Physical and charge discharge behavior of facile PVDF-HFP nanocomposite microporous polymer electrolyte for lithium ion polymer batteries
Synthesized wurtzite ZnO nanostructures are incorporated on the poly (vinylidenefluoride-co-hexafluoropropylene) (PVdF-HFP) matrix, which improves the thermal as well as porosity nature of as obtained thin film nanocomposite microporous polymer membrane (nanoCMPM). The membrane shows a favorable eff...
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Veröffentlicht in: | Journal of materials science. Materials in electronics 2022-04, Vol.33 (11), p.8594-8606 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Synthesized wurtzite ZnO nanostructures are incorporated on the poly (vinylidenefluoride-co-hexafluoropropylene) (PVdF-HFP) matrix, which improves the thermal as well as porosity nature of as obtained thin film nanocomposite microporous polymer membrane (nanoCMPM). The membrane shows a favorable effect on the crystallinity (
X
c
) of 26.83% and melting temperature (
T
m
) of 142.9 °C that improves the conductivity of polymer electrolytes. Its characteristics were examined by thermal studies. The optimized polymer membrane was found to have a high degree of porosity (76%) and excellent film strength. The membranes were prepared as a polymer electrolytes in soaking lithium percholoride (LiClO
4
) salt solution and ethylene carbonate (EC) as well as dimethylene carbonate (DMC) in 1: 1 (
v/v
) ratio as plasticizer to form gel type nanocomposite microporous polymer electrolytes (nanoCMPE). It shows the ionic conductivity in the order of 10
−3
S cm
−1
at 298 K for all optimized polymer electrolytes with different lithium salt electrolyte concentrations. The polymer membrane electrolyte has good compatibility and fabricates [LiCoO
2
/PVDF-HFP-ZnO-LiClO
4
/mesocarbon microbeads (MCMB)] as coin type cell. The charge–discharge characteristics as well as cell performance were investigated at 0.5 C rate. The polymer electrolyte is a better candidate to perform in lithium ion polymer batteries. |
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ISSN: | 0957-4522 1573-482X |
DOI: | 10.1007/s10854-021-06622-x |