Minhee Lee, Soyoung Kim, Chanho Yuk, Gyeongdoo Kang, Euimin Lee, Han-Hee Cho, Sung Yun Son, Woochul Song, Taesu Kim, Wonho Lee
{"title":"锂离子电池高容量NDI聚合物负极后处理策略","authors":"Minhee Lee, Soyoung Kim, Chanho Yuk, Gyeongdoo Kang, Euimin Lee, Han-Hee Cho, Sung Yun Son, Woochul Song, Taesu Kim, Wonho Lee","doi":"10.1002/cssc.202501246","DOIUrl":null,"url":null,"abstract":"<p><p>Conjugated polymer cathodes are promising candidates for next-generation Li-ion batteries, but their practical application is limited by the presence of inactive alkyl side chains that reduce specific capacity. A simple heat-treatment strategy is reported to selectively remove the alkyl side chains of a naphthalenediimide (NDI)-based polymer, P(NDI2OD-T2), an n-type conjugated polymer, resulting in a nearly twofold increase in specific capacity, from 56.3 mAh g<sup>-1</sup> (fresh) to 117.0 mAh g<sup>-1</sup> (heat-treated). Thermogravimetric analysis and gas chromatography-mass spectrometry confirmed the selective cleavage of alkyl groups at 420 °C without significant degradation of the polymer backbone. The resulting porous architecture, verified by Brunauer-Emmett-Teller and scanning electron microscopy analyses, promoted ion diffusion and enhanced the capacitive contribution to charge storage. Electrochemical measurements revealed that the heat-treated cathode exhibited excellent performance at sub-zero temperatures, attributed to improved ion transport and surface-driven storage mechanisms. In contrast, the fresh electrode retained higher electronic conductivity and superior rate capability at room temperature, due to its preserved crystallinity. These findings provide mechanistic insight into how post-processing can modulate the structure-property relationship of conjugated polymer cathodes and offer a versatile and practical approach toward improving specific capacity in organic electrode materials.</p>","PeriodicalId":149,"journal":{"name":"ChemSusChem","volume":" ","pages":"e202501246"},"PeriodicalIF":6.6000,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Post-Treatment Strategy for High-Capacity Naphtalenediimide (NDI) Polymer Cathodes in Li-Ion Batteries.\",\"authors\":\"Minhee Lee, Soyoung Kim, Chanho Yuk, Gyeongdoo Kang, Euimin Lee, Han-Hee Cho, Sung Yun Son, Woochul Song, Taesu Kim, Wonho Lee\",\"doi\":\"10.1002/cssc.202501246\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Conjugated polymer cathodes are promising candidates for next-generation Li-ion batteries, but their practical application is limited by the presence of inactive alkyl side chains that reduce specific capacity. A simple heat-treatment strategy is reported to selectively remove the alkyl side chains of a naphthalenediimide (NDI)-based polymer, P(NDI2OD-T2), an n-type conjugated polymer, resulting in a nearly twofold increase in specific capacity, from 56.3 mAh g<sup>-1</sup> (fresh) to 117.0 mAh g<sup>-1</sup> (heat-treated). Thermogravimetric analysis and gas chromatography-mass spectrometry confirmed the selective cleavage of alkyl groups at 420 °C without significant degradation of the polymer backbone. The resulting porous architecture, verified by Brunauer-Emmett-Teller and scanning electron microscopy analyses, promoted ion diffusion and enhanced the capacitive contribution to charge storage. Electrochemical measurements revealed that the heat-treated cathode exhibited excellent performance at sub-zero temperatures, attributed to improved ion transport and surface-driven storage mechanisms. In contrast, the fresh electrode retained higher electronic conductivity and superior rate capability at room temperature, due to its preserved crystallinity. These findings provide mechanistic insight into how post-processing can modulate the structure-property relationship of conjugated polymer cathodes and offer a versatile and practical approach toward improving specific capacity in organic electrode materials.</p>\",\"PeriodicalId\":149,\"journal\":{\"name\":\"ChemSusChem\",\"volume\":\" \",\"pages\":\"e202501246\"},\"PeriodicalIF\":6.6000,\"publicationDate\":\"2025-09-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ChemSusChem\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/cssc.202501246\",\"RegionNum\":2,\"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":"ChemSusChem","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/cssc.202501246","RegionNum":2,"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
共轭聚合物阴极是下一代锂离子电池的理想选择,但其实际应用受到非活性烷基侧链的限制,降低了比容量。据报道,一种简单的热处理策略可以选择性地去除萘二亚胺(NDI)基聚合物P(NDI2OD-T2)的烷基侧链,这是一种n型共轭聚合物,其比容量增加了近两倍,从56.3 mAh g-1(新鲜)增加到117.0 mAh g-1(热处理)。热重分析和气相色谱-质谱分析证实了在420°C下烷基的选择性裂解,而聚合物主链没有明显的降解。由此产生的多孔结构,经brunauer - emmet - teller和扫描电子显微镜分析证实,促进了离子扩散并增强了电荷存储的电容性贡献。电化学测量表明,经过热处理的阴极在零下温度下表现出优异的性能,这归因于离子传输和表面驱动的存储机制的改善。相比之下,由于保持了结晶度,新鲜电极在室温下保持了更高的电子导电性和优越的速率能力。这些发现为后处理如何调节共轭聚合物阴极的结构-性能关系提供了机制见解,并为提高有机电极材料的比容量提供了一种通用和实用的方法。
Post-Treatment Strategy for High-Capacity Naphtalenediimide (NDI) Polymer Cathodes in Li-Ion Batteries.
Conjugated polymer cathodes are promising candidates for next-generation Li-ion batteries, but their practical application is limited by the presence of inactive alkyl side chains that reduce specific capacity. A simple heat-treatment strategy is reported to selectively remove the alkyl side chains of a naphthalenediimide (NDI)-based polymer, P(NDI2OD-T2), an n-type conjugated polymer, resulting in a nearly twofold increase in specific capacity, from 56.3 mAh g-1 (fresh) to 117.0 mAh g-1 (heat-treated). Thermogravimetric analysis and gas chromatography-mass spectrometry confirmed the selective cleavage of alkyl groups at 420 °C without significant degradation of the polymer backbone. The resulting porous architecture, verified by Brunauer-Emmett-Teller and scanning electron microscopy analyses, promoted ion diffusion and enhanced the capacitive contribution to charge storage. Electrochemical measurements revealed that the heat-treated cathode exhibited excellent performance at sub-zero temperatures, attributed to improved ion transport and surface-driven storage mechanisms. In contrast, the fresh electrode retained higher electronic conductivity and superior rate capability at room temperature, due to its preserved crystallinity. These findings provide mechanistic insight into how post-processing can modulate the structure-property relationship of conjugated polymer cathodes and offer a versatile and practical approach toward improving specific capacity in organic electrode materials.
期刊介绍:
ChemSusChem
Impact Factor (2016): 7.226
Scope:
Interdisciplinary journal
Focuses on research at the interface of chemistry and sustainability
Features the best research on sustainability and energy
Areas Covered:
Chemistry
Materials Science
Chemical Engineering
Biotechnology