Covalent-Organic Framework with Superior Proton Conduction for Solid-State Proton Battery Application

被引:0
作者
Ren, Xing-Yu [1 ,2 ]
Song, Jing-Bo [1 ,2 ]
Zhang, Guo-Qin [1 ,2 ]
Kong, Ya-Ru [1 ,2 ]
Zhang, Han [1 ,2 ]
Qiao, Qiao [1 ,2 ]
Luo, Hong-Bin [1 ,2 ]
Zhang, Jin [1 ,2 ]
Liu, Jian-Lan [1 ,2 ]
Ren, Xiao-Ming [1 ,2 ,3 ,4 ]
机构
[1] Nanjing Tech Univ, State Key Lab Mat Oriented Chem Engn, Nanjing 211816, Peoples R China
[2] Nanjing Tech Univ, Coll Chem & Mol Engn, Nanjing 211816, Peoples R China
[3] Nanjing Tech Univ, Coll Mat Sci & Engn, Nanjing 211816, Peoples R China
[4] Nanjing Univ, State Key Lab Coordinat Chem, Nanjing 210023, Peoples R China
来源
ACS MATERIALS LETTERS | 2024年 / 6卷 / 09期
基金
中国国家自然科学基金;
关键词
ACID;
D O I
10.1021/acsmaterialslett.4c01140
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Solid-state proton batteries hold great promise as a technology for portable energy storage. However, their development is impeded by the scarcity of suitable solid proton electrolytes. In this study, we present the first demonstration of covalent-organic frameworks (COFs) exploited as solid proton electrolytes with promising application in solid-state proton batteries. Specifically, the methanesulfonic acid (MeSA) molecules were confined and stabilized within the channels of a polybenzimidazole COF (PBI-COF) to yield the solid proton electrolyte, termed MeSA@PBI-COF. MeSA@PBI-COF exhibits a wide electrochemical stability window and superior proton conduction (>10(-2 )S cm(-1)) under ambient conditions, along with good long-term stability. Furthermore, MeSA@PBI-COF was employed as the solid proton electrolyte to assemble solid-state proton batteries, which demonstrate excellent cycle stability with a capacity retention of 74.2% after 8000 cycles at 1.0 A g(-1) and deliver a high specific capacity of 49.8 mAh g(-1) at 1.0 A g(-1), outperforming the reported solid-state proton batteries.
引用
收藏
页码:4036 / 4041
页数:6
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