongjie Cao, Guodong Li, Dewei Xiao, Ziyue Li, Yi Yang, Fei Wang, Yongyao Xia","doi":"10.1002/anie.202516992","DOIUrl":null,"url":null,"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<jats:sub>3</jats:sub>PO<jats:sub>4</jats:sub>/EA) electrolytes with various concentrations. The optimized non‐aqueous H<jats:sub>3</jats:sub>PO<jats:sub>4</jats:sub>/EA electrolyte (80 m) simultaneously achieves high ionic conductivity (21.8 mS cm<jats:sup>−1</jats:sup>), wide electrochemical stability window (2.5 V), wide operational temperature range (−80 to 200 °C), and minimal corrosiveness. Using this electrolyte, the MoO<jats:sub>3</jats:sub>//AC hybrid capacitor demonstrates ultrahigh power density (13292 W kg<jats:sup>−1</jats:sup>), extended cycling stability (10 000 cycles), and unprecedented temperature adaptability (−50 to 60<jats:sup> </jats:sup>°C). Our findings provide fundamental insights into non‐aqueous proton conduction mechanisms and establish new design principles for practical proton energy storage systems.","PeriodicalId":125,"journal":{"name":"Angewandte Chemie International Edition","volume":"100 1","pages":""},"PeriodicalIF":16.9000,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie International Edition","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/anie.202516992","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
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 (H3PO4/EA) electrolytes with various concentrations. The optimized non‐aqueous H3PO4/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 MoO3//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.
质子电池由于其快速的H +传输动力学和环境可持续性,已经成为储能的有希望的替代品。然而,使用酸性水溶液的质子电池存在严重的析氢、电极溶解和狭窄的电化学窗口等问题。非水电解质可以避免这些挑战,但它们通常受到低离子电导率的限制。在这项工作中,揭示了在不同浓度的磷酸/乙酸乙酯(H3PO4/EA)电解质中氢键介导的质子传输机制。优化的非水相H3PO4/EA电解质(80 m)同时具有高离子电导率(21.8 mS cm−1),宽电化学稳定窗口(2.5 V),宽工作温度范围(- 80至200°C)和最小的腐蚀性。使用这种电解质,MoO3//交流混合电容器具有超高功率密度(13292 W kg−1),延长循环稳定性(10,000次循环)和前所未有的温度适应性(−50至60°C)。我们的发现为非水质子传导机制提供了基本的见解,并为实用的质子储能系统建立了新的设计原则。
期刊介绍:
Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.