Studies on potassium-ion conducting gel polymer electrolytes containing poly(vinylidene fluoride-hexafluoropropylene) polymer, potassium permanganate salt added with different plasticizers
In this work, a comparative study is presented utilizing a K + conducting gel polymer electrolyte (GPE) system comprising of a poly(vinylidene fluoride-hexafluoropropylene) (PVdF-HFP) polymer matrix combined with potassium permanganate (KMnO 4 ) salt and two different plasticizers as a binary combin...
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Published in: | Ionics Vol. 30; no. 4; pp. 2139 - 2153 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Berlin/Heidelberg
Springer Berlin Heidelberg
01-04-2024
Springer Nature B.V |
Subjects: | |
Online Access: | Get full text |
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Summary: | In this work, a comparative study is presented utilizing a K
+
conducting gel polymer electrolyte (GPE) system comprising of a poly(vinylidene fluoride-hexafluoropropylene) (PVdF-HFP) polymer matrix combined with potassium permanganate (KMnO
4
) salt and two different plasticizers as a binary combination of ethylene carbonate (EC) + propylene carbonate (PC) and tetraethylene glycol dimethyl ether (TEGDME). The electrolyte with TEGDME solvent shows an ionic conductivity (
σ
) of 7.01 × 10
−6
S cm
−1
with hopping of ions as charge transport behavior. The fabricated electrolyte possesses > 98% contribution from the ions, and the electro-chemical stability range is up to 3.2 V. The dielectric analysis shows that the electrolyte with TEGDME solvent possesses a higher value of the dielectric constant, dielectric loss, tangent loss, and dc conductivity, along with a higher free ion number density (
N
) in comparison to the counter-electrolyte specimens with EC:PC solvent. The thermal studies confirm the gel phase of both electrolytes with negligible weight loss till 100 °C. Polymer-salt complex interactions are confirmed using Fourier transform infrared spectroscopy (FTIR), while X-ray diffraction (XRD) analysis is used to study the variations in crystallinity brought about by the polymer and both electrolyte samples. |
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ISSN: | 0947-7047 1862-0760 |
DOI: | 10.1007/s11581-024-05405-8 |