Characteristics of gel electrolytes formed by self-aggregating comb-shaped polyethers with end-functionalised side chains

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Abstract

Gel electrolytes based on comb-shaped polyethers have been prepared and characterised. The comb-shaped polyethers consisted of poly(ethylene oxide) (PEO) or poly(ethylene oxide-co-propylene oxide) (PEOPO) side chains tethered to styrenic backbone polymers. All the polyether side chains were terminated by hydrocarbon (C-16) chain ends. Polymer gel electrolytes were prepared by adding 10-70 wt.% of an electrolyte solution with 1 M lithium bis(trifluoromethylsulfonyl)imide (LiTFSI) salt in gamma-butyrolactone (gamma-BL) or in a mixture of ethylene carbonate and diethyl carbonate (EC/DEC). Thermal analysis by differential scanning calorimetry (DSC) showed endotherms arising from the melting of hydrocarbon phase domains, indicating polymer self-aggregation in the gels by microphase separation of the chain ends. As the concentration of electrolyte solution was increased, the melt temperature of the hydrocarbon phase domains was found to decrease, while the heat of fusion in joules per grain polyether remained essentially constant. The latter finding implied a strong propensity for the hydrocarbon chains to phase separate in the electrolytes. This was further supported by small-angle X-ray scattering measurements which showed a characteristic diffraction distance of approximately 60 A in the gels. The ion conductivity of the electrolytes with 70 wt.% of electrolyte solution added typically reached 10(-2.5) S/cm at 20degreesC. (C) 2004 Elsevier B.V. All rights reserved.

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Subject classification (UKÄ) – MANDATORY

  • Chemical Sciences

Keywords

  • Self-associating graft copolymer, Hydrophobically modified poly(ethylene oxide), Polymer gel electrolyte, Crystallisation, Ionic conductivity
Original languageEnglish
Pages (from-to)417-424
JournalSolid State Ionics
Volume166
Issue number3-4
Publication statusPublished - 2004
Publication categoryResearch
Peer-reviewedYes

Bibliographic note

The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Polymer and Materials Chemistry (LTH) (011001041)