Experimental investigations of an ionic-liquid-based, magnesium ion conducting, polymer gel electrolyte

Studies on a novel magnesium ion conducting gel polymer electrolyte based on a room temperature ionic liquid (RTIL) is reported. It comprises a Mg-salt, Mg(CF 3SO 3) 2 [or magnesium triflate, Mg(Tf) 2] solution in an ionic liquid, 1-ethyl-3-methylimidazolium trifluoro-methanesulfonate (EMITf), immob...

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Bibliographic Details
Published in:Journal of power sources Vol. 187; no. 2; pp. 627 - 634
Main Authors: Pandey, G.P., Hashmi, S.A.
Format: Journal Article
Language:English
Published: Amsterdam Elsevier B.V 15-02-2009
Elsevier
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Summary:Studies on a novel magnesium ion conducting gel polymer electrolyte based on a room temperature ionic liquid (RTIL) is reported. It comprises a Mg-salt, Mg(CF 3SO 3) 2 [or magnesium triflate, Mg(Tf) 2] solution in an ionic liquid, 1-ethyl-3-methylimidazolium trifluoro-methanesulfonate (EMITf), immobilized with poly(vinylidene fluoride-hexafluoropropylene) (PVdF-HFP), which is a freestanding, semitransparent and flexible film with excellent mechanical strength. Physical and electrochemical analyses demonstrate promising characteristics of these films, suitable as electrolytes in rechargeable magnesium batteries. The material offers a maximum electrical conductivity of ∼4.8 × 10 −3 S cm −1 at room temperature (20 °C) with excellent thermal and electrochemical stabilities. Possible conformational changes in the polymer host PVdF-HFP due to ionic liquid solution entrapment and ion–polymer interaction are investigated by Fourier transform infra-red (FTIR), X-ray diffraction (XRD) and scanning electron microscopic (SEM) methods. The Mg 2+ ion transport in the gel film is confirmed from cyclic voltammetry, impedance and transport number measurements. The Mg 2+ ion transport number ( t +) is ∼0.26, which indicates a substantial contribution of triflate anion transport along with ionic conduction due to the component ions of the ionic liquid.
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ISSN:0378-7753
1873-2755
DOI:10.1016/j.jpowsour.2008.10.112