Jun Shen , Shilin Zhang , Haoli Wang , Renxin Wang , Yingying Hu , Yiyang Mao , Ruilin Wang , Huihui Zhang , Yumeng Du , Yameng Fan , Yingtang Zhou , Zaiping Guo , Baofeng Wang
{"title":"释放硅阳极在锂离子电池中的潜力:具有协同界面键合作用的爪启发粘合剂","authors":"Jun Shen , Shilin Zhang , Haoli Wang , Renxin Wang , Yingying Hu , Yiyang Mao , Ruilin Wang , Huihui Zhang , Yumeng Du , Yameng Fan , Yingtang Zhou , Zaiping Guo , Baofeng Wang","doi":"10.1016/j.esci.2023.100207","DOIUrl":null,"url":null,"abstract":"<div><p>Binders play a crucial role in enhancing the cycling stability of silicon anodes in next-generation Li-ion batteries. However, traditional linear polymer binders have difficulty withstanding the volume expansion of silicon during cycling. Herein, inspired by the fact that animals’ claws can grasp objects firmly, a claw-like taurine-grafted-poly (acrylic acid) binder (Tau-g-PAA) is designed to improve the electrochemical performance of silicon anodes. The synergistic effects of different polar groups (sulfo and carboxyl) in Tau-g-PAA facilitate the formation of multidimensional interactions with silicon nanoparticles and the diffusion of Li ions, thereby greatly improving the stability and rate performance of silicon anodes, which aligns with results from density functional theory (DFT) simulations. As expected, a Tau-g-PAA/Si electrode exhibits excellent cycling performance with a high specific capacity of 1003 mA h g<sup>−1</sup> at 1 C (1 C = 4200 mA h g<sup>−1</sup>) after 300 cycles, and a high rate performance. The design strategy of using polar small molecule-grafted polymers to create claw-like structures could inspire the development of better binders for silicon-based anodes.</p></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"4 3","pages":"Article 100207"},"PeriodicalIF":42.9000,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667141723001532/pdfft?md5=2a5d850efe52e6935ff0d1d0541f4a19&pid=1-s2.0-S2667141723001532-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Unlocking the potential of silicon anodes in lithium-ion batteries: A claw-inspired binder with synergistic interface bonding\",\"authors\":\"Jun Shen , Shilin Zhang , Haoli Wang , Renxin Wang , Yingying Hu , Yiyang Mao , Ruilin Wang , Huihui Zhang , Yumeng Du , Yameng Fan , Yingtang Zhou , Zaiping Guo , Baofeng Wang\",\"doi\":\"10.1016/j.esci.2023.100207\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Binders play a crucial role in enhancing the cycling stability of silicon anodes in next-generation Li-ion batteries. However, traditional linear polymer binders have difficulty withstanding the volume expansion of silicon during cycling. Herein, inspired by the fact that animals’ claws can grasp objects firmly, a claw-like taurine-grafted-poly (acrylic acid) binder (Tau-g-PAA) is designed to improve the electrochemical performance of silicon anodes. The synergistic effects of different polar groups (sulfo and carboxyl) in Tau-g-PAA facilitate the formation of multidimensional interactions with silicon nanoparticles and the diffusion of Li ions, thereby greatly improving the stability and rate performance of silicon anodes, which aligns with results from density functional theory (DFT) simulations. As expected, a Tau-g-PAA/Si electrode exhibits excellent cycling performance with a high specific capacity of 1003 mA h g<sup>−1</sup> at 1 C (1 C = 4200 mA h g<sup>−1</sup>) after 300 cycles, and a high rate performance. The design strategy of using polar small molecule-grafted polymers to create claw-like structures could inspire the development of better binders for silicon-based anodes.</p></div>\",\"PeriodicalId\":100489,\"journal\":{\"name\":\"eScience\",\"volume\":\"4 3\",\"pages\":\"Article 100207\"},\"PeriodicalIF\":42.9000,\"publicationDate\":\"2024-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2667141723001532/pdfft?md5=2a5d850efe52e6935ff0d1d0541f4a19&pid=1-s2.0-S2667141723001532-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"eScience\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2667141723001532\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ELECTROCHEMISTRY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"eScience","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667141723001532","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
摘要
粘合剂在提高下一代锂离子电池中硅阳极的循环稳定性方面起着至关重要的作用。然而,传统的线性聚合物粘合剂很难承受硅在循环过程中的体积膨胀。受动物爪子能牢牢抓住物体的启发,本文设计了一种类似爪子的牛磺酸接枝聚丙烯酸粘合剂(Tau-g-PAA),以改善硅阳极的电化学性能。Tau-g-PAA 中不同极性基团(磺基和羧基)的协同作用促进了与硅纳米颗粒形成多维相互作用以及锂离子的扩散,从而大大提高了硅阳极的稳定性和速率性能,这与密度泛函理论(DFT)模拟的结果一致。正如预期的那样,Tau-g-PAA/Si 电极表现出优异的循环性能,在 1 C(1 C = 4200 mA h g-1)条件下循环 300 次后,比容量高达 1003 mA h g-1,并且具有很高的速率性能。使用极性小分子接枝聚合物创建爪状结构的设计策略可为硅基阳极开发更好的粘合剂提供启发。
Unlocking the potential of silicon anodes in lithium-ion batteries: A claw-inspired binder with synergistic interface bonding
Binders play a crucial role in enhancing the cycling stability of silicon anodes in next-generation Li-ion batteries. However, traditional linear polymer binders have difficulty withstanding the volume expansion of silicon during cycling. Herein, inspired by the fact that animals’ claws can grasp objects firmly, a claw-like taurine-grafted-poly (acrylic acid) binder (Tau-g-PAA) is designed to improve the electrochemical performance of silicon anodes. The synergistic effects of different polar groups (sulfo and carboxyl) in Tau-g-PAA facilitate the formation of multidimensional interactions with silicon nanoparticles and the diffusion of Li ions, thereby greatly improving the stability and rate performance of silicon anodes, which aligns with results from density functional theory (DFT) simulations. As expected, a Tau-g-PAA/Si electrode exhibits excellent cycling performance with a high specific capacity of 1003 mA h g−1 at 1 C (1 C = 4200 mA h g−1) after 300 cycles, and a high rate performance. The design strategy of using polar small molecule-grafted polymers to create claw-like structures could inspire the development of better binders for silicon-based anodes.