{"title":"Highly Proton-Conductive Solid-State Electrolyte Based on Covalent Organic Framework for Proton Battery Application.","authors":"Bing Tang, Sheng-Ting Liu, Xin-Rui Ma, Feng-Jia Zhao, Guo-Qin Zhang, Xu-Sheng Gao, Jiazhi Yang, Hong-Bin Luo, Xiao-Ming Ren","doi":"10.1021/acsami.5c09195","DOIUrl":null,"url":null,"abstract":"<p><p>Solid-state proton batteries are emerging as promising technologies for energy storage. However, efficient solid-state protonic electrolyte development remains in its early stages. Herein, we report the preparation and potential application of a high-performance covalent organic framework (COF)-based protonic electrolyte for solid-state proton batteries. Using a mechanochemical method, H<sub>3</sub>PO<sub>4</sub> was incorporated into the channels of a sulfonated COF (COF-SO<sub>3</sub>H) to produce the composite solid-state electrolyte, H<sub>3</sub>PO<sub>4</sub>@COF-SO<sub>3</sub>H. This composite was thoroughly characterized using techniques such as powder X-ray diffraction, <sup>13</sup>C NMR spectroscopy, X-ray photoelectron spectroscopy, and nitrogen adsorption/desorption analysis. Impedance spectroscopy revealed that H<sub>3</sub>PO<sub>4</sub>@COF-SO<sub>3</sub>H exhibited superprotonic conductivity exceeding 10<sup>-2</sup> S cm<sup>-1</sup> under ambient conditions, alongside remarkable long-term stability and a broad electrochemical stability window. A solid-state proton battery assembled using H<sub>3</sub>PO<sub>4</sub>@COF-SO<sub>3</sub>H as the electrolyte demonstrated exceptional performance, including excellent rate capability, high specific capacity of 101.8 mAh g<sup>-1</sup> at 1.0 A g<sup>-1</sup>, and good cycling stability with a capacity retention of 80.6% after 1000 cycles at 1.0 A g<sup>-1</sup>, outperforming previously reported solid-state proton batteries. These findings suggest that COF-based composite solid-state electrolytes hold significant promise for future applications in solid-state proton batteries.</p>","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":" ","pages":"42004-42010"},"PeriodicalIF":8.3000,"publicationDate":"2025-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Materials & Interfaces","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acsami.5c09195","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/7/10 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Solid-state proton batteries are emerging as promising technologies for energy storage. However, efficient solid-state protonic electrolyte development remains in its early stages. Herein, we report the preparation and potential application of a high-performance covalent organic framework (COF)-based protonic electrolyte for solid-state proton batteries. Using a mechanochemical method, H3PO4 was incorporated into the channels of a sulfonated COF (COF-SO3H) to produce the composite solid-state electrolyte, H3PO4@COF-SO3H. This composite was thoroughly characterized using techniques such as powder X-ray diffraction, 13C NMR spectroscopy, X-ray photoelectron spectroscopy, and nitrogen adsorption/desorption analysis. Impedance spectroscopy revealed that H3PO4@COF-SO3H exhibited superprotonic conductivity exceeding 10-2 S cm-1 under ambient conditions, alongside remarkable long-term stability and a broad electrochemical stability window. A solid-state proton battery assembled using H3PO4@COF-SO3H as the electrolyte demonstrated exceptional performance, including excellent rate capability, high specific capacity of 101.8 mAh g-1 at 1.0 A g-1, and good cycling stability with a capacity retention of 80.6% after 1000 cycles at 1.0 A g-1, outperforming previously reported solid-state proton batteries. These findings suggest that COF-based composite solid-state electrolytes hold significant promise for future applications in solid-state proton batteries.
固态质子电池是一种新兴的有前途的能源存储技术。然而,高效固态质子电解质的发展仍处于早期阶段。本文报道了一种基于共价有机骨架(COF)的高性能固态质子电池质子电解质的制备及其潜在应用。采用机械化学方法,将H3PO4掺入磺化COF (COF- so3h)的通道中,制备复合固态电解质H3PO4@COF-SO3H。利用粉末x射线衍射、13C核磁共振波谱、x射线光电子能谱和氮吸附/解吸分析等技术对该复合材料进行了全面表征。阻抗谱分析表明,H3PO4@COF-SO3H在环境条件下具有超过10-2 S cm-1的超质子导电性,具有显著的长期稳定性和较宽的电化学稳定性窗口。使用H3PO4@COF-SO3H作为电解液组装的固态质子电池表现出优异的性能,包括出色的倍率能力,1.0 A g-1时101.8 mAh g-1的高比容量,以及良好的循环稳定性,在1.0 A g-1下循环1000次后容量保持率为80.6%,优于先前报道的固态质子电池。这些发现表明,基于cof的复合固态电解质在固态质子电池的未来应用中具有重要的前景。
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.