<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6</volume><submitter>Li D</submitter><pubmed_abstract>Metallic lithium represents a promising anode candidate to be utilized in future high-energy lithium batteries. However, the undesirable dendrite growth and fragile solid-electrolyte interphase (SEI) pose critical challenge for pursuing further practical application. In contrast to traditional approaches of using inert/lithiophilicity coating, here, we demonstrate a reverse strategy of introducing a highly conductive and lithophobic carbon fabric (CF) scaffold on lithium foil to guide a favorable nucleation site of lithium far away from the anode/separator interface. The CF scaffold with high conductivity can couple with inner electric field for achieving a uniform distribution of the lithium-ion flux, while the lithophobic feature offers the condition to guide the preferred deposition of lithium onto the underlying lithium foil, which greatly reduces the risk of dendrite-induced short circuits. Moreover, the SEI immersed in the CF scaffold is well supported by CF fibers and therefore exhibits extremely high stability during charge-discharge cycles. As a result, the lithium/CF anodes show >2,000-h stable cycling at 0.5 mA cm&lt;sup>-2&lt;/sup>. Lithium metal batteries equipped with our lithium/CF anode deliver a high capacity retention of ~99.99% per cycle, i.e., retain ~97.3% capacity after 200 cycles. The unique interface-regulation strategy is versatile for various conductive scaffolds (e.g., ultrathin and ultralight conductive fabrics), exhibiting high superiority for highly safe lithium metal batteries.</pubmed_abstract><journal>Research (Washington, D.C.)</journal><pagination>0267</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10907015</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Constructing Lithium-Free Anode/Separator Interface via 3D Carbon Fabric Scaffold for Ultrasafe Lithium Metal Batteries.</pubmed_title><pmcid>PMC10907015</pmcid><pubmed_authors>Zheng Z</pubmed_authors><pubmed_authors>Li D</pubmed_authors><pubmed_authors>Lai WY</pubmed_authors><pubmed_authors>Yang S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Constructing Lithium-Free Anode/Separator Interface via 3D Carbon Fabric Scaffold for Ultrasafe Lithium Metal Batteries.</name><description>Metallic lithium represents a promising anode candidate to be utilized in future high-energy lithium batteries. However, the undesirable dendrite growth and fragile solid-electrolyte interphase (SEI) pose critical challenge for pursuing further practical application. In contrast to traditional approaches of using inert/lithiophilicity coating, here, we demonstrate a reverse strategy of introducing a highly conductive and lithophobic carbon fabric (CF) scaffold on lithium foil to guide a favorable nucleation site of lithium far away from the anode/separator interface. The CF scaffold with high conductivity can couple with inner electric field for achieving a uniform distribution of the lithium-ion flux, while the lithophobic feature offers the condition to guide the preferred deposition of lithium onto the underlying lithium foil, which greatly reduces the risk of dendrite-induced short circuits. Moreover, the SEI immersed in the CF scaffold is well supported by CF fibers and therefore exhibits extremely high stability during charge-discharge cycles. As a result, the lithium/CF anodes show >2,000-h stable cycling at 0.5 mA cm&lt;sup>-2&lt;/sup>. Lithium metal batteries equipped with our lithium/CF anode deliver a high capacity retention of ~99.99% per cycle, i.e., retain ~97.3% capacity after 200 cycles. The unique interface-regulation strategy is versatile for various conductive scaffolds (e.g., ultrathin and ultralight conductive fabrics), exhibiting high superiority for highly safe lithium metal batteries.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-18T17:17:06.964Z</modification><creation>2025-04-07T04:48:38.484Z</creation></dates><accession>S-EPMC10907015</accession><cross_references><pubmed>38434242</pubmed><doi>10.34133/research.0267</doi></cross_references></HashMap>