Highly Solvating Electrolytes with Core‐Shell Solvation Structure for Lean‐Electrolyte Lithium‐Sulfur Batteries

IF 19.3 1区 材料科学 Q1 CHEMISTRY, PHYSICAL ACS Energy Letters Pub Date : 2024-11-11 DOI:10.1002/anie.202415053
Mengxue He, Lujun Zhu, Yatao Liu, Yongfeng Jia, Yizhou Hao, Guo Ye, Xufeng Hong, Zhitong Xiao, Yue Ma, Jianhao Chen, Muhammad Burhan Shafqat, Quanquan Pang
{"title":"Highly Solvating Electrolytes with Core‐Shell Solvation Structure for Lean‐Electrolyte Lithium‐Sulfur Batteries","authors":"Mengxue He, Lujun Zhu, Yatao Liu, Yongfeng Jia, Yizhou Hao, Guo Ye, Xufeng Hong, Zhitong Xiao, Yue Ma, Jianhao Chen, Muhammad Burhan Shafqat, Quanquan Pang","doi":"10.1002/anie.202415053","DOIUrl":null,"url":null,"abstract":"The practical energy density of lithium‐sulfur batteries is limited by the low sulfur utilization at lean electrolyte conditions. The highly solvating electrolytes (HSEs) promise to address the issue at harsh conditions, but the conflicting challenges of long‐term stability of radical‐mediated sulfur redox reactions (SRR) and the poor stability with lithium metal anode (LMA) have dimmed the efforts. We now present a unique core‐shell solvation structured HSE formulated with classical ether‐based solvents and phosphoramide co‐solvent. The unique core‐shell solvation structure features confinement of the phosphoramide in the first solvation shell, which prohibits severe contact reactions with LMA and endows prolonged stability for [S3]•– radical, favoring a rapid radical‐mediated solution‐based SRR. The cell with the proposed electrolyte showing a high capacity of 864 mA h gsulfur−1 under high sulfur loading of 5.5 mgsulfur cm−2 and low E/S ratio of 4 µL mgsulfur−1. The strategy further enables steady cycling of a 2.71‐A h pouch cell with a high specific energy of 307 W h kg−1. Our work highlights the fundamental chemical concept of tuning the solvation structure to simultaneously tame the SRR and LMA stability for metal‐sulfur batteries wherein the electrode reactions are heavily coupled with electrolyte chemistry.","PeriodicalId":16,"journal":{"name":"ACS Energy Letters ","volume":"95 1","pages":""},"PeriodicalIF":19.3000,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Energy Letters ","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/anie.202415053","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

Abstract

The practical energy density of lithium‐sulfur batteries is limited by the low sulfur utilization at lean electrolyte conditions. The highly solvating electrolytes (HSEs) promise to address the issue at harsh conditions, but the conflicting challenges of long‐term stability of radical‐mediated sulfur redox reactions (SRR) and the poor stability with lithium metal anode (LMA) have dimmed the efforts. We now present a unique core‐shell solvation structured HSE formulated with classical ether‐based solvents and phosphoramide co‐solvent. The unique core‐shell solvation structure features confinement of the phosphoramide in the first solvation shell, which prohibits severe contact reactions with LMA and endows prolonged stability for [S3]•– radical, favoring a rapid radical‐mediated solution‐based SRR. The cell with the proposed electrolyte showing a high capacity of 864 mA h gsulfur−1 under high sulfur loading of 5.5 mgsulfur cm−2 and low E/S ratio of 4 µL mgsulfur−1. The strategy further enables steady cycling of a 2.71‐A h pouch cell with a high specific energy of 307 W h kg−1. Our work highlights the fundamental chemical concept of tuning the solvation structure to simultaneously tame the SRR and LMA stability for metal‐sulfur batteries wherein the electrode reactions are heavily coupled with electrolyte chemistry.
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
具有核壳溶解结构的高溶解性电解质,适用于稀薄电解质锂硫电池
锂硫电池的实际能量密度受到贫电解质条件下硫利用率低的限制。高溶解度电解质(HSE)有望解决苛刻条件下的这一问题,但自由基介导的硫氧化还原反应(SRR)的长期稳定性和与锂金属负极(LMA)的稳定性差这两个相互矛盾的挑战削弱了这方面的努力。现在,我们提出了一种采用经典醚基溶剂和磷酰胺助溶剂配制的独特核壳溶解结构 HSE。这种独特的核壳溶解结构将磷酰胺限制在第一个溶解壳中,从而避免了与 LMA 发生严重的接触反应,并赋予 [S3]-- 自由基长期的稳定性,有利于以自由基为介质的快速溶液 SRR。在 5.5 mgsulfur cm-2 的高硫负荷和 4 µL mgsulfur-1 的低 E/S 比条件下,采用所建议的电解质的电池显示出 864 mA h gsulfur-1 的高容量。该策略进一步实现了 2.71-A h 袋式电池的稳定循环,比能量高达 307 W h kg-1。我们的工作突出了一个基本的化学概念,即调整溶解结构,同时控制电极反应与电解质化学密切相关的金属硫电池的 SRR 和 LMA 稳定性。
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
ACS Energy Letters
ACS Energy Letters Energy-Renewable Energy, Sustainability and the Environment
CiteScore
31.20
自引率
5.00%
发文量
469
审稿时长
1 months
期刊介绍: ACS Energy Letters is a monthly journal that publishes papers reporting new scientific advances in energy research. The journal focuses on topics that are of interest to scientists working in the fundamental and applied sciences. Rapid publication is a central criterion for acceptance, and the journal is known for its quick publication times, with an average of 4-6 weeks from submission to web publication in As Soon As Publishable format. ACS Energy Letters is ranked as the number one journal in the Web of Science Electrochemistry category. It also ranks within the top 10 journals for Physical Chemistry, Energy & Fuels, and Nanoscience & Nanotechnology. The journal offers several types of articles, including Letters, Energy Express, Perspectives, Reviews, Editorials, Viewpoints and Energy Focus. Additionally, authors have the option to submit videos that summarize or support the information presented in a Perspective or Review article, which can be highlighted on the journal's website. ACS Energy Letters is abstracted and indexed in Chemical Abstracts Service/SciFinder, EBSCO-summon, PubMed, Web of Science, Scopus and Portico.
期刊最新文献
Insulin Stabilization Designs for Enhanced Therapeutic Efficacy and Accessibility. Surface Structure and Chemistry of CeO2 Powder Catalysts Determined by Surface-Ligand Infrared Spectroscopy (SLIR). Design, Exploitation, and Rational Improvements of Diazirine-Based Universal Polymer Crosslinkers. Misfit Layered Compounds: Insights into Chemical, Kinetic, and Thermodynamic Stability of Nanophases. Chemical-Driven Amyloid Clearance for Therapeutics and Diagnostics of Alzheimer's Disease.
×
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