{"title":"An esterified cross-linked polymer binder for high-rate stabilised silicon anodes in Lithium-Ion batteries","authors":"Lingbin Liu, Haiyan Guo, Yuxiu Yu, Qiang Zhang, Yaodong Liu, Nanwen Li","doi":"10.1016/j.electacta.2025.145824","DOIUrl":null,"url":null,"abstract":"Silicon is renowned for its high theoretical capacity as an anode material in lithium-ion batteries, yet its extensive volume changes during charge and discharge cycles pose significant challenges to its commercial viability. This study addresses these issues by developing composite binders that mitigate mechanical stresses and restrict silicon expansion. We utilize guar gum, a natural polysaccharide, and polyacrylic acid, a linear polymer, to create a cross-linked binder through condensation reactions between hydroxyl and carboxyl groups. This cross-linked structure enhances the mechanical properties of the binder, effectively suppresses the volume expansion of silicon particles, and greatly improves the cycling performance of the silicon electrode. At the same time, the electrodes obtain excellent high-rate performance profit from their high lithium ion diffusion coefficient. Samples with different degrees of cross-linking are obtained by treating the electrodes at different temperatures. The results prove and highlight the critical role of cross-linking in binder performances. Notably, the half-cell retains a specific capacity of 1500 mAh/g after 500 cycles at a high current density of 6 A/g (1 C=4.2 A/g) and 1709.8 mAh/g at a very high current density of 21 A/g (corresponding to 5 C). The full cell using Ni<sub>0.8</sub>Co<sub>0.1</sub>Mn<sub>0.1</sub>O<sub>2</sub> (NCM811) has a specific capacity of 113.3 mAh/g at 5 C, demonstrating significant potential for practical applications.","PeriodicalId":305,"journal":{"name":"Electrochimica Acta","volume":"64 1","pages":""},"PeriodicalIF":5.5000,"publicationDate":"2025-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochimica Acta","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.electacta.2025.145824","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
Silicon is renowned for its high theoretical capacity as an anode material in lithium-ion batteries, yet its extensive volume changes during charge and discharge cycles pose significant challenges to its commercial viability. This study addresses these issues by developing composite binders that mitigate mechanical stresses and restrict silicon expansion. We utilize guar gum, a natural polysaccharide, and polyacrylic acid, a linear polymer, to create a cross-linked binder through condensation reactions between hydroxyl and carboxyl groups. This cross-linked structure enhances the mechanical properties of the binder, effectively suppresses the volume expansion of silicon particles, and greatly improves the cycling performance of the silicon electrode. At the same time, the electrodes obtain excellent high-rate performance profit from their high lithium ion diffusion coefficient. Samples with different degrees of cross-linking are obtained by treating the electrodes at different temperatures. The results prove and highlight the critical role of cross-linking in binder performances. Notably, the half-cell retains a specific capacity of 1500 mAh/g after 500 cycles at a high current density of 6 A/g (1 C=4.2 A/g) and 1709.8 mAh/g at a very high current density of 21 A/g (corresponding to 5 C). The full cell using Ni0.8Co0.1Mn0.1O2 (NCM811) has a specific capacity of 113.3 mAh/g at 5 C, demonstrating significant potential for practical applications.
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.