Synthesis and electrochemical properties of lithium methacrylate-based self-doped gel polymer electrolytes
In this study, a strategy for synthesizing lithium methacrylate (LiMA)-based self-doped gel polymer electrolytes was described and the electrochemical properties were investigated by impedance spectroscopy and linear sweep voltammetry. LiMA was found to dissolve in ethylene carbonate (EC)/diethyl ca...
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Published in | Electrochimica acta Vol. 54; no. 19; pp. 4540 - 4544 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Kidlington
Elsevier Ltd
30.07.2009
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | In this study, a strategy for synthesizing lithium methacrylate (LiMA)-based self-doped gel polymer electrolytes was described and the electrochemical properties were investigated by impedance spectroscopy and linear sweep voltammetry. LiMA was found to dissolve in ethylene carbonate (EC)/diethyl carbonate (DEC) (3/7, v/v) solvent after complexing with boron trifluoride (BF
3). This was achieved by lowering the ionic interactions between the methacrylic anion and lithium cation. As a result, gel polymer electrolytes consisting of BF
3–LiMA complexes and poly(ethylene glycol) diacrylate were successfully synthesized by radical polymerization in an EC/DEC liquid electrolyte. The FT-IR and AC impedance measurements revealed that the incorporation of BF
3 into the gel polymer electrolytes increases the solubility of LiMA and the ionic conductivity by enhancing the ion disassociations. Despite the self-doped nature of the LiMA salt, an ionic conductivity value of 3.0
×
10
−5
S
cm
−1 was achieved at 25
°C in the gel polymer electrolyte with 49
wt% of polymer content. Furthermore, linear sweep voltammetry measurements showed that the electrochemical stability of the gel polymer electrolyte was around 5.0
V at 25
°C. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0013-4686 1873-3859 |
DOI: | 10.1016/j.electacta.2009.03.050 |