Ruyi Bi, Jilu Zhao, Mei Yang, Jiangyan Wang, Ranbo Yu and Dan Wang
{"title":"Multifunctional separator modified with catalytic multishelled structural CoS2 enables a stable lithium–sulfur battery†","authors":"Ruyi Bi, Jilu Zhao, Mei Yang, Jiangyan Wang, Ranbo Yu and Dan Wang","doi":"10.1039/D4QI02340D","DOIUrl":null,"url":null,"abstract":"<p >Lithium–sulfur batteries have been considered as promising next-generation energy storage devices due to their ultrahigh theoretical energy density and natural abundance of sulfur. However, the shuttle effect and sluggish redox kinetics of polysulfides hinder their commercial applications. Herein, by combining smart material design and structure engineering, a CoS<small><sub>2</sub></small> hollow multishelled structure (HoMS) has been developed to modify the separator and establish a “vice electrode”, which effectively hinders the shuttle effect and catalyzes redox reactions. CoS<small><sub>2</sub></small> HoMS can not only obstruct polysulfides through multiple shell barriers but also provide a large available polar surface to effectively capture polysulfides. Additionally, CoS<small><sub>2</sub></small> HoMS, with good conductivity, could greatly accelerate the redox conversion of polysulfides and enhance the decomposition of Li<small><sub>2</sub></small>S. Moreover, CoS<small><sub>2</sub></small> HoMS can buffer the large volume change of sulfur during cycling, ensuring good contact and stability of the electrodes. As a result, the lithium–sulfur battery with the CoS<small><sub>2</sub></small> HoMS-modified separator exhibited a high discharge capacity of 873.1 mA h g<small><sup>−1</sup></small> at a high rate of 1 C, with only 0.054% capacity decay per cycle during 350 cycles.</p>","PeriodicalId":79,"journal":{"name":"Inorganic Chemistry Frontiers","volume":" 24","pages":" 8837-8846"},"PeriodicalIF":6.4000,"publicationDate":"2024-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/qi/d4qi02340d?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/qi/d4qi02340d","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
Lithium–sulfur batteries have been considered as promising next-generation energy storage devices due to their ultrahigh theoretical energy density and natural abundance of sulfur. However, the shuttle effect and sluggish redox kinetics of polysulfides hinder their commercial applications. Herein, by combining smart material design and structure engineering, a CoS2 hollow multishelled structure (HoMS) has been developed to modify the separator and establish a “vice electrode”, which effectively hinders the shuttle effect and catalyzes redox reactions. CoS2 HoMS can not only obstruct polysulfides through multiple shell barriers but also provide a large available polar surface to effectively capture polysulfides. Additionally, CoS2 HoMS, with good conductivity, could greatly accelerate the redox conversion of polysulfides and enhance the decomposition of Li2S. Moreover, CoS2 HoMS can buffer the large volume change of sulfur during cycling, ensuring good contact and stability of the electrodes. As a result, the lithium–sulfur battery with the CoS2 HoMS-modified separator exhibited a high discharge capacity of 873.1 mA h g−1 at a high rate of 1 C, with only 0.054% capacity decay per cycle during 350 cycles.