## Abstract Poly[(vinylidene fluoride)‐__co__‐hexafluoropropylene]/SiO~2~ polymer electrolytes were prepared by a phase inversion technique using DMAc solvent and water non‐solvent. Cast film electrolytes filled with the same amount of SiO~2~ using DMAc were also made to compare physical and electr
Characteristics of PVdF-HFP/TiO2 Composite Electrolytes Prepared by a Phase Inversion Technique Using Dimethyl Acetamide Solvent and Water Non-Solvent
✍ Scribed by Kwang Man Kim; Jin-Chul Kim; Kwang Sun Ryu
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 259 KB
- Volume
- 291
- Category
- Article
- ISSN
- 1438-7492
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✦ Synopsis
Abstract
Summary: Highly porous poly[(vinylidene fluoride)‐co‐hexafluoropropylene] (PVdF‐HFP)/TiO~2~ membranes were prepared by a phase inversion technique, using dimethyl acetamide (DMAc) as a solvent and water as a non‐solvent. Their physical and electrochemical properties were then characterized in terms of thermal and crystalline behavior, as well as ionic conductivity after absorbing an electrolyte solution of 1 M LiPF~6~ dissolved in an equal weight mixture of ethylene carbonate (EC) and dimethyl carbonate (DMC). For comparison, cast films and their electrolytes were also made by a conventional casting method without using the water non‐solvent. In contrast to the case of using N‐methyl‐2‐pyrrolidone (NMP) as a solvent, the PVdF‐HFP/TiO~2~ composite electrolytes, obtained using DMAc, exhibited superior properties of electrochemical stability and interfacial resistance with a lithium electrode but had lower ionic conductivities. It was also demonstrated that the phase inversion membrane was more effective than the cast film as the polymer electrolyte of a lithium rechargeable battery. As a result, a phase inversion membrane with 50 wt.‐% TiO~2~ was demonstrated to be the optimal choice for application in a lithium rechargeable battery.
Time evolutions of interfacial resistance between polymer electrolyte and lithium electrodes.
magnified imageTime evolutions of interfacial resistance between polymer electrolyte and lithium electrodes.
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