DIFFUSION, CONDUCTIVITY AND DSC STUDIES OF A POLYMER GEL ELECTROLYTE COMPOSED OF CROSS-LINKED PEO, GAMMA-BUTYROLACTONE AND LIBF4

Citation
K. Hayamizu et al., DIFFUSION, CONDUCTIVITY AND DSC STUDIES OF A POLYMER GEL ELECTROLYTE COMPOSED OF CROSS-LINKED PEO, GAMMA-BUTYROLACTONE AND LIBF4, Solid state ionics, 107(1-2), 1998, pp. 1-12
Citations number
30
Categorie Soggetti
Physics, Condensed Matter","Chemistry Physical
Journal title
ISSN journal
01672738
Volume
107
Issue
1-2
Year of publication
1998
Pages
1 - 12
Database
ISI
SICI code
0167-2738(1998)107:1-2<1:DCADSO>2.0.ZU;2-X
Abstract
The gel electrolyte system composed of gamma-butyrolactone (GBL), LiBF 4, and cross-linked acrylated polyethylene oxide (PEG) with a molecula r weight of 4000 (PEO4) was studied using the pulsed field gradient (P FG) NMR method to measure the diffusion coefficients. The NMR spin-lat tice relaxation times, ionic conductivities and thermal behaviour were also measured. Seven reference samples were also prepared: pure GEL ( sample A), 0.5, 1 and 1.5 M LiBF4 in GEL (i.e., solution electrolyte; samples B-D), 20 wt % PEO4 in GEL (sample E), 1 M LiBF4 plus 20 wt % P EO4 in GEL (sample F) and a gel without the salt (sample G), in additi on to three gel electrolyte samples containing 0.5, 1, and 1.5 M conce ntrations of LIBF4 in GEL with 20 wt % cross-linked PEO4 (samples H-J) . Importantly, using H-1, Li-7, and F-19 PFG NMR the diffusion coeffic ients of all the species present were able to be measured. The diffusi on coefficients were found to be sensitive to the salt concentration a nd the cross-linking of the polymer. The Li and BF4 ions are solvated with GEL even in the gel state. The deviation of the measured conducti vities from the values calculated using the Nernst-Einstein equation r eflects the effects of ion association. It was observed that at least, at low salt concentrations, the polymer aids in the dissociation of t he salt. By considering all of the experimental data obtained, we show that in the gel system the BF4 ions exist predominantly in the solven t while the motion of the Li ions, although solvated in GEL, is strong ly associated with the polymer. From the combination of the conductivi ty and diffusion measurements we were able to obtain values for the di ssociation constants for the salt dissolved in the GEL and in the gel samples.