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°C), where an isothermal entropy change of more than 55 joules per kilogram per kelvin degree and adiabatic temperature change of more than 12°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).

Polymer film capacitors are critical components in many high-power electrical systems. Because of the low energy density of conventional polymer dielectrics, these capacitors currently occupy significant volume in the entire electrical system. This article reviews recent progress made in the development of polymer dielectrics with high energy storage density, which can potentially lead to significant weight and volume reduction in polymer film capacitors. The increase in energy density is achieved through two approaches, namely (a) the development of novel polymers with high electric polarization and optimized dielectric responses and (b) the development of nanocomposites containing polymer matrixes with high breakdown strength and inorganic nanofillers with high polarization. Promising progress has been made through both strategies, resulting in a maximum energy density of >30 J/cm³, which is at least 5 times higher than those of conventional polymer dielectrics. The state-of-the-art manufacturing method for low-cost, high-throughput production of polymer films is also reviewed.