Magnesium ion-conducting gel polymer electrolytes dispersed with nanosized magnesium oxide

Experimental investigations are performed on novel magnesium ion-conducting gel polymer electrolyte nanocomposites based on poly(vinylidene fluoride-co-hexafluoropropylene) (PVdF-HFP), dispersed with nanosized magnesium oxide (MgO) particles. The nanocomposite materials are in the form of free-stand...

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Bibliographic Details
Published inJournal of power sources Vol. 190; no. 2; pp. 563 - 572
Main Authors Pandey, G.P., Agrawal, R.C., Hashmi, S.A.
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 15.05.2009
Elsevier
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Summary:Experimental investigations are performed on novel magnesium ion-conducting gel polymer electrolyte nanocomposites based on poly(vinylidene fluoride-co-hexafluoropropylene) (PVdF-HFP), dispersed with nanosized magnesium oxide (MgO) particles. The nanocomposite materials are in the form of free-standing films. Various physical and electrochemical analyses demonstrate promising characteristics of these films, suitable as electrolytes in rechargeable magnesium batteries. The optimized material with 3 wt.% MgO offers a maximum electrical conductivity of ∼8 × 10 −3 S cm −1 at room temperature (∼25 °C) with good thermal and electrochemical stabilities. The ion/filler–polymer interactions and possible conformational changes in host polymer PVdF-HFP due to the liquid electrolyte entrapment and dispersion of nanosized MgO are examined by Fourier transform infrared (FTIR), X-ray diffraction (XRD) and scanning electron microscopic (SEM) methods. The Mg 2+ ion conduction in the gel film is confirmed from the cyclic voltammetry, impedance spectroscopy and transport number measurements. The Mg 2+ ion transport number ( t +) is enhanced substantially and found to have a maximum of ∼0.44 for the addition of 10 wt.% MgO nanoparticles. The enhancement in t + is explained on the basis of the formation of space-charge regions due to the presence of MgO:Mg 2+-like species, that supports Mg 2+ ion motion.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
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ISSN:0378-7753
1873-2755
DOI:10.1016/j.jpowsour.2009.01.057