Redox-active poly(imide-quinone) covalent organic framework anodes for high-efficient and durable aqueous proton batteries

被引:1
|
作者
Miao, Yao [1 ]
Jin, Wei [1 ]
Qin, Mengna [1 ]
Shen, Yong-Miao [2 ]
Chen, Yanli [1 ]
Wu, Tai-Rui [3 ,4 ]
Wu, De-Yin [1 ]
Xu, Juan [1 ]
Cao, Jianyu [1 ]
机构
[1] Changzhou Univ, Sch Petrochem Engn, Jiangsu Key Lab Adv Catalyt Mat & Technol, Changzhou 213164, Jiangsu, Peoples R China
[2] Zhejiang Sci Tech Univ, Sch Chem & Chem Engn, Hangzhou 310018, Peoples R China
[3] Xiamen Univ, Coll Chem & Chem Engn, State Key Lab Phys Chem Solid Surface, Xiamen 361005, Peoples R China
[4] Xiamen Univ, Coll Chem & Chem Engn, Dept Chem, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金;
关键词
Proton battery; Covalent organic framework; Anode material; Poly(imide-quinone); Copper hexacyanoferrate; PHASE;
D O I
10.1016/j.cej.2024.149986
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Hydrogen ions (protons), as the lightest and smallest non-metallic charge carriers, have aroused great interest in the field of aqueous batteries. Unfortunately, most anode materials used for these proton batteries still suffer from low specific capacity and/or unsatisfactory cycle durability due to structural deterioration resulted from corrosion of strong acid electrolytes. Here, we report for the first time a robust poly(imide-quinone) (PIQ) covalent organic framework (COF) with dual redox-active naphthalene diimide-paraquinone motifs in its periodic skeletons for proton storage, which can afford a high reversible capacity of similar to 255.6 mAh/g at a current density of 1 A/g with outstanding cycling stability. The aqueous proton battery (APB) fabricated with this PIQ-COF anode and a copper hexacyanoferrate (CuHCF) cathode demonstrates an unprecedentedly remarkable combination of reversible capacity (about 138 mAh/g at 0.5 A/g), rate capability (76.5 % capacity retention at 20 A/g), and long-term cyclability (99.999 % per cycle for 10,000 cycles at 3 A/g). The ex situ FTIR characterization reveals that the C = O groups in naphthalene imides and paraquinones contribute abundant and accessible redox-active sites for proton storage.
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页数:10
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