π-Bridge-Linked Ionic Covalent Organic Framework with Fast Reaction Kinetics for High-Rate-Capacity Lithium-Ion Batteries

被引:0
作者
Duan, Ju [1 ]
Chen, Feng [1 ]
Yu, Huajie [2 ]
Zhu, Shenbo [1 ]
Teng, Likuan [1 ]
Wang, Kexiang [1 ]
Chen, Tiejun [1 ]
Lyu, Wei [1 ]
Hu, Huawei [1 ]
Liao, Yaozu [1 ]
机构
[1] Donghua Univ, Coll Mat Sci & Engn, State Key Lab Adv Fiber Mat, Shanghai 201620, Peoples R China
[2] Donghua Univ, Coll Chem & Chem Engn, State Key Lab Adv Fiber Mat, Key Lab Sci & Technol Ecotext,Minist Educ, Shanghai 201620, Peoples R China
基金
上海市自然科学基金; 中国国家自然科学基金;
关键词
Charge transfer; High reaction rate; High-rate-capacity; Ionic covalent organic framework; Specific adsorption; CATHODE MATERIALS; MODULATION; STORAGE; ENERGY;
D O I
10.1002/anie.202505207
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Covalent organic frameworks (COFs) have emerged as promising cathode materials for high-performance lithium-ion batteries (LIBs) due to their well-defined topologies and tunable pore architectures. However, their practical application is often limited by intrinsically sluggish charge transfer and inferior reaction kinetics. To address these challenges, we develop an ionic quinoline-linked COF (iQCOF) cathode via a one-pot Povarov reaction with triazole ionic liquid. The iQCOF architecture achieves a synergistic enhancement by integrating pi-bridge-induced charge delocalization to facilitate charge transport, the specific adsorption effect to gain fast ionic atmosphere dissociation rate, and polar triazine units to enable uniform ion flux for stable interfaces. As a result, iQCOF delivers a high specific capacity of 407 mAh g-1 with 701 Wh kg-1, and exceptional rate capability (121 mAh g-1 at 10 A g-1) with 0.0027% per cycle over 10 000 cycles, further highlighting its potential as a high-performance organic cathode. This work provides a convenient strategy for advanced COF-based cathodes with fast reaction kinetics to achieve high-rate performance, paving the way for next-generation energy storage technologies.
引用
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页数:10
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