| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 193674 | Electrochimica Acta | 2007 | 5 Pages |
Polymer electrolytes based on poly(vinyl alcohol) (PVOH) and lithium dihydrogen-phosphate (LiH2PO4) with molar ratio of x = 0.07, 0.10 and 0.14 were prepared in order to investigate the mechanism of ionic motion. Admittance spectroscopy measurements were used to study electrical conductivity relaxation on both anhydrous and hydrated samples in the 5 Hz to 13 MHz frequency range and temperatures ranging from 25 to 150 °C. The conductance, G, shows dispersion above a crossover frequency, fp. This behavior is typical of systems in which correlated ionic motions in the bulk material are responsible for ionic conductivity. For hydrated samples, results reveal that the temperature dependence of the dc-conductivity, σ0 and the characteristic frequency, fp, shows Arrhenius-type behavior with the same energy, Eσ. However, for anhydrous conductivity, a Vogel–Tamman–Fulcher (VTF) behavior is shown for both σ0(T) and fp(T), with the same pseudo activation energy, B and Bσ, respectively, thus indicating that they are correlated with chain mobility.
