Performance studies on composite gel polymer electrolytes for rechargeable magnesium battery application
Effect of micron-sized MgO particles dispersion on poly(vinylidenefluoride-co-hexafluoropropylene) (PVdF–HFP) based magnesium-ion (Mg 2+) conducting gel polymer electrolyte has been studied using various electrical and electrochemical techniques. The composite gel films are free-standing and flexibl...
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Veröffentlicht in: | The Journal of physics and chemistry of solids 2011-12, Vol.72 (12), p.1408-1413 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Effect of micron-sized MgO particles dispersion on poly(vinylidenefluoride-co-hexafluoropropylene) (PVdF–HFP) based magnesium-ion (Mg
2+) conducting gel polymer electrolyte has been studied using various electrical and electrochemical techniques. The composite gel films are free-standing and flexible with enough mechanical strength. The optimized composition with 10
wt% MgO particles offers a maximum electrical conductivity of ∼6×10
−3
S
cm
−1 at room temperature (∼25°C). The Mg
2+ ion conduction in gel film is confirmed from cyclic voltammetry, impedance spectroscopy and transport number measurements. The applicability of the composite gel electrolyte to a rechargeable battery system has been examined by fabricating a prototype cell consisting of Mg (or Mg–MWCNT composite) and V
2O
5 as negative and positive electrodes, respectively. The rechargeability of the cell has been improved, when Mg metal was substituted by Mg–MWCNT composite as negative electrode.
► Studied the effect of micron-sized MgO dispersion on Mg
2+-conducting gel polymer electrolytes. ► Composite gel electrolyte films are fast ion conducting and mechanically stable. ► Dispersion of MgO in gel electrolyte results in enhancement in Mg
2+ ion transport number. ► Applicability of the gel electrolyte is examined in a proto-type rechargeable Mg-battery. ► Rechargeability of the Mg-cell is improved, when Mg metal is replaced by Mg–MWCNT composite anode. |
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ISSN: | 0022-3697 1879-2553 |
DOI: | 10.1016/j.jpcs.2011.08.003 |