仿生表面设计实现了高性能阳极的弹性固体电解质间相

IF 18.9 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Energy Storage Materials Pub Date : 2024-11-07 DOI:10.1016/j.ensm.2024.103871
Yue Zhai , Zhen Wei , Jiaxing He , Ziyun Zhao , Qiang Li , Yiran Jia , Qing He , Shichao Wu , Quan-Hong Yang
{"title":"仿生表面设计实现了高性能阳极的弹性固体电解质间相","authors":"Yue Zhai ,&nbsp;Zhen Wei ,&nbsp;Jiaxing He ,&nbsp;Ziyun Zhao ,&nbsp;Qiang Li ,&nbsp;Yiran Jia ,&nbsp;Qing He ,&nbsp;Shichao Wu ,&nbsp;Quan-Hong Yang","doi":"10.1016/j.ensm.2024.103871","DOIUrl":null,"url":null,"abstract":"<div><div>Surface coating presents an effective methodology for mitigating the detrimental effects of large volume changes inherent to high-capacity anode materials (e.g. Si, SiO<sub>x</sub>). However, designs often prioritize the protection of internal active particles, inadvertently neglecting the intricate interplay between the coating layer and the external electrolyte which exhibits profound influences on the solid electrolyte interphases (SEIs). Inspired by the extracellular polymeric substance (EPS) protecting biological cells (e.g. yeast) from predation and chemical damages, we prepare a conducting polymer-based EPS system (CP-EPS) on a surface bilayer comprising soft carbon membranes and compact graphene walls, constructing the biomimetic cellular structure. The CP-EPS chemically interacts with electrolyte catalyzing the symbiosis of integrated LiF-enriched SEIs and physically provide sufficient resilience for SEIs. This resilient SEIs offer excellent reaction kinetics and roughness which protects the structural integrity of the particle and itself from pulverization and excessive SEI thickening. The prepared SiO<sub>x</sub> anode delivers a superior average coulombic efficiency of 99.4 % over 200 cycles at 0.5C and a high reversible capacity of 730 mAh g<sup>-1</sup> after 300 cycles at 2C.</div></div>","PeriodicalId":306,"journal":{"name":"Energy Storage Materials","volume":"74 ","pages":"Article 103871"},"PeriodicalIF":18.9000,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Biomimetic surface design enables a resilient solid electrolyte interphase for high-performance anodes\",\"authors\":\"Yue Zhai ,&nbsp;Zhen Wei ,&nbsp;Jiaxing He ,&nbsp;Ziyun Zhao ,&nbsp;Qiang Li ,&nbsp;Yiran Jia ,&nbsp;Qing He ,&nbsp;Shichao Wu ,&nbsp;Quan-Hong Yang\",\"doi\":\"10.1016/j.ensm.2024.103871\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Surface coating presents an effective methodology for mitigating the detrimental effects of large volume changes inherent to high-capacity anode materials (e.g. Si, SiO<sub>x</sub>). However, designs often prioritize the protection of internal active particles, inadvertently neglecting the intricate interplay between the coating layer and the external electrolyte which exhibits profound influences on the solid electrolyte interphases (SEIs). Inspired by the extracellular polymeric substance (EPS) protecting biological cells (e.g. yeast) from predation and chemical damages, we prepare a conducting polymer-based EPS system (CP-EPS) on a surface bilayer comprising soft carbon membranes and compact graphene walls, constructing the biomimetic cellular structure. The CP-EPS chemically interacts with electrolyte catalyzing the symbiosis of integrated LiF-enriched SEIs and physically provide sufficient resilience for SEIs. This resilient SEIs offer excellent reaction kinetics and roughness which protects the structural integrity of the particle and itself from pulverization and excessive SEI thickening. The prepared SiO<sub>x</sub> anode delivers a superior average coulombic efficiency of 99.4 % over 200 cycles at 0.5C and a high reversible capacity of 730 mAh g<sup>-1</sup> after 300 cycles at 2C.</div></div>\",\"PeriodicalId\":306,\"journal\":{\"name\":\"Energy Storage Materials\",\"volume\":\"74 \",\"pages\":\"Article 103871\"},\"PeriodicalIF\":18.9000,\"publicationDate\":\"2024-11-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Energy Storage Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2405829724006974\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy Storage Materials","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2405829724006974","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

摘要

表面涂层是减轻大容量阳极材料(如 Si、SiOx)固有的大体积变化的有害影响的有效方法。然而,在设计中通常会优先考虑保护内部活性颗粒,却无意中忽略了涂层与外部电解质之间错综复杂的相互作用,而外部电解质对固体电解质相间层(SEIs)有着深远的影响。受保护生物细胞(如酵母)免受捕食和化学损害的胞外聚合物物质(EPS)的启发,我们在由软碳膜和致密石墨烯壁组成的表面双层上制备了基于导电聚合物的 EPS 系统(CP-EPS),构建了仿生物细胞结构。CP-EPS 与电解质发生化学作用,催化富含锂离子的集成 SEI 的共生,并为 SEI 提供足够的物理弹性。这种弹性 SEI 具有出色的反应动力学和粗糙度,可保护颗粒及其本身的结构完整性,防止粉化和 SEI 过度增厚。制备的氧化硅阳极在 0.5 摄氏度条件下循环 200 次后,平均库仑效率达到 99.4%,在 2 摄氏度条件下循环 300 次后,可逆容量达到 730 mAh g-1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Biomimetic surface design enables a resilient solid electrolyte interphase for high-performance anodes
Surface coating presents an effective methodology for mitigating the detrimental effects of large volume changes inherent to high-capacity anode materials (e.g. Si, SiOx). However, designs often prioritize the protection of internal active particles, inadvertently neglecting the intricate interplay between the coating layer and the external electrolyte which exhibits profound influences on the solid electrolyte interphases (SEIs). Inspired by the extracellular polymeric substance (EPS) protecting biological cells (e.g. yeast) from predation and chemical damages, we prepare a conducting polymer-based EPS system (CP-EPS) on a surface bilayer comprising soft carbon membranes and compact graphene walls, constructing the biomimetic cellular structure. The CP-EPS chemically interacts with electrolyte catalyzing the symbiosis of integrated LiF-enriched SEIs and physically provide sufficient resilience for SEIs. This resilient SEIs offer excellent reaction kinetics and roughness which protects the structural integrity of the particle and itself from pulverization and excessive SEI thickening. The prepared SiOx anode delivers a superior average coulombic efficiency of 99.4 % over 200 cycles at 0.5C and a high reversible capacity of 730 mAh g-1 after 300 cycles at 2C.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Energy Storage Materials
Energy Storage Materials Materials Science-General Materials Science
CiteScore
33.00
自引率
5.90%
发文量
652
审稿时长
27 days
期刊介绍: Energy Storage Materials is a global interdisciplinary journal dedicated to sharing scientific and technological advancements in materials and devices for advanced energy storage and related energy conversion, such as in metal-O2 batteries. The journal features comprehensive research articles, including full papers and short communications, as well as authoritative feature articles and reviews by leading experts in the field. Energy Storage Materials covers a wide range of topics, including the synthesis, fabrication, structure, properties, performance, and technological applications of energy storage materials. Additionally, the journal explores strategies, policies, and developments in the field of energy storage materials and devices for sustainable energy. Published papers are selected based on their scientific and technological significance, their ability to provide valuable new knowledge, and their relevance to the international research community.
期刊最新文献
Optimized molecular interactions significantly enhance capacitive energy storage in polymer blends at 150 °C A High Power Flexible Zn-Air Battery via Concurrent PAA Modulation and Structural Tuning Surface acidity regulation for boosting Li2O2 decomposition towards lower charge overpotential Li–O2 batteries “Preferential Adsorption-Decomposition and Strong Binding” Strategy-Derived Interphase Enabling Fast-Charging and Wide-Temperature Sodium Metal Batteries Unlocking Advanced Sodium Storage Performance: High-Entropy Modulates Crystallographic Sites with Reversible Multi-Electron Reaction
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1