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dc.contributor.authorHu, Qichao
dc.contributor.authorCaputo, Antonio
dc.contributor.authorSadoway, Donald Robert
dc.date.accessioned2014-09-16T19:51:30Z
dc.date.available2014-09-16T19:51:30Z
dc.date.issued2013-08
dc.identifier.issn1940-087X
dc.identifier.urihttp://hdl.handle.net/1721.1/89656
dc.description.abstractBattery safety has been a very important research area over the past decade. Commercially available lithium ion batteries employ low flash point (<80 °C), flammable, and volatile organic electrolytes. These organic based electrolyte systems are viable at ambient temperatures, but require a cooling system to ensure that temperatures do not exceed 80 °C. These cooling systems tend to increase battery costs and can malfunction which can lead to battery malfunction and explosions, thus endangering human life. Increases in petroleum prices lead to a huge demand for safe, electric hybrid vehicles that are more economically viable to operate as oil prices continue to rise. Existing organic based electrolytes used in lithium ion batteries are not applicable to high temperature automotive applications. A safer alternative to organic electrolytes is solid polymer electrolytes. This work will highlight the synthesis for a graft copolymer electrolyte (GCE) poly(oxyethylene) methacrylate (POEM) to a block with a lower glass transition temperature (T[subscript g]) poly(oxyethylene) acrylate (POEA). The conduction mechanism has been discussed and it has been demonstrated the relationship between polymer segmental motion and ionic conductivity indeed has a Vogel-Tammann-Fulcher (VTF) dependence. Batteries containing commercially available LP30 organic (LiPF[subscript 6] in ethylene carbonate (EC):dimethyl carbonate (DMC) at a 1:1 ratio) and GCE were cycled at ambient temperature. It was found that at ambient temperature, the batteries containing GCE showed a greater overpotential when compared to LP30 electrolyte. However at temperatures greater than 60 °C, the GCE cell exhibited much lower overpotential due to fast polymer electrolyte conductivity and nearly the full theoretical specific capacity of 170 mAh/g was accessed.en_US
dc.description.sponsorshipWeatherford International, Inc.en_US
dc.language.isoen_US
dc.publisherMyJoVE Corporationen_US
dc.relation.isversionofhttp://dx.doi.org/10.3791/50067en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceMyJoVE Corporationen_US
dc.titleSolid-state Graft Copolymer Electrolytes for Lithium Battery Applicationsen_US
dc.typeArticleen_US
dc.identifier.citationHu, Qichao, Antonio Caputo, and Donald R. Sadoway. “Solid-State Graft Copolymer Electrolytes for Lithium Battery Applications.” JoVE no. 78 (2013). © 2013 Journal of Visualized Experimentsen_US
dc.contributor.departmentMIT Materials Research Laboratoryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineeringen_US
dc.contributor.mitauthorHu, Qichaoen_US
dc.contributor.mitauthorCaputo, Antonioen_US
dc.contributor.mitauthorSadoway, Donald Roberten_US
dc.relation.journalJournal of Visualized Experimentsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsHu, Qichao; Caputo, Antonio; Sadoway, Donald R.en_US
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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