<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhu C</submitter><funding>Guangzhou Municipal Science and Technology Project</funding><funding>Natural Science Foundation of Guangdong Province</funding><pagination>3435</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9460741</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(17)</volume><pubmed_abstract>Solid-state polymer electrolytes have become promising candidates for high-energy-density lithium metal batteries (LMBs). However, they suffer from low ionic conductivities at room temperature. In this work, two types of composite polymer electrolytes based on a double-network polymer, an ionic liquid (IL) of 1-butyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl) imide (Pyr&lt;sub>14&lt;/sub>TFSI) or 1-ethyl-3-methylimidazolium bis((trifluoromethyl)sulfonyl) imide (EmimTFSI), and bis(trifluoromethane)sulfonamide lithium salt (LiTFSI) were prepared by a facile one-pot method. The two types of CPEs possess good mechanical properties, excellent thermal stability, and high ionic conductivities greater than 10&lt;sup>-4&lt;/sup> S cm&lt;sup>-1&lt;/sup> at 20 °C with 26 wt% IL. The performance diversity of the CPEs was also carefully investigated through a series of electrochemical measurements. Although the CPEs containing EmimTFSI show higher ionic conductivities than those of CPEs with Pyr&lt;sub>14&lt;/sub>TFSI, the latter ones have wider electrochemical stability windows and better resistance to the growth of lithium dendrites. Moreover, CPE with 34 wt% Pyr&lt;sub>14&lt;/sub>TFSI leads to Li/LiFePO&lt;sub>4&lt;/sub> batteries with favorable rate capability and cycling stability and a columbic efficiency of 98.8% at 20 °C, which suggests that CPEs are promising for practical application in solid-state LMBs.</pubmed_abstract><journal>Polymers</journal><pubmed_title>Double-Network Polymer Electrolytes with Ionic Liquids for Lithium Metal Batteries.</pubmed_title><pmcid>PMC9460741</pmcid><funding_grant_id>2020A1515010988</funding_grant_id><funding_grant_id>201904010139</funding_grant_id><pubmed_authors>Jiang Y</pubmed_authors><pubmed_authors>Li G</pubmed_authors><pubmed_authors>Ning Y</pubmed_authors><pubmed_authors>Pan Q</pubmed_authors><pubmed_authors>Zhu C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Double-Network Polymer Electrolytes with Ionic Liquids for Lithium Metal Batteries.</name><description>Solid-state polymer electrolytes have become promising candidates for high-energy-density lithium metal batteries (LMBs). However, they suffer from low ionic conductivities at room temperature. In this work, two types of composite polymer electrolytes based on a double-network polymer, an ionic liquid (IL) of 1-butyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl) imide (Pyr&lt;sub>14&lt;/sub>TFSI) or 1-ethyl-3-methylimidazolium bis((trifluoromethyl)sulfonyl) imide (EmimTFSI), and bis(trifluoromethane)sulfonamide lithium salt (LiTFSI) were prepared by a facile one-pot method. The two types of CPEs possess good mechanical properties, excellent thermal stability, and high ionic conductivities greater than 10&lt;sup>-4&lt;/sup> S cm&lt;sup>-1&lt;/sup> at 20 °C with 26 wt% IL. The performance diversity of the CPEs was also carefully investigated through a series of electrochemical measurements. Although the CPEs containing EmimTFSI show higher ionic conductivities than those of CPEs with Pyr&lt;sub>14&lt;/sub>TFSI, the latter ones have wider electrochemical stability windows and better resistance to the growth of lithium dendrites. Moreover, CPE with 34 wt% Pyr&lt;sub>14&lt;/sub>TFSI leads to Li/LiFePO&lt;sub>4&lt;/sub> batteries with favorable rate capability and cycling stability and a columbic efficiency of 98.8% at 20 °C, which suggests that CPEs are promising for practical application in solid-state LMBs.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2025-04-05T10:25:50.897Z</modification><creation>2025-04-05T10:25:50.897Z</creation></dates><accession>S-EPMC9460741</accession><cross_references><pubmed>36080510</pubmed><doi>10.3390/polym14173435</doi></cross_references></HashMap>