Dr. Mengxue He, Lujun Zhu, Dr. Yatao Liu, Yongfeng Jia, Yizhou Hao, Dr. Guo Ye, Xufeng Hong, Dr. Zhitong Xiao, Dr. Yue Ma, Prof. Jianhao Chen, Muhammad Burhan Shafqat, Prof. Quanquan Pang
{"title":"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","authors":"Dr. Mengxue He, Lujun Zhu, Dr. Yatao Liu, Yongfeng Jia, Yizhou Hao, Dr. Guo Ye, Xufeng Hong, Dr. Zhitong Xiao, Dr. Yue Ma, Prof. Jianhao Chen, Muhammad Burhan Shafqat, Prof. Quanquan Pang","doi":"10.1002/anie.202415053","DOIUrl":null,"url":null,"abstract":"<p>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 [S<sub>3</sub>]⋅<sup>−</sup> radical, favoring a rapid radical-mediated solution-based SRR. The cell with the proposed electrolyte showing a high capacity of 864 mAh g<sub>sulfur</sub><sup>−1</sup> under high sulfur loading of 5.5 mg<sub>sulfur</sub> cm<sup>−2</sup> and low E/S ratio of 4 μL mg<sub>sulfur</sub><sup>−1</sup>. The strategy further enables steady cycling of a 2.71-A h pouch cell with a high specific energy of 307 W h kg<sup>−1</sup>. 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.</p>","PeriodicalId":125,"journal":{"name":"Angewandte Chemie International Edition","volume":"64 3","pages":""},"PeriodicalIF":16.1000,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Highly Solvating Electrolytes with Core-Shell Solvation Structure for Lean-Electrolyte Lithium-Sulfur Batteries\",\"authors\":\"Dr. Mengxue He, Lujun Zhu, Dr. Yatao Liu, Yongfeng Jia, Yizhou Hao, Dr. Guo Ye, Xufeng Hong, Dr. Zhitong Xiao, Dr. Yue Ma, Prof. Jianhao Chen, Muhammad Burhan Shafqat, Prof. Quanquan Pang\",\"doi\":\"10.1002/anie.202415053\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>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 [S<sub>3</sub>]⋅<sup>−</sup> radical, favoring a rapid radical-mediated solution-based SRR. The cell with the proposed electrolyte showing a high capacity of 864 mAh g<sub>sulfur</sub><sup>−1</sup> under high sulfur loading of 5.5 mg<sub>sulfur</sub> cm<sup>−2</sup> and low E/S ratio of 4 μL mg<sub>sulfur</sub><sup>−1</sup>. The strategy further enables steady cycling of a 2.71-A h pouch cell with a high specific energy of 307 W h kg<sup>−1</sup>. 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.</p>\",\"PeriodicalId\":125,\"journal\":{\"name\":\"Angewandte Chemie International Edition\",\"volume\":\"64 3\",\"pages\":\"\"},\"PeriodicalIF\":16.1000,\"publicationDate\":\"2024-11-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Angewandte Chemie International Edition\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/anie.202415053\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie International Edition","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/anie.202415053","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
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。
Highly Solvating Electrolytes with Core-Shell Solvation Structure for Lean-Electrolyte Lithium-Sulfur Batteries
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 mAh 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.
期刊介绍:
Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.