Ultrafast Li-Rich Transport in Composite Solid-State Electrolytes

IF 26.8 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Advanced Materials Pub Date : 2025-01-31 DOI:10.1002/adma.202419782
Yu-Long Liao, Xi-Long Wang, Hong Yuan, Yong-Jian Li, Chun-Ming Xu, Shuai Li, Jiang-Kui Hu, Shi-Jie Yang, Fang Deng, Jia Liu, Jia-Qi Huang
{"title":"Ultrafast Li-Rich Transport in Composite Solid-State Electrolytes","authors":"Yu-Long Liao,&nbsp;Xi-Long Wang,&nbsp;Hong Yuan,&nbsp;Yong-Jian Li,&nbsp;Chun-Ming Xu,&nbsp;Shuai Li,&nbsp;Jiang-Kui Hu,&nbsp;Shi-Jie Yang,&nbsp;Fang Deng,&nbsp;Jia Liu,&nbsp;Jia-Qi Huang","doi":"10.1002/adma.202419782","DOIUrl":null,"url":null,"abstract":"<p>Solid-state lithium (Li) metal batteries (SSLMBs) have garnered considerable attention due to their potential for high energy density and intrinsic safety. However, their widespread development has been hindered by the low ionic conductivity of solid-state electrolytes. In this contribution, a novel Li-rich transport mechanism is proposed to achieve ultrafast Li-ion conduction in composite solid-state electrolytes. By incorporating cation-deficient dielectric nanofillers into polymer matrices, it is found that negatively charged cation defects effectively intensify the adsorption of Li ions, resulting in a high Li-ion concentration enrichment on the surface of fillers. More importantly, these formed Li-rich layers are interconnected to establish continuous ultrafast Li-ion transport networks. The composite electrolyte exhibited a remarkably low ion transport activation energy (0.17 eV) and achieved an unprecedented ionic conductivity of approaching 1 × 10⁻<sup>3</sup> S cm⁻<sup>1</sup> at room temperature. The Li||LiNi<sub>0.8</sub>Co<sub>0.1</sub>Mo<sub>0.1</sub>O<sub>2</sub> full cells demonstrated an extended cycling life of over 200 cycles with a capacity retention of 70.7%. This work provides a fresh insight into improving Li-ion transport by constructing interconnected Li-rich transport networks, paving the way for the development of high-performance SSLMBs.</p>","PeriodicalId":114,"journal":{"name":"Advanced Materials","volume":"37 10","pages":""},"PeriodicalIF":26.8000,"publicationDate":"2025-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Materials","FirstCategoryId":"88","ListUrlMain":"https://advanced.onlinelibrary.wiley.com/doi/10.1002/adma.202419782","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

Solid-state lithium (Li) metal batteries (SSLMBs) have garnered considerable attention due to their potential for high energy density and intrinsic safety. However, their widespread development has been hindered by the low ionic conductivity of solid-state electrolytes. In this contribution, a novel Li-rich transport mechanism is proposed to achieve ultrafast Li-ion conduction in composite solid-state electrolytes. By incorporating cation-deficient dielectric nanofillers into polymer matrices, it is found that negatively charged cation defects effectively intensify the adsorption of Li ions, resulting in a high Li-ion concentration enrichment on the surface of fillers. More importantly, these formed Li-rich layers are interconnected to establish continuous ultrafast Li-ion transport networks. The composite electrolyte exhibited a remarkably low ion transport activation energy (0.17 eV) and achieved an unprecedented ionic conductivity of approaching 1 × 10⁻3 S cm⁻1 at room temperature. The Li||LiNi0.8Co0.1Mo0.1O2 full cells demonstrated an extended cycling life of over 200 cycles with a capacity retention of 70.7%. This work provides a fresh insight into improving Li-ion transport by constructing interconnected Li-rich transport networks, paving the way for the development of high-performance SSLMBs.

Abstract Image

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
复合固态电解质的超快富锂输运。
固态锂(Li)金属电池(sslmb)由于其高能量密度和固有安全性的潜力而受到了广泛的关注。然而,固态电解质的低离子电导率阻碍了它们的广泛发展。在这篇贡献中,提出了一种新的富锂传输机制,以实现复合固态电解质中锂离子的超快传导。通过在聚合物基体中掺入缺乏阳离子的介电纳米填料,发现带负电荷的阳离子缺陷有效强化了对Li离子的吸附,导致填料表面富集了高浓度的Li离子。更重要的是,这些形成的富锂层相互连接,建立连续的超快锂离子传输网络。复合电解质表现出非常低的离子传递活化能(0.17 eV),并且在室温下达到了前所未有的接近1 × 10 S cm(毒血症)的离子电导率。Li||LiNi0.8Co0.1Mo0.1O2充满电池的循环寿命超过200次,容量保持率为70.7%。这项工作为通过构建互连的富锂传输网络来改善锂离子传输提供了新的见解,为高性能sslmb的发展铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Advanced Materials
Advanced Materials 工程技术-材料科学:综合
CiteScore
43.00
自引率
4.10%
发文量
2182
审稿时长
2 months
期刊介绍: Advanced Materials, one of the world's most prestigious journals and the foundation of the Advanced portfolio, is the home of choice for best-in-class materials science for more than 30 years. Following this fast-growing and interdisciplinary field, we are considering and publishing the most important discoveries on any and all materials from materials scientists, chemists, physicists, engineers as well as health and life scientists and bringing you the latest results and trends in modern materials-related research every week.
期刊最新文献
Ferromagnetism of Molecular Beam Epitaxy-grown Ultra-thin Cr2Ge2Te6 Films Down to the Monolayer Limit on Si Substrates. Resolving Chiral Biomolecule Mixtures via Terahertz Eigenmode-Fingerprint Circular Dichroism Spectroscopy Empowered by Achiral Gradient Metasurfaces. When Poor Exciton Dissociation Limits Photocurrents in Organic Solar Cells: Why Low Offset Non-Fullerene Acceptor Blends Can't Be Efficient. Solvent-Driven Dissolution-Regrowth-Migration Synthesis of Asymmetric Carbon Nanoparticles for Electrocatalytic Semihydrogenation. Direct Arylation Polycondensations: Emerging Protocols for the Synthesis of High-Performance Polymer Semiconductors.
×
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:604180095
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