Communication: Enhanced cation transport in polymer electrolytes, with cons
equent improved performance in batteries and other electrochemical applicat
ions, is reported. In general, ionic transport in polymer electrolytes is c
losely coupled to segmental motion of the backbone, leading to severely res
tricted cation mobility as the glass transition temperature T-g is approach
ed. In the new side-group liquid-crystalline polymer electrolyte system des
cribed here, the ionic conductivity is shown to be insensitive to T-g, with
sub-T-g conductivities of similar to 10(-5) Scm(-1). An explanation for th
is behavior is proposed.