{"title":"高倍率容量锂离子电池的快速反应动力学π-桥联离子共价有机骨架。","authors":"Ju Duan,Feng Chen,Huajie Yu,Shenbo Zhu,Likuan Teng,Kexiang Wang,Tiejun Chen,Wei Lyu,Huawei Hu,Yaozu Liao","doi":"10.1002/anie.202505207","DOIUrl":null,"url":null,"abstract":"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 π-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 10000 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 for high-rate performance, paving the way for next-generation energy storage technologies.","PeriodicalId":125,"journal":{"name":"Angewandte Chemie International Edition","volume":"9 1","pages":"e202505207"},"PeriodicalIF":16.1000,"publicationDate":"2025-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"π-Bridge Linked Ionic Covalent Organic Framework with Fast Reaction Kinetics for High-Rate-Capacity Lithium Ion Batteries.\",\"authors\":\"Ju Duan,Feng Chen,Huajie Yu,Shenbo Zhu,Likuan Teng,Kexiang Wang,Tiejun Chen,Wei Lyu,Huawei Hu,Yaozu Liao\",\"doi\":\"10.1002/anie.202505207\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"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 π-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 10000 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 for high-rate performance, paving the way for next-generation energy storage technologies.\",\"PeriodicalId\":125,\"journal\":{\"name\":\"Angewandte Chemie International Edition\",\"volume\":\"9 1\",\"pages\":\"e202505207\"},\"PeriodicalIF\":16.1000,\"publicationDate\":\"2025-05-19\",\"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.202505207\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie International Edition","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/anie.202505207","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
摘要
共价有机框架(COFs)由于其良好的拓扑结构和可调的孔隙结构而成为高性能锂离子电池(lib)的极具前景的正极材料。然而,它们的实际应用往往受到本质上缓慢的电荷转移和较差的反应动力学的限制。为了解决这些问题,我们通过与三唑离子液体的一锅波瓦洛夫反应,开发了一种离子喹啉连接COF (iQCOF)阴极。iQCOF结构通过整合π桥诱导的电荷离域以促进电荷传输,特定吸附效应以获得快速的离子气氛解离速率,极性三嗪单元以实现稳定界面的均匀离子通量,从而实现协同增强。因此,iQCOF提供了407 mAh g-1的高比容量,701 Wh kg-1,以及卓越的倍率能力(121 mAh g-1, 10 a g-1),每周期0.0027%,超过10000次循环,进一步突出了其作为高性能有机阴极的潜力。这项工作为先进的基于cof的阴极提供了一种方便的策略,具有快速反应动力学的高速率性能,为下一代储能技术铺平了道路。
π-Bridge Linked Ionic Covalent Organic Framework with Fast Reaction Kinetics for High-Rate-Capacity Lithium Ion Batteries.
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 π-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 10000 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 for high-rate performance, paving the way for next-generation energy storage technologies.
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.