Ionic Conductivity in Gelatin-Based Hybrid Solid Electrolytes: The Non-trivial Role of Nanoclay

In this study, the ionic conductivity behavior in hybrid gelatin-based transparent electrolytes including various types of nanoclays with different size, shape and surface properties was characterized. The effects of nanoclay type and nanoclay concentration as well as different experimental conditio...

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Published inJournal of materials science & technology Vol. 30; no. 11; pp. 1096 - 1102
Main Authors Ghadami, Ali, Taheri Qazvini, Nader, Nikfarjam, Nasser
Format Journal Article
LanguageEnglish
Published Elsevier Ltd 01.11.2014
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Summary:In this study, the ionic conductivity behavior in hybrid gelatin-based transparent electrolytes including various types of nanoclays with different size, shape and surface properties was characterized. The effects of nanoclay type and nanoclay concentration as well as different experimental conditions, e.g., pH, temperature and crosslinking were also investigated. In general, the impedance spectroscopy results suggested a non- trivial role for nanoclay. Regardless of the nanoclay type, the ionic conductivity slightly increased first and then decreased by increasing the nanoclay concentration. Furthermore, among sodium montmorillonite (Na+MMT), lithium montmorillonite (Li+MMT), laponite and hydrotalcite, the hybrid electrolytes prepared by Li+MMT showed higher ionic conductivity. The results also showed that the chemical crosslinking along with sample preparation at optimum pH, where the gelatin chains might be efficiently adsorbed on exfoliated, negatively charged clay nanosheets, plays an important role. In comparison with the ionic conductivity of the neat sample at room temperature (~10-7 S cm-1), a ten-fold increase was observed for the crosslinked sample containing 2 wt% of Li^+MMT prepared at optimum pH 3.5. The conductivity behavior as a function of temperature revealed the obedience with the VogeI-Fulcher-Tammann (VFT) model for all samples, suggesting the important role of segmental motions in the ionic conductivity. Finally, a qualitative explanation was presented for the mechanism of the ionic conduction in gelatin-nanoclay hybrid electrolytes.
Bibliography:In this study, the ionic conductivity behavior in hybrid gelatin-based transparent electrolytes including various types of nanoclays with different size, shape and surface properties was characterized. The effects of nanoclay type and nanoclay concentration as well as different experimental conditions, e.g., pH, temperature and crosslinking were also investigated. In general, the impedance spectroscopy results suggested a non- trivial role for nanoclay. Regardless of the nanoclay type, the ionic conductivity slightly increased first and then decreased by increasing the nanoclay concentration. Furthermore, among sodium montmorillonite (Na+MMT), lithium montmorillonite (Li+MMT), laponite and hydrotalcite, the hybrid electrolytes prepared by Li+MMT showed higher ionic conductivity. The results also showed that the chemical crosslinking along with sample preparation at optimum pH, where the gelatin chains might be efficiently adsorbed on exfoliated, negatively charged clay nanosheets, plays an important role. In comparison with the ionic conductivity of the neat sample at room temperature (~10-7 S cm-1), a ten-fold increase was observed for the crosslinked sample containing 2 wt% of Li^+MMT prepared at optimum pH 3.5. The conductivity behavior as a function of temperature revealed the obedience with the VogeI-Fulcher-Tammann (VFT) model for all samples, suggesting the important role of segmental motions in the ionic conductivity. Finally, a qualitative explanation was presented for the mechanism of the ionic conduction in gelatin-nanoclay hybrid electrolytes.
Gelatin; Solid-state electrolytes; Ionic conductivity; Montmorillonitc; Laponite; Impedance spectroscopy
21-1315/TG
Ali Ghadami, Nader Taheri Qazvini, Nasser Nikfarjam(1 Polymer Division, School of Chemistry, College of Science, University of Tehran, Tehran, Iran;2 Biomaterials Research Center (BRC), University of Tehran, Tehran, Iran)
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1005-0302
1941-1162
DOI:10.1016/j.jmst.2014.06.008