<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang J</submitter><funding>National Key R&amp;D Program of China</funding><funding>China Postdoctoral Science Foundation</funding><funding>National Natural Science Foundation of China</funding><funding>National Key Research and Development Program of China</funding><funding>Natural Science Foundation of Jiangsu Province</funding><pagination>e10894</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12810596</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>38(4)</volume><pubmed_abstract>Low-temperature lithium metal batteries (LT-LMBs) are increasingly desired for higher energy density and longer lifespan. However, due to organic electrolyte solidification, LT-LMBs are impeded by huge barriers resulting from the hindrance of larger solvation shells with strong ion-dipole interactions, leading to depressive Li kinetics and severe dendrite formation. Herein, interfacial catalysis by constructing electron delocalization d-orbital metal oxides toward the ion-dipole interactions is pioneered to accelerate the larger Li(solvents)&lt;sub>x&lt;/sub> &lt;sup>+&lt;/sup> dissociation under the low-temperature environment. Specifically, various kinds of d-orbital metal oxides (M = Ti, V, Fe, Co) with oxygen defect modulation are systematically screened and investigated for breaking the ion-dipol</pubmed_abstract><journal>Advanced materials (Deerfield Beach, Fla.)</journal><pubmed_title>Taming Interfacial Ion-Dipole Interactions With d-Orbital Delocalized Electron Catalysis Expediates Low-Temperature Li Metal Batteries.</pubmed_title><pmcid>PMC12810596</pmcid><funding_grant_id>2023M732561</funding_grant_id><funding_grant_id>21972164</funding_grant_id><funding_grant_id>22572217</funding_grant_id><funding_grant_id>52171191</funding_grant_id><funding_grant_id>2021YFA1201503</funding_grant_id><funding_grant_id>52371198</funding_grant_id><funding_grant_id>BK 20210130</funding_grant_id><funding_grant_id>2023M731084</funding_grant_id><funding_grant_id>22309144</funding_grant_id><funding_grant_id>22279161</funding_grant_id><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Liu M</pubmed_authors><pubmed_authors>Yin S</pubmed_authors><pubmed_authors>Guan Q</pubmed_authors><pubmed_authors>He R</pubmed_authors><pubmed_authors>Jia L</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Cao Z</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>You C</pubmed_authors><pubmed_authors>Miao Y</pubmed_authors><pubmed_authors>Lin H</pubmed_authors><pubmed_authors>Tian N</pubmed_authors><pubmed_authors>Liu F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Taming Interfacial Ion-Dipole Interactions With d-Orbital Delocalized Electron Catalysis Expediates Low-Temperature Li Metal Batteries.</name><description>Low-temperature lithium metal batteries (LT-LMBs) are increasingly desired for higher energy density and longer lifespan. However, due to organic electrolyte solidification, LT-LMBs are impeded by huge barriers resulting from the hindrance of larger solvation shells with strong ion-dipole interactions, leading to depressive Li kinetics and severe dendrite formation. Herein, interfacial catalysis by constructing electron delocalization d-orbital metal oxides toward the ion-dipole interactions is pioneered to accelerate the larger Li(solvents)&lt;sub>x&lt;/sub> &lt;sup>+&lt;/sup> dissociation under the low-temperature environment. Specifically, various kinds of d-orbital metal oxides (M = Ti, V, Fe, Co) with oxygen defect modulation are systematically screened and investigated for breaking the ion-dipol</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-06-06T15:37:47.054Z</modification><creation>2026-06-02T03:08:45.065Z</creation></dates><accession>S-EPMC12810596</accession><cross_references><pubmed>41074733</pubmed><doi>10.1002/adma.202510894</doi></cross_references></HashMap>