Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/106660
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dc.contributor.authorRajendran, S.en
dc.contributor.authorKesavan, K.en
dc.contributor.authorNithya, R.en
dc.contributor.authorUlaganathan, Manien
dc.date.accessioned2013-06-28T07:37:54Zen
dc.date.accessioned2019-12-06T22:15:47Z-
dc.date.available2013-06-28T07:37:54Zen
dc.date.available2019-12-06T22:15:47Z-
dc.date.copyright2011en
dc.date.issued2011en
dc.identifier.citationRajendran, S., Kesavan, K., Nithya, R., & Ulaganathan, M. (2012). Transport, structural and thermal studies on nanocomposite polymer blend electrolytes for Li-ion battery applications. Current Applied Physics, 12(3), 789-793.en
dc.identifier.issn1567-1739en
dc.identifier.urihttps://hdl.handle.net/10356/106660-
dc.description.abstractNanocomposite polymer electrolytes (NCPEs) composed of poly(vinylidenefluoride-co-hexafluoropropylene) (PVdF-co-HFP) as a host polymer, Poly(vinyl acetate) (PVAc) as an additive, Ethylene Carbonate (EC) as a plasticizer, Lithium Perchlorate as dopant salt and Barium Titanate (BaTiO3) as a filler were prepared for various concentrations of BaTiO3 using solvent casting technique. Thermal stability of the sample having maximum ionic conductivity was found using TG/DTA analysis. Nano composite polymer electrolytes were subjected to ac impedance analysis spectra for acquiring the ionic conductivity values at different temperature. Surface structure of the sample was analysed using scanning electron microscope and the complexations of samples were analysed using X-ray diffraction analysis. It was noted that the polymer electrolyte contains 8 wt. % of BaTiO3 showed maximum ionic conductivity than the other ratios of BaTiO3.en
dc.language.isoenen
dc.relation.ispartofseriesCurrent applied physicsen
dc.rights© 2011 Elsevier B.V.en
dc.titleTransport, structural and thermal studies on nanocomposite polymer blend electrolytes for Li-ion battery applicationsen
dc.typeJournal Articleen
dc.contributor.researchEnergy Research Institute @NTUen
dc.identifier.doi10.1016/j.cap.2011.11.006en
item.fulltextNo Fulltext-
item.grantfulltextnone-
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