Polymer-based dielectric nanocomposites have attracted
great attention
due to the advantages of high-power density and stability. However,
due to the limited breakdown strength (E
b) of the dielectrics, the unsatisfactory energy density becomes the
bottleneck that restricts their applications. Here, newly designed
sandwich-structured nanocomposites are proposed, which includes the
introduction of low-loading 0.4BiFeO3–0.6SrTiO3 (BFSTO) nanofibers into the poly(vinylidene fluoride-co-hexafluoropropylene) (P(VDF-HFP)) matrix as the polarization
layer (B-layer) to offer high permittivity and the selection of poly(methylmethacrylate)
(PMMA)/P(VDF-HFP) all-organic blend film as the insulation layer (P-layer)
to improve E
b of the nanocomposites. The
optimized sandwich-structured PBP nanocomposite exhibits significant
enhancement in E
b (668.6 MV/m), generating
a discharged energy density of 17.2 J/cm3. The dielectric
and Kelvin probe force microscope results corroborate that the outer
P-layer has a low surface charge density, which can markedly impede
the charge injection from the electrode/dielectric interface and thereby
suppress the leakage current inside the nanocomposite. Furthermore,
both the finite element simulations and capacitive series models demonstrate
that the homogenized distribution of electric field in the PBP sandwich-structured
nanocomposite favors the improvement of energy storage performance.
This work not only provides insightful guidance into the in-depth
understanding of the dielectric breakdown mechanism in sandwich-structured
nanocomposites but also offers a novel paradigm for the development
of polymer-based nanocomposites with high E
b and discharged energy density.