In Situ Polymerized Polyfluorinated Crosslinked Polyether Electrolytes for High-Voltage Lithium Metal Batteries

IF 27.4 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Shimei Li, Hu Hong, Xinru Yang, Dedi Li, Qi Xiong, Dechao Zhang, Shixun Wang, Zhaodong Huang, Haiming Lv, Chunyi Zhi
{"title":"In Situ Polymerized Polyfluorinated Crosslinked Polyether Electrolytes for High-Voltage Lithium Metal Batteries","authors":"Shimei Li, Hu Hong, Xinru Yang, Dedi Li, Qi Xiong, Dechao Zhang, Shixun Wang, Zhaodong Huang, Haiming Lv, Chunyi Zhi","doi":"10.1002/adma.202504333","DOIUrl":null,"url":null,"abstract":"In situ polymerized polyether electrolytes are promising for solid-state Li metal batteries due to their high ionic conductivity and excellent interfacial contact. However, their practical application is hindered by Li dendrite formation, interfacial degradation, and limited oxidative stability. Herein, we propose an in situ polymerized polyfluorinated crosslinked polyether electrolyte (PDOL-OFHDBO), synthesized by copolymerizing 1,3-dioxolane (DOL) with 2,2′-(2,2,3,3,4,4,5,5-octafluorohexane-1,6-diyl)bis(oxirane) (OFHDBO) as a polyfluorinated crosslinker. The electron-withdrawing polyfluorinated groups endow PDOL-OFHDBO with enhanced oxidative stability and interfacial compatibility, while reducing the solvation power of the polymer matrix to promote an anion-derived inorganic-rich solid electrolyte interphase for uniform Li deposition. Consequently, PDOL-OFHDBO exhibits a wide electrochemical stability window (&gt;5.6 V) and enables long-term stable Li plating/stripping for over 1100 h. Furthermore, Li||LiNi<sub>0.8</sub>Co<sub>0.1</sub>Mn<sub>0.1</sub>O<sub>2</sub> (NCM811) full cells utilizing PDOL-OFHDBO demonstrate outstanding cycling stability with high-loading cathodes (≈3.8 mAh cm<sup>−2</sup>) and thin Li anodes (50 µm), achieving capacity retention of 95.5% and 89.1% over 100 cycles at cut-off voltages of 4.3 and 4.5 V, respectively. Remarkably, Ah-level Li||NCM811 pouch cells deliver an impressive specific energy of 401.8 Wh kg<sup>−1</sup>, highlighting their potential for practical solid-state Li metal batteries.","PeriodicalId":114,"journal":{"name":"Advanced Materials","volume":"21 1","pages":""},"PeriodicalIF":27.4000,"publicationDate":"2025-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adma.202504333","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

In situ polymerized polyether electrolytes are promising for solid-state Li metal batteries due to their high ionic conductivity and excellent interfacial contact. However, their practical application is hindered by Li dendrite formation, interfacial degradation, and limited oxidative stability. Herein, we propose an in situ polymerized polyfluorinated crosslinked polyether electrolyte (PDOL-OFHDBO), synthesized by copolymerizing 1,3-dioxolane (DOL) with 2,2′-(2,2,3,3,4,4,5,5-octafluorohexane-1,6-diyl)bis(oxirane) (OFHDBO) as a polyfluorinated crosslinker. The electron-withdrawing polyfluorinated groups endow PDOL-OFHDBO with enhanced oxidative stability and interfacial compatibility, while reducing the solvation power of the polymer matrix to promote an anion-derived inorganic-rich solid electrolyte interphase for uniform Li deposition. Consequently, PDOL-OFHDBO exhibits a wide electrochemical stability window (>5.6 V) and enables long-term stable Li plating/stripping for over 1100 h. Furthermore, Li||LiNi0.8Co0.1Mn0.1O2 (NCM811) full cells utilizing PDOL-OFHDBO demonstrate outstanding cycling stability with high-loading cathodes (≈3.8 mAh cm−2) and thin Li anodes (50 µm), achieving capacity retention of 95.5% and 89.1% over 100 cycles at cut-off voltages of 4.3 and 4.5 V, respectively. Remarkably, Ah-level Li||NCM811 pouch cells deliver an impressive specific energy of 401.8 Wh kg−1, highlighting their potential for practical solid-state Li metal batteries.

Abstract Image

高压锂金属电池用原位聚合多氟交联聚醚电解质
原位聚合聚醚电解质具有高离子电导率和良好的界面接触性能,在固态锂金属电池中具有广阔的应用前景。然而,它们的实际应用受到锂枝晶形成、界面降解和有限的氧化稳定性的阻碍。本文提出了一种原位聚合多氟交联聚醚电解质(pdolo -OFHDBO),该电解质由1,3-二恶烷(DOL)与2,2 ' -(2,2,3,3,3,4,4,5,5 -辛氟己烷-1,6-二基)双氧环烷(OFHDBO)作为多氟交联剂共聚而成。吸电子的多氟基团赋予pdolo - ofhdbo增强的氧化稳定性和界面相容性,同时降低聚合物基体的溶剂化能力,促进阴离子衍生的富无机固体电解质界面相均匀沉积锂。因此,pdolo - ofhdbo表现出宽的电化学稳定窗口(>5.6 V),能够长期稳定地镀/剥离超过1100小时。此外,使用pdolo - ofhdbo的Li||LiNi0.8Co0.1Mn0.1O2 (NCM811)全电池在高负载阴极(≈3.8 mAh cm - 2)和薄锂阳极(50µm)下表现出出色的循环稳定性,在4.3 V和4.5 V的截止电压下,在100次循环中分别实现了95.5%和89.1%的容量保持。值得注意的是,ah级Li||NCM811袋状电池提供了令人印象深刻的401.8 Wh kg−1的比能量,突出了它们作为实用固态锂金属电池的潜力。
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 求助全文
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.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信