MICROPHASE SEPARATION AND CONDUCTIVITY BEHAVIOR OF POLY(PROPYLENE OXIDE)-LITHIUM SALT ELECTROLYTES

Citation
C. Vachon et al., MICROPHASE SEPARATION AND CONDUCTIVITY BEHAVIOR OF POLY(PROPYLENE OXIDE)-LITHIUM SALT ELECTROLYTES, Macromolecules, 28(16), 1995, pp. 5585-5594
Citations number
23
Categorie Soggetti
Polymer Sciences
Journal title
ISSN journal
00249297
Volume
28
Issue
16
Year of publication
1995
Pages
5585 - 5594
Database
ISI
SICI code
0024-9297(1995)28:16<5585:MSACBO>2.0.ZU;2-O
Abstract
A DSC study performed on poly(propylene oxide) (PPO) electrolytes cont aining various lithium salts (LiBr, LiClO4, LiCF3SO3, and LiN(CF3SO2)( 2)) shows that microphase separation is a general feature of PPO-LiX s ystems. Below a certain salt content, which corresponds to O/Li = 9 (O = ether oxygen) for LiBr, to O/Li = 10 for LiClO4 and LiCF3SO3, and t o O/Li = 16 for LiN(CF3SO2)(2), two glass transition (T-g) features ar e recorded on optically clear mixtures of these systems. A comparison made with poly(ethylene oxide) (PEG) electrolytes shows that this phas e complication has a strong effect on the conduction process. For the PPO-LiBr and PPO-LiClO4 systems, which involve a large difference betw een the compositions of their low-T-g and high-T-g microphases, a perc olation threshold occurs over the range where related PEO-LiX electrol ytes exhibit their conductivity maximum. A similar but less pronounced effect is systematically observed for the other PPO-LiX systems and f or non-PPO systems that exhibit an initial accelerated rise in their T -g-composition relationships. The PEO-LiX systems are free from these anomalies.