{"title":"Natural Gluten Binder Enabling High‐Performance Hard Carbon Anode in Sodium‐Ion Batteries","authors":"Siyao Wu, Jinwei Zhou, Qihou Li, Feixiang Wu","doi":"10.1002/adfm.202507916","DOIUrl":null,"url":null,"abstract":"Hard carbon (HC) is gaining recognition as a prospective anode material for sodium‐ion batteries (SIBs), showing considerable promise in energy storage applications. The binder is a key determinant of the microenvironment of electrodes, which controls the charge transport and mechanical properties. Herein, the study investigates the application of Gluten (GT), a natural mesh binder, for enhancing overall properties of the HC anode. It is found that the numerous functional groups in GT quickly form hydrogen bonds with HC particles after a slight hydration, effectively improving mechanical interlocking and significantly reducing mechanical degradation during cycles. Advanced characterization in combination with theoretical simulations shows that GT reduces the dissociation energy of PF<jats:sub>6</jats:sub><jats:sup>−</jats:sup>, which promotes the formation of a thin, uniform NaF‐rich solid‐electrolyte interface (SEI) on the HC anode surface. Consequently, HC‐GT demonstrates outstanding electrochemical performance, retaining 83% of its capacity after 1000 cycles at 0.5 A g<jats:sup>−1</jats:sup> and achieving an initial coulombic efficiency of ≈88%. Moreover, the full cell demonstrates excellent cycling stability, with a capacity of 75.8 mA h g<jats:sup>−1</jats:sup> after 800 cycles at 1 C. This work underscores the significance of selecting appropriate binders to achieve high‐performance anodes, offering a new perspective for optimizing the electrochemical performance of SIBs.","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"24 1","pages":""},"PeriodicalIF":18.5000,"publicationDate":"2025-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adfm.202507916","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Hard carbon (HC) is gaining recognition as a prospective anode material for sodium‐ion batteries (SIBs), showing considerable promise in energy storage applications. The binder is a key determinant of the microenvironment of electrodes, which controls the charge transport and mechanical properties. Herein, the study investigates the application of Gluten (GT), a natural mesh binder, for enhancing overall properties of the HC anode. It is found that the numerous functional groups in GT quickly form hydrogen bonds with HC particles after a slight hydration, effectively improving mechanical interlocking and significantly reducing mechanical degradation during cycles. Advanced characterization in combination with theoretical simulations shows that GT reduces the dissociation energy of PF6−, which promotes the formation of a thin, uniform NaF‐rich solid‐electrolyte interface (SEI) on the HC anode surface. Consequently, HC‐GT demonstrates outstanding electrochemical performance, retaining 83% of its capacity after 1000 cycles at 0.5 A g−1 and achieving an initial coulombic efficiency of ≈88%. Moreover, the full cell demonstrates excellent cycling stability, with a capacity of 75.8 mA h g−1 after 800 cycles at 1 C. This work underscores the significance of selecting appropriate binders to achieve high‐performance anodes, offering a new perspective for optimizing the electrochemical performance of SIBs.
硬碳(HC)作为钠离子电池(sib)的极具前景的负极材料,在储能应用中显示出相当大的前景。粘合剂是电极微环境的关键决定因素,它控制着电荷输运和机械性能。在此,研究了谷蛋白(GT)的应用,一种天然的网状粘合剂,以提高HC阳极的整体性能。发现GT中大量的官能团在轻微水化后迅速与HC颗粒形成氢键,有效地改善了机械联锁,显著减少了循环过程中的机械降解。先进的表征结合理论模拟表明,GT降低了PF6−的解离能,促进了HC阳极表面薄而均匀的富NaF固体电解质界面(SEI)的形成。因此,HC‐GT表现出优异的电化学性能,在0.5 A g−1下循环1000次后仍能保持83%的容量,初始库仑效率约为88%。此外,完整的电池表现出优异的循环稳定性,在1℃下循环800次后的容量为75.8 mA h g−1。这项工作强调了选择合适的粘合剂来实现高性能阳极的重要性,为优化sib的电化学性能提供了新的视角。
期刊介绍:
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