Polymer–ceramic piezoelectric composites are widely investigated to combine the high piezoelectric performance of ferroelectric ceramics with the flexibility and processability of electroactive polymers. However, achieving enhanced dielectric properties while preserving the intrinsic piezoelectric response of the polymer matrix remains challenging, particularly due to dielectric mismatch between the constituent phases and interfacial effects. In this work, barium titanate (BaTiO3) loaded poly(vinylidene fluoride-trifluoroethylene) (PVDF-TrFE) nanocomposites were fabricated by solvent casting using polyvinylpyrrolidone (PVP) and polysorbate 80 (PS80) as dispersing agents, aiming to obtain polarizable materials capable of retaining high piezoelectric strain coefficient (d33) values and potentially exploiting the opposite polarity of matrix and filler through tailored poling strategies. Morphological, crystallographic, structural, thermal, thermomechanical, dielectric, and piezoelectric characterizations were performed by SEM/EDXS, XRD, FTIR, DSC, TGA, DMTA, dielectric spectroscopy, and d33 measurements. Both dispersants improved filler dispersion and film densification, increasing the crystalline fraction of the matrix, without altering the relative fraction of β-phase (up to 93%). PVP enabled moderate and stable permittivity enhancement with weak frequency dependence, whereas PS80 introduced an electrically active interfacial contribution that amplified low-frequency permittivity at high filler loadings but made the permittivity more frequency-dependent. The piezoelectric response (between −20 pC/N and −25 pC/N) remained predominantly governed by the polymer phase, suggesting limited polarization played by BaTiO3. These results underlined the critical role of interfacial electrical properties in designing stable high-performance flexible PVDF-TrFE/BaTiO3 composites.
Broggio et al. (Sat,) studied this question.