Applying an electrical field to a polar polymer may induce a large change in the dipolar ordering, and if the associated entropy changes are large, they can be explored in cooling applications. With the use of the Maxwell relation between the pyroelectric coefficient and the electrocaloric effect (ECE), it was determined that a large ECE can be realized in the ferroelectric poly(vinylidene fluoride-trifluoroethylene) [P(VDF-TrFE)] copolymer at temperatures above the ferroelectric-paraelectric transition (above 70 degrees C), where an isothermal entropy change of more than 55 joules per kilogram per kelvin degree and adiabatic temperature change of more than 12 degrees C were observed. We further showed that a similar level of ECE near room temperature can be achieved by working with the relaxor ferroelectric polymer of P(VDF-TrFE-chlorofluoroethylene).

A phenomenological thermodynamic theory of PbTiO3 was developed using a modified Devonshire form of the elastic Gibbs free energy. The spontaneous strain as a function of temperature was determined from pure sol-gel derived PbTiO3 powder and used with selected data from the literature to determine the coefficients of the energy function. The theoretical prediction of the phase stability, spontaneous polarization and strains, and dielectric and piezoelectric properties agree well with experimental data. This theory provides a way of predicting the intrinsic single domain dielectric and piezoelectric properties of PbTiO3, which have not been completely determined from experimental measurements.

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