RESUMEN
High-energy density polymer dielectrics play a crucial role in various pulsed energy storage and conversion systems. So far, many strategies have been demonstrated to be able to effectively improve the energy density of polymer dielectrics, but sophisticated fabrication processes are usually needed which result in high cost and poor repeatability. Herein, an easy-operated sputtering and hot-pressing process is developed to significantly enhance the energy density of polymer dielectrics. Surprisingly, for the poly(vinylidene fluoride-hexafluoropropylene) films sputtered with merely 0.0064 vol% gold nanoparticles, the energy density is remarkably improved by 84.3% because of the concurrent enhancements in breakdown strength (by 37.5%) and dielectric permittivity (by 25.5%), which is demonstrated to have originated from the unique Coulomb blockade and micro-capacitor effect of the gold nanoparticles. It is further confirmed that this design strategy is also applicable for commercial biaxially oriented polypropylene and poly(methyl methacrylate). This work offers a novel, easy-operated and universally applicable route to improve the energy density of polymeric dielectrics, which paves the way for their application in modern electronics and power modules.
RESUMEN
Polymers with excellent dielectric properties are strongly desired for pulsed power film capacitors. However, the adverse coupling between the dielectric constant and breakdown strength greatly limits the energy storage capability of polymers. In this work, we report an easily operated method to solve this problem via sputtering the interface of bilayer polymer films with ultralow content of gold nanoparticles. Interestingly, the gold nanoparticles can effectively block the movement of charge carriers because of the Coulomb blocking effect, yielding significantly enhanced breakdown strength. Meanwhile, the gold nanoparticles can act as electrodes to form numerous equivalent microcapacitors, resulting in an obviously enhanced dielectric constant. Impressively, the polymer film with merely 0.01 vol % gold nanoparticles exhibits an obvious dielectric constant and breakdown strength, which are 129 and 131% that of the pristine polymer film, respectively. Consequently, a high energy density which is 176% of that of the pristine polymer film is achieved, and a high efficiency of 79.2% is maintained. Moreover, this process can be well combined with the production process of commercial dielectric polymer films, which is beneficial for mass production. This work offers an easily operated way to improve the dielectric capacitive energy storage properties of polymers, which could also be applicable to other materials, such as ceramics and composites.
