C. Vachon et al., MICROPHASE SEPARATION AND CONDUCTIVITY BEHAVIOR OF POLY(PROPYLENE OXIDE)-LITHIUM SALT ELECTROLYTES, Macromolecules, 28(16), 1995, pp. 5585-5594
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.