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Concentration dependence of ionic relaxation in lithium doped polymer electrolytes
Uppsala University, Disciplinary Domain of Science and Technology, Technology, Department of Engineering Sciences, Solid State Physics.ORCID iD: 0000-0002-8279-5163
2010 (English)In: Journal of Non-Crystalline Solids, ISSN 0022-3093, E-ISSN 1873-4812, Vol. 356, no 11-17, p. 710-714Article in journal (Refereed) Published
Abstract [en]

A detailed impedance spectroscopy study at ambient temperature was carried out on polymer electrolytes based on low molecular weight poly(ethylene oxide) 400, poly(propylene oxide) 400 and a random copolymer of molecular weight 600, to which were added LiN(CF3SO2)(2) (LiTFSI) salt. The ionic conductivity exhibits a maximum at intermediate salt concentrations and is significantly higher for poly(ethylene oxide) and the copolymer. A dielectric relaxation was found in a frequency region above the one, where the ion conductivity dominates the dielectric response, and below the region of the relaxations of the polymer host. The relaxation strength scales with ion concentration, as appropriate for an ion pair relaxation in systems above the glass transition. The frequency of this relaxation, multiplied by the relaxation strength, has been found to be proportional to the ion conductivity, and the relaxation has therefore been assigned to short-range ionic motion in the polymer. It exhibits characteristics similar to conductivity relaxations in inorganic solid ion conductors, and is considered to be due to the same species that give rise to the ion conductivity.

Place, publisher, year, edition, pages
2010. Vol. 356, no 11-17, p. 710-714
Keyword [en]
Conductivity, Dielectric properties, Relaxation, Electric modulus, Polymers and organics
National Category
Polymer Chemistry Engineering and Technology
Identifiers
URN: urn:nbn:se:uu:diva-137453DOI: 10.1016/j.jnoncrysol.2009.07.039ISI: 000276665500038OAI: oai:DiVA.org:uu-137453DiVA, id: diva2:378510
Available from: 2011-09-21 Created: 2010-12-15 Last updated: 2017-12-11Bibliographically approved

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