Effect of Bi2O3 nanoparticle loading on the structural, thermal, and dielectric properties of epoxy nanocomposites
摘要
This study comprehensively investigates the structural, thermal, and dielectric properties of epoxy/Bi2O3 nanocomposites with varying Bi2O3 loadings (0–10 wt%). X-ray diffraction (XRD) analysis revealed a transition from amorphous to semicrystalline behavior at ≥ 1 wt% Bi2O3. The crystallite size reduced from 34 to 19 nm and the lattice strain increased (4.65–7.45 × 10−3) at higher loadings. Scanning electron microscopy (SEM) confirmed progressive nanoparticle agglomeration above 1 wt%. Fourier-transform infrared spectroscopy (FTIR) showed epoxy functional groups with small variation after Bi2O3 inclusion. Thermal analysis demonstrated reduced glass transition temperatures (84–60 °C). Additionally, the activation energies (Ea) exhibited a non-monotonic trend (399–367 kJ/mol). Dielectric studies revealed frequency- and temperature-dependent polarization mechanisms, with interfacial (Maxwell-Wagner-Sillars) relaxation peaks shifting to higher frequencies upon heating (Ea = 0.83–1.15 eV). AC conductivity followed Jonscher’s law, with exponent s (0.71–1.38) reflecting a transition from correlated barrier hopping to near-free conduction. DC conductivity activation energy (EDC) decreased systematically (1.30–1.11 eV) with Bi2O3 loading. These findings collectively elucidate the interplay between nanofiller dispersion, interfacial dynamics, and multifunctional performance in epoxy/Bi2O3 nanocomposites for dielectric and thermal applications.