Qiong Luo, Dongyang Zhang, Lucheng Li, Renjie Peng, Suqin Liu and Jun Chen*,
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Consequently, the TFPB-NiPc@CC electrode not only shows improved electrochemical behaviors of high capacity and long cycle stability but also displays superior flexibility and folding stability. The specific capacity achieved by the TFPB-NiPc@CC electrode is 1090.2 mA h/g at 200 mA/g, and after 500 cycles, the specific capacity of the TFPB-NiPc@CC electrode can also be maintained at 994.5 mA h/g with a retention ratio of 91.2%, which are all much higher than those of the TFPB-NiPc electrode. Moreover, TFPB-NiPc@CC also shows a high specific capacity and stable cycling behaviors in Na-ion batteries. The strategies designed in this work provide new ideas and methods for preparing practical, high-performance flexible organic anode materials.</p>","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"17 10","pages":"15398–15412 15398–15412"},"PeriodicalIF":8.2000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"In Situ Composites of Phthalocyanine-Based Covalent Organic Frameworks with Carbon Cloth as a Flexible Binder-Free Anode Material for High-Performance Lithium/Sodium-Ion Batteries\",\"authors\":\"Qiong Luo, Dongyang Zhang, Lucheng Li, Renjie Peng, Suqin Liu and Jun Chen*, \",\"doi\":\"10.1021/acsami.4c2089110.1021/acsami.4c20891\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >In situ Schiff base reaction is utilized to grow phthalocyanine covalent organic frameworks (TFPB-NiPc) on carbon cloth (CC) to obtain the composite material TFPB-NiPc@CC, which is used as the anode for the binder and conductive agent free Li/Na-ion batteries with enhanced active materials loading. 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引用次数: 0
摘要
利用原位席夫碱反应在碳布(CC)上生长酞菁共价有机骨架(TFPB-NiPc),得到复合材料TFPB-NiPc@CC,该复合材料用作无粘结剂和导电剂的锂/钠离子电池的阳极,增强了活性材料的负载。此外,CC作为优良的导电骨架,减少了酞菁框架(Pc-COFs)的堆叠效应,使TFPB-NiPc在原位合成过程中实现了自剥离效应。该策略缩短了Li+的迁移路径,有效地提高了Li+在电极中的迁移速率。结果表明,TFPB-NiPc@CC电极不仅表现出高容量、长周期稳定的电化学性能,而且表现出优异的柔韧性和折叠稳定性。在200 mA/g下,TFPB-NiPc@CC电极的比容量为1090.2 mA h/g,循环500次后,TFPB-NiPc@CC电极的比容量也能保持在994.5 mA h/g,保持率为91.2%,均远高于TFPB-NiPc电极。此外,TFPB-NiPc@CC在钠离子电池中也表现出高比容量和稳定的循环行为。本工作设计的策略为制备实用、高性能的柔性有机阳极材料提供了新的思路和方法。
In Situ Composites of Phthalocyanine-Based Covalent Organic Frameworks with Carbon Cloth as a Flexible Binder-Free Anode Material for High-Performance Lithium/Sodium-Ion Batteries
In situ Schiff base reaction is utilized to grow phthalocyanine covalent organic frameworks (TFPB-NiPc) on carbon cloth (CC) to obtain the composite material TFPB-NiPc@CC, which is used as the anode for the binder and conductive agent free Li/Na-ion batteries with enhanced active materials loading. What is more, CC acts as an excellent conductive backbone while reducing the stacking effect of phthalocyanine frameworks (Pc-COFs), which enables TFPB-NiPc to realize the self-exfoliation effect during the in situ synthesis process. This strategy shortens the migration path of Li+, efficiently resulting in improving the migration rate of Li+ in the electrode. Consequently, the TFPB-NiPc@CC electrode not only shows improved electrochemical behaviors of high capacity and long cycle stability but also displays superior flexibility and folding stability. The specific capacity achieved by the TFPB-NiPc@CC electrode is 1090.2 mA h/g at 200 mA/g, and after 500 cycles, the specific capacity of the TFPB-NiPc@CC electrode can also be maintained at 994.5 mA h/g with a retention ratio of 91.2%, which are all much higher than those of the TFPB-NiPc electrode. Moreover, TFPB-NiPc@CC also shows a high specific capacity and stable cycling behaviors in Na-ion batteries. The strategies designed in this work provide new ideas and methods for preparing practical, high-performance flexible organic anode materials.
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.