<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Shan J</submitter><funding>National Natural Science Foundation of China</funding><funding>Guangdong Province Universities and Colleges Pearl River Scholar Funded Scheme</funding><funding>Natural Science Foundation of Guangdong Province of China</funding><pagination>e2204192</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9685476</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(33)</volume><pubmed_abstract>Designing dense thick sulfur cathodes to gain high-volumetric/areal-capacity lithium-sulfur batteries (LSBs) in lean electrolytes is extremely desired. Nevertheless, the severe Li&lt;sub>2&lt;/sub> S clogging and unclear mechanism seriously hinder its development. Herein, an integrated strategy is developed to manipulate Li&lt;sub>2&lt;/sub> S redox kinetics of CoP/MXene catalyst via electron-donor Cu doping. Meanwhile a dense S/Cu&lt;sub>0.1&lt;/sub> Co&lt;sub>0.9&lt;/sub> P/MXene cathode (density = 1.95 g cm&lt;sup>-3&lt;/sup> ) is constructed, which presents a large volumetric capacity of 1664 Ah L&lt;sup>-1&lt;/sup> (routine electrolyte) and a high areal capacity of ≈8.3 mAh cm&lt;sup>-2&lt;/sup> (lean electrolyte of 5.0 µL mg&lt;sub>s&lt;/sub> &lt;sup>-1&lt;/sup> ) at 0.1 C. Systematical thermodynamics, kinetics, and theoretical simulati</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Unraveling the Atomic-Level Manipulation Mechanism of Li&lt;sub>2&lt;/sub> S Redox Kinetics via Electron-Donor Doping for Designing High-Volumetric-Energy-Density, Lean-Electrolyte Lithium-Sulfur Batteries.</pubmed_title><pmcid>PMC9685476</pmcid><funding_grant_id>2017</funding_grant_id><funding_grant_id>2021A1515011718</funding_grant_id><funding_grant_id>51972066</funding_grant_id><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Shan J</pubmed_authors><pubmed_authors>Yue L</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Zhou W</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Zhang B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Unraveling the Atomic-Level Manipulation Mechanism of Li&lt;sub>2&lt;/sub> S Redox Kinetics via Electron-Donor Doping for Designing High-Volumetric-Energy-Density, Lean-Electrolyte Lithium-Sulfur Batteries.</name><description>Designing dense thick sulfur cathodes to gain high-volumetric/areal-capacity lithium-sulfur batteries (LSBs) in lean electrolytes is extremely desired. Nevertheless, the severe Li&lt;sub>2&lt;/sub> S clogging and unclear mechanism seriously hinder its development. Herein, an integrated strategy is developed to manipulate Li&lt;sub>2&lt;/sub> S redox kinetics of CoP/MXene catalyst via electron-donor Cu doping. Meanwhile a dense S/Cu&lt;sub>0.1&lt;/sub> Co&lt;sub>0.9&lt;/sub> P/MXene cathode (density = 1.95 g cm&lt;sup>-3&lt;/sup> ) is constructed, which presents a large volumetric capacity of 1664 Ah L&lt;sup>-1&lt;/sup> (routine electrolyte) and a high areal capacity of ≈8.3 mAh cm&lt;sup>-2&lt;/sup> (lean electrolyte of 5.0 µL mg&lt;sub>s&lt;/sub> &lt;sup>-1&lt;/sup> ) at 0.1 C. Systematical thermodynamics, kinetics, and theoretical simulati</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-18T17:07:42.14Z</modification><creation>2025-04-07T04:41:54.899Z</creation></dates><accession>S-EPMC9685476</accession><cross_references><pubmed>36202626</pubmed><doi>10.1002/advs.202204192</doi></cross_references></HashMap>