J. Li et Im. Khan, HIGHLY CONDUCTIVE SOLID POLYMER ELECTROLYTES PREPARED BY BLENDING HIGH-MOLECULAR-WEIGHT POLY(ETHYLENE OXIDE), POLY(2-VINYLPYRIDINE OR 4-VINYLPYRIDINE), AND LITHIUM PERCHLORATE, Macromolecules, 26(17), 1993, pp. 4544-4550
Highly ionic conductive solid polymer electrolytes have been prepared
by blending poly(ethylene oxide) (MW 600 000) and poly(2-vinylpyridine
) (MW 200 000) or poly(4-vinylpyridine) (MW 50 000) and LiClO4. All bl
ends were prepared by the solution blending process. Several different
blend compositions have been studied and optimum compositions require
d for preparing solid polymer electrolytes have been determined. The p
oly(ethyleneoxide) (85% by weight)/poly(2-vinylpyridine) (15% by weigh
t)/LiClO4 blend at an ethylene oxide/Li+ mole ratio of 10 exhibits an
ionic conductivity value of 1.0 x 10(-5) S cm-1 at 25-degrees-C and is
an elastomeric material with dimensional stability. Furthermore, this
blend exhibits ionic conductivities >3.0 x 10(-6) S cm-1 at 25-degree
s-C over a wide salt concentration range. Several other blends prepare
d are also elastomeric materials with ionic conductivities approximate
ly 5.0 x 10(-6) S cm-1, e.g. poly(ethylene oxide) (85% by weight)/poly
(2-vinylpyridine) (15% by weight)/LiClO4 at an ethylene oxide to Li+ m
ole ratio of 6 exhibits a value of 7.0 x 10(-6) S cm-1 at 30-degrees-C
. Studies indicate that the LiClO4 salt compatibilizes the poly(ethyle
ne oxide) and the poly(2-vinylpyridine) by the simultaneous interactio
n of the Li+ with the oxygens of the PEO and nitrogen of the pyridyl u
nits. Scanning electron microscopy (SEM) on the internal structure of
the blends shows the presence of a two phase microstructure, most like
ly, stabilized by the emulsifying effect of LiClO4.