After decades of development, ionic liquid gel polymer electrolytes (ILGPEs) are currently experiencing a renaissance as a promising electrolyte to be used in electrochemical devices. Their inherent tendency towards poor electrochemical properties have limited their applications and commercialization activities. Henceforth, gel polymer electrolyte (GPE) is being introduced to alleviate the abovementioned issues. In this work, the assessment of the ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate [BMIM][BF4] in poly (vinylidene fluoride-hexafluoropropylene) (PVDF-HFP) to form ILGPE was done. The relationship of [BMIM][BF4] towards the dielectric properties at different wt. % ratios and temperature was ascertained. The results indicated that [BMIM]BF4 is able to facilitate fast conduction. Moreover, it was found that [BMIM][BF4] could serve as an effective agent in reducing crystallinity and glass transition temperature of the polymer and thus enhanced the ionic conductivity of the samples. Notwithstanding, the ILGPE sample possessed a high thermal stability up to 300 °C and good electrochemical stability of 4.2 V which are beneficial for operation in electrochemical devices. All in all, the correlation between the ionic liquid chemistry and electrochemical performances could provide a valuable insight to rational selection and design for ILGPE electrolytes.

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This study reported the preparation and characterization of gel polymer electrolyte (GPE) using poly (vinylidine fluoride-co-hexafluoropropylene) (PVdF-HFP), lithium perchlorate (LiClO4) and 1-butyl-3-metilimmidazoliumhexafluorophosphate [PF6]. The GPE were prepared by solution casting technique. [Bmim] [PF6] ionic liquid is used as an additive for the purpose of increasing the ionic conductivity of GPE. Morphological analysis showed that the electrolyte gel polymer sample had a smooth and flat surface with the addition of [Bmim] [PF6] and no phase separation effect was observed. This shows the compatibility between PVdF-HFP and [Bmim] [PF6]. ATR-FTIR analysis showed that C-F bond related peaks experienced peak changes in terms of intensity and peak shifting. This proves the interaction of the imidazolium ion with the fluorine atom through the formation of coordinate bonds. Ionic conductivity analysis showed that PVdF-HFP-[Bmim][PF6] samples reached a maximum room temperature ionic conductivity value of 2.44 × 10-4 S cm-1 at 60 wt.% [Bmim] [PF6]. When 20 wt.% of LiClO4 added to the system, the ionic conductivity increased one magnitude order to 2.20 × 10-3 S cm-1.