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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Published in: | Journal of power sources Vol. 187; no. 2; pp. 627 - 634 |
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Main Authors: | , |
Format: | Journal Article |
Language: | English |
Published: |
Amsterdam
Elsevier B.V
15-02-2009
Elsevier |
Subjects: | |
Online Access: | Get full text |
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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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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0378-7753 1873-2755 |
DOI: | 10.1016/j.jpowsour.2008.10.112 |