Construction of ternary core-shell Fe3O4@BaTiO3/PVDF nanocomposites with enhanced permittivity and breakdown strength for energy storage

Introducing conductive nanoparticles into ferroelectric polymers gives rise to significant enhancement of permittivity (epsilon), making these composites practically promising for energy storage devices. However, the breakdown strength (E-B) of such composites is reduced with few exceptions, which limits high-performance applications. Here we study the energy storage behavior of well-designed Fe3O4@BaTiO3 core-shell nanoparticle/poly(vinylidene fluoride) (PVDF) nanocomposites in which conductive Fe3O4 nanoparticles (NPs) are coated by ferroelectric BaTiO3 (BT), together with the PVDF matrix, forming the ternary nanocomposite films with high energy storage performance. Notably, the permittivity is enhanced by increasing the volume fraction of the Fe3O4@BT NPs, reaching 38 with 2 vol% Fe3O4@BT NPs and remaining low dielectric loss (similar to 0.066). In particular, the nanocomposites exhibit moderate breakdown strength (similar to 430 kV/mm), which is attributed to the voltage dispersion layer (the BaTiO3 shell) between the polymer matrix and Fe3O4 NPs. The finite element simulation substantiates the experimental results and further confirms the positive correlation of the breakdown strength and the permittivity of the voltage dispersion layer. With the synergistic effect of both breakdown strength and electric displacement, a remarkable energy density (16 J/cc, at 430 kV/mm) is obtained.

Automated summary

Introducing conductive nanoparticles into ferroelectric polymers significantly enhances the permittivity of composites, making them promising for energy storage devices. However, the breakdown strength of such composites is often reduced, posing limitations for high-performance applications. By designing Fe3O4@BaTiO3 core-shell nanoparticle/PVDF nanocomposites, moderate breakdown strength and high energy storage performance are achieved through a voltage dispersion layer mechanism.