Abstract
Solution casting and ultrasonic-assisted solution-cast methods were used to create polymer nanocomposites films based on polyvinyl alcohol (PVA)/polyvinyl pyrrolidone (PVP) filled with varying concentrations of BaTiO3 nanoparticles. The X-ray diffraction (XRD), Fourier-transform infrared (FT-IR), transmission electron microscope, and differential scanning calorimetry (DSC) were used to study the properties of the produced polymer nanocomposite samples. The properties of PVA/PVP-BaTiO3 nanocomposites, such as ac conductivity, dielectric constant, and dielectric loss, were investigated as a function of BaTiO3 concentration. XRD measurements demonstrate that the pure polymer blend is semi-crystalline and that the crystallinity degree (Xc) of the doped PVA/PVP mix films is lower than that of the pure blend. Significant variations in the FT-IR spectra demonstrate the interaction between the BaTiO3 ions and the PVA/PVP matrix. The DSC analysis demonstrates that the PVA/PVP has a single glass transition temperature (T-g), showing that the two polymers are miscible. In addition, when the amount of BaTiO3 NP's increased, the T-g of the nanocomposite films decreased. The AC conductivity spectra of all samples obey Jonscher's power law. For a better understanding of charge storage characteristics and conductivity relaxation, dielectric constant and loss investigations have been carried out. The PVA/PVP mixed with 1.5 wt% BaTiO3 nanofiller achieves a maximum ionic conductivity of similar to 8.57 x 10(-5) S/cm. In this investigation, which introduced a novel approach, the complex permittivity revealed that the real part value of the dielectric constant (epsilon') for all samples was much bigger than the imaginary part (epsilon '') value. These results are predicted to have a significant influence on a variety of applications, including polymer organic semiconductors, energy storage, polymer solar cells, and nanoelectronics.