D. Bamford et al., The local free volume, glass transition, and ionic conductivity in a polymer electrolyte: A positron lifetime study, J CHEM PHYS, 115(15), 2001, pp. 7260-7270
The size of free-volume holes in neat poly[(ethylene glycol)(23)dimethacryl
ate] [poly((EG)(23)DMA)] and in the same polymer doped with 0.6 mol/kg LiCF
3SO3 have been studied as a function of temperature in the range between 10
0 and 370 K using positron annihilation lifetime spectroscopy. The results
are compared with differential scanning calorimetry and ionic conductivity
measurements. In both systems, the hole volume nu (h) shows a typical glass
-transition behavior, i.e., a small linear increase with temperature below
the glass transition temperature T-g and a steeper increase above T-g. From
these measurements T-g was estimated to be 233 K (neat polymer) and 240 K
(polymer with salt) and the coefficients of the thermal expansion of the ho
le volume were determined. The fractional free volume (f=0.080) and the num
ber density of holes (N-h=0.6 nm(-3)) were also estimated. Below T-g the av
erage hole volume of the polymer electrolyte is larger than in the neat pol
ymer. This is consistent with the bulky character of the CF3SO3- anion. Abo
ve T-g the salt-doped system shows the lower hole volume of the two systems
, probably caused by a reduced segmental mobility as a consequence of the i
nteractions of the Li+ ions with the ethylene oxide units of the polymer. B
ased on the free-volume theory of Cohen-Turnbull the ionic conductivity sig
ma is correlated with the mean hole volume nu (h). A linear relation betwee
n log(sigmaT (0.5)) and 1/nu (h) was observed to be valid for variations of
the conductivity over several orders of magnitudes. From these plots criti
cal hole sizes of gamma nu*=0.65 nm(3) (neat polymer) and 0.87 nm(3) (polym
er-salt system) were estimated. The parameters B and T-0 of the Vogel-Tamma
n-Fulcher equation were also determined, as well as the apparent activation
volume DeltaV(app) by pressure-dependent conductivity measurements. The ca
tionic transference number in the polymer-salt system was determined by pul
sed field gradient-nuclear magnetic resonance to be t(+)approximate to0.3.
(C) 2001 American Institute of Physics.