Diffusion of solvent/salt and segmental relaxation in polymer gel electrolytes

Citation
C. Svanberg et al., Diffusion of solvent/salt and segmental relaxation in polymer gel electrolytes, ELECTR ACT, 46(10-11), 2001, pp. 1447-1451
Citations number
12
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
ELECTROCHIMICA ACTA
ISSN journal
00134686 → ACNP
Volume
46
Issue
10-11
Year of publication
2001
Pages
1447 - 1451
Database
ISI
SICI code
0013-4686(20010315)46:10-11<1447:DOSASR>2.0.ZU;2-K
Abstract
Dynamic light scattering and broad band impedance spectroscopy have been pe rformed on polymer gel electrolytes consisting of a mixture of propylene ca rbonate/lithium perchlorate (PC/LiClO4) stabilised with a polymer matrix, p oly(methyl methacrylate) (PMMA), The salt concentration and temperature dep endences of the conductivity are compared to the dynamical behaviour of the system. Complex relaxation dynamics is observed in the dynamic light scatt ering experiments with multiple relaxation processes with different tempera ture and wave vector dependencies. In focus here is a fast exponential deca y attributed to diffusion of low molecular compounds and a slower and very broad relaxation process attributed to the segmental motion of the polymer backbone. The relation between the relaxation processes and the ionic condu ctivity is investigated, with special emphasis on the relation to the fast diffusive process. We show that the slowing down of this diffusion process is a more important limiting factor for ionic conductivity than the possibl e creation of ion pairs at higher salt-concentrations. The physical picture that emerges from the results is that the conductivity mechanism is a diff usion of ions moving together with the solvent molecules, both of which are essentially decoupled from the segmental motion of the polymer backbone. ( C) 2001 Elsevier Science Ltd. All rights reserved.