{"title":"Recent advances in sulfurized polyacrylonitrile cathodes for lithium–sulfur batteries","authors":"Ting-Hu Tsai and Yu-Sheng Su","doi":"10.1039/D5LF00157A","DOIUrl":null,"url":null,"abstract":"<p >Lithium–sulfur (Li–S) batteries are attractive for next-generation energy storage due to the high theoretical capacity (1675 mA h g<small><sup>−1</sup></small>) and energy density (≈2600 Wh kg<small><sup>−1</sup></small>) of sulfur cathodes. However, traditional sulfur cathodes suffer from severe challenges including the electrical insulation of sulfur, large volume changes upon cycling, and the notorious polysulfide shuttle effect that causes rapid capacity fade. In this regard, sulfurized polyacrylonitrile (SPAN) has emerged as a promising cathode material to overcome these issues. By chemically binding sulfur within a carbon–nitrogen polymer matrix, SPAN completely suppresses polysulfide dissolution and shuttle, enabling highly stable cycling. It is synthesized by simple thermal treatment of polyacrylonitrile with sulfur, yielding a covalently bonded S–C network that is compatible with conventional carbonate electrolytes. This review provides a comprehensive overview of SPAN cathodes, including their structural characteristics and unique solid-state redox mechanism, as well as recent advances in material design and performance optimization. We highlight key studies that elucidate the covalent bonding and lithiation chemistry of SPAN, and we survey state-of-the-art strategies from conductive composites and dopants to electrode engineering, which have elevated its electrochemical performance. Finally, remaining challenges and perspectives for practical Li–S batteries with SPAN cathodes are discussed.</p>","PeriodicalId":101138,"journal":{"name":"RSC Applied Interfaces","volume":" 5","pages":" 1105-1122"},"PeriodicalIF":0.0000,"publicationDate":"2025-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/lf/d5lf00157a?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"RSC Applied Interfaces","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/lf/d5lf00157a","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Lithium–sulfur (Li–S) batteries are attractive for next-generation energy storage due to the high theoretical capacity (1675 mA h g−1) and energy density (≈2600 Wh kg−1) of sulfur cathodes. However, traditional sulfur cathodes suffer from severe challenges including the electrical insulation of sulfur, large volume changes upon cycling, and the notorious polysulfide shuttle effect that causes rapid capacity fade. In this regard, sulfurized polyacrylonitrile (SPAN) has emerged as a promising cathode material to overcome these issues. By chemically binding sulfur within a carbon–nitrogen polymer matrix, SPAN completely suppresses polysulfide dissolution and shuttle, enabling highly stable cycling. It is synthesized by simple thermal treatment of polyacrylonitrile with sulfur, yielding a covalently bonded S–C network that is compatible with conventional carbonate electrolytes. This review provides a comprehensive overview of SPAN cathodes, including their structural characteristics and unique solid-state redox mechanism, as well as recent advances in material design and performance optimization. We highlight key studies that elucidate the covalent bonding and lithiation chemistry of SPAN, and we survey state-of-the-art strategies from conductive composites and dopants to electrode engineering, which have elevated its electrochemical performance. Finally, remaining challenges and perspectives for practical Li–S batteries with SPAN cathodes are discussed.
锂硫电池(Li-S)具有较高的理论容量(1675 mA h g−1)和能量密度(≈2600 Wh kg−1)。然而,传统的硫阴极面临着严峻的挑战,包括硫的电绝缘,循环时的大体积变化,以及臭名昭著的多硫穿梭效应,导致容量迅速衰减。在这方面,硫化聚丙烯腈(SPAN)已成为一种有希望克服这些问题的正极材料。通过在碳氮聚合物基体中化学结合硫,SPAN完全抑制了多硫化物的溶解和穿梭,实现了高度稳定的循环。它是通过用硫对聚丙烯腈进行简单热处理合成的,得到了与常规碳酸盐电解质兼容的共价键S-C网络。本文综述了SPAN阴极的结构特点和独特的固态氧化还原机制,以及材料设计和性能优化方面的最新进展。我们重点介绍了阐明SPAN共价键和锂化化学的关键研究,并概述了从导电复合材料和掺杂剂到电极工程的最新策略,这些策略提高了其电化学性能。最后,讨论了实际使用SPAN阴极的锂离子电池的挑战和前景。