Composition-Function Analyses and Design of Plasticized Solid Polymer Electrolytes for Lithium-ion Batteries

dc.contributor.advisorKofinas, Peteren_US
dc.contributor.authorLudwig, Kyle Brandynen_US
dc.contributor.departmentChemical Engineeringen_US
dc.contributor.publisherDigital Repository at the University of Marylanden_US
dc.contributor.publisherUniversity of Maryland (College Park, Md.)en_US
dc.date.accessioned2023-10-10T05:38:04Z
dc.date.available2023-10-10T05:38:04Z
dc.date.issued2023en_US
dc.description.abstractThis dissertation work examines the electrochemical properties of various solid polymer electrolytes (SPEs) through the lens of composition-function relationships. The analyses presented offer unique design perspectives for improving the performance of SPEs for use in lithium-ion batteries (LIBs). Specifically, three distinct strategies are explored to enhance the lithium ion (Li+) conductivity and reduce the electrode/electrolyte interfacial resistance, two of the major challenges of adopting SPEs as alternatives to common organic liquid electrolytes. The basis for improving ionic conductivity, in all three strategies, is the inclusion of additives in the polymer matrix to plasticize the SPE and improve ionic transport. In one strategy, an ionic liquid (IL) is used as a plasticizer to fabricate free-standing ILSPEs membranes based on a poly(ethylene oxide) (PEO) matrix with an appropriate lithium salt. Optimized ILSPE compositions were able to achieve room temperature ionic conductivity of 0.96 mS/cm, a value suitable for commercial applications, as well as long cycle life in a lithium-metal battery with a capacity of 150—175 mAh/g and >99% coulombic efficiency. In a second strategy, the IL was swapped with water as the plasticizer to fabricate PEO-based aqueous SPEs (ASPEs). The ASPEs exhibited excellent transport properties, with room temperature conductivity values of 0.68—1.75 mS/cm. Molecular dynamics simulations revealed the origin of the exceptional transport properties as the presence of highly interconnected Li+(H2O)n domains. In a final strategy, the concepts of the ILSPE and ASPE were combined through the incorporation of both IL and water into a polymer matrix. For this strategy, the polymer matrix was also changed from PEO to polyacrylonitrile (PAN) to limit the effects of crystallinity and oxidation. These “hybrid aqueous/ionic liquid” SPEs (HAILSPEs) demonstrated the exceptional transport properties of the ASPE system with the improved stability and passivation of the ILSPE system. An analysis of the composition-function relationships correlated the dramatic rise in ionic conductivity to the nearly complete decoupling of ion transport from polymer chain mobility while the unique passivating properties were shown to derive from the choice of ionic liquid, with solid electrolyte interphases comprised of LiF, Li2CO3, Li2S, and Li3N.en_US
dc.identifierhttps://doi.org/10.13016/dspace/1ur1-8b1f
dc.identifier.urihttp://hdl.handle.net/1903/30918
dc.language.isoenen_US
dc.subject.pqcontrolledChemical engineeringen_US
dc.subject.pqcontrolledEnergyen_US
dc.subject.pquncontrolledall-solid-stateen_US
dc.subject.pquncontrolledaqueous electrolyteen_US
dc.subject.pquncontrolledionic liquid electrolyteen_US
dc.subject.pquncontrolledlithium-ionen_US
dc.subject.pquncontrolledsolid polymer electrolyteen_US
dc.titleComposition-Function Analyses and Design of Plasticized Solid Polymer Electrolytes for Lithium-ion Batteriesen_US
dc.typeDissertationen_US

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