LiClO 4 salt concentration effect on the properties of PVC‐modified low molecular weight LENR50‐based solid polymer electrolyte

A work was carried out on a solid polymeric electrolyte system comprising blends of poly (vinyl chloride) and liquid 50% epoxidized natural rubber (LENR50) as a polymer host with LiClO 4 as a salt and prepared by solution casting technique. In this paper, the main study was the effect of LiClO 4 sal...

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Veröffentlicht in:Journal of applied polymer science 2012-05, Vol.124 (3), p.2227-2233
Hauptverfasser: Rahman, M. Y. A., Ahmad, A., Lee, T. K., Farina, Y., Dahlan, H. M.
Format: Artikel
Sprache:eng
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Zusammenfassung:A work was carried out on a solid polymeric electrolyte system comprising blends of poly (vinyl chloride) and liquid 50% epoxidized natural rubber (LENR50) as a polymer host with LiClO 4 as a salt and prepared by solution casting technique. In this paper, the main study was the effect of LiClO 4 salt concentration on the electrolyte properties. The effect of the salt on the electrolyte properties was characterized and analyzed with impedance spectroscopy (EIS), X‐ray diffraction (XRD), differential scanning calorimeter (DSC), and scanning electron microscopy (SEM). The EIS result showed that highest ionic conductivity was obtained at 30 wt % salt with a value of 2.3 × 10 −8 S cm −1 . The XRD results revealed that the LiClO 4 salt was fully complexed within the polymer host as no sharp peaks were observed. However, above 30 wt % of salt, some sharp peaks were observed. This phenomenon was caused by the association of ions. Meanwhile, DSC analysis showed that T g increased as the salt content increased. This implied that LiClO 4 salt had interaction with polymer host by forming coordination bond. The morphologies' studies showed that good homogeneity and compatibility of the electrolyte were achieved. Upon the addition of the salt, formation of micropores occurred. It was noted that micropores which aid in mobility of ions in the electrolyte system has increased the ionic conductivity. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012
ISSN:0021-8995
1097-4628
DOI:10.1002/app.35255