{"title":"Polysulfide-mediating properties of nickel phosphide carbon composite nanofibers as free-standing interlayers for lithium–sulfur batteries†","authors":"Ayaulym Belgibayeva, Gulderaiym Turarova, Akmaral Dangaliyeva, Fail Sultanov, Arailym Nurpeissova, Aliya Mukanova and Zhumabay Bakenov","doi":"10.1039/D4RA07285E","DOIUrl":null,"url":null,"abstract":"<p >Issues such as the polysulfide shuttle effect and sulfur loss challenge the development of high-energy-density lithium–sulfur batteries. To address these limitations, a tailored approach is introduced using nickel phosphide carbon composite nanofibers (Ni<small><sub><em>x</em></sub></small>P/C) with controlled surface oxidation layers. These nanofibers feature a hierarchical structure that leverages the benefits of nickel phosphide nanoparticles and a carbonaceous matrix to enable efficient sulfur encapsulation and suppress polysulfide diffusion. Comprehensive characterization and electrochemical testing reveal that Ni<small><sub><em>x</em></sub></small>P/C, when employed as interlayers in a cell with a bio-waste-derived carbon-based sulfur cathode, significantly enhance electrochemical performance by increasing charge–discharge capacities and reducing charge-transfer resistance. Post-mortem analyses further show effective polysulfide trapping and conversion on the cathode side, preventing their shuttle to the anode, which results in a remarkable cycle stability of up to 200 cycles at 2C with a high discharge capacity of about 800 mA h g<small><sup>−1</sup></small>. These findings confirm the potential of Ni<small><sub><em>x</em></sub></small>P/C to improve lithium–sulfur battery technologies and demonstrate their applicability in diverse lithium–sulfur cell configurations.</p>","PeriodicalId":102,"journal":{"name":"RSC Advances","volume":" 49","pages":" 36593-36601"},"PeriodicalIF":3.9000,"publicationDate":"2024-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ra/d4ra07285e?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"RSC Advances","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ra/d4ra07285e","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Issues such as the polysulfide shuttle effect and sulfur loss challenge the development of high-energy-density lithium–sulfur batteries. To address these limitations, a tailored approach is introduced using nickel phosphide carbon composite nanofibers (NixP/C) with controlled surface oxidation layers. These nanofibers feature a hierarchical structure that leverages the benefits of nickel phosphide nanoparticles and a carbonaceous matrix to enable efficient sulfur encapsulation and suppress polysulfide diffusion. Comprehensive characterization and electrochemical testing reveal that NixP/C, when employed as interlayers in a cell with a bio-waste-derived carbon-based sulfur cathode, significantly enhance electrochemical performance by increasing charge–discharge capacities and reducing charge-transfer resistance. Post-mortem analyses further show effective polysulfide trapping and conversion on the cathode side, preventing their shuttle to the anode, which results in a remarkable cycle stability of up to 200 cycles at 2C with a high discharge capacity of about 800 mA h g−1. These findings confirm the potential of NixP/C to improve lithium–sulfur battery technologies and demonstrate their applicability in diverse lithium–sulfur cell configurations.
期刊介绍:
An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.