<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Belgibayeva A</submitter><funding>Ministry of Education and Science of the Republic of Kazakhstan</funding><pagination>36593-36601</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11565693</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(49)</volume><pubmed_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 (Ni &lt;sub>&lt;i>x&lt;/i>&lt;/sub> 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 &lt;sub>&lt;i>x&lt;/i>&lt;/sub> 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&lt;sup>-1&lt;/sup>. These findings confirm the potential of Ni &lt;sub>&lt;i>x&lt;/i>&lt;/sub> P/C to improve lithium-sulfur battery technologies and demonstrate their applicability in diverse lithium-sulfur cell configurations.</pubmed_abstract><journal>RSC advances</journal><pubmed_title>Polysulfide-mediating properties of nickel phosphide carbon composite nanofibers as free-standing interlayers for lithium-sulfur batteries.</pubmed_title><pmcid>PMC11565693</pmcid><funding_grant_id>BR21882402</funding_grant_id><funding_grant_id>AP13068219</funding_grant_id><pubmed_authors>Turarova G</pubmed_authors><pubmed_authors>Sultanov F</pubmed_authors><pubmed_authors>Belgibayeva A</pubmed_authors><pubmed_authors>Dangaliyeva A</pubmed_authors><pubmed_authors>Mukanova A</pubmed_authors><pubmed_authors>Bakenov Z</pubmed_authors><pubmed_authors>Nurpeissova A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Polysulfide-mediating properties of nickel phosphide carbon composite nanofibers as free-standing interlayers for lithium-sulfur batteries.</name><description>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 &lt;sub>&lt;i>x&lt;/i>&lt;/sub> 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 &lt;sub>&lt;i>x&lt;/i>&lt;/sub> 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&lt;sup>-1&lt;/sup>. These findings confirm the potential of Ni &lt;sub>&lt;i>x&lt;/i>&lt;/sub> P/C to improve lithium-sulfur battery technologies and demonstrate their applicability in diverse lithium-sulfur cell configurations.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2025-04-04T01:21:34.479Z</modification><creation>2025-04-04T01:21:34.479Z</creation></dates><accession>S-EPMC11565693</accession><cross_references><pubmed>39553272</pubmed><doi>10.1039/d4ra07285e</doi></cross_references></HashMap>