RESUMEN
In the present paper, the La0.8Ba0.1Bi0.1FeO3 powders were synthesized via the auto-combustion method. The optical, the positron annihilation spectroscopy and the gas sensing properties of our sample were investigated simultaneously. FTIR spectrum revealed the antisymmetric deformation vibrations of the Fe-O and Fe-O-Fe bonds inside the octahedron FeO6. The optical bandgap (Egap) of the La0.8Ba0.1Bi0.1FeO3 compound was found to be equal to 2.23 eV. We confirmed by the positron annihilation studies, the existence of open volume defects and vacancy sized defects, at the grain/interfaces between vacancy clusters and grains at the interfaces intersection (triple-lines). Notably, the La0.8Ba0.1Bi0.1FeO3 perovskite exhibits an excellent response toward acetone gas, with ultra-fast response and recovery times to some parts-per-billion (ppb) of this tested gas.
RESUMEN
In this work we synthesized the multifunctional (La0.8Ca0.2)0.4Bi0.6FeO3 material using a sol-gel process. Structural and morphologic investigations reveal a Pnma perovskite structure at room temperature with spherical and polygonal nanoparticles. A detailed study of the temperature dependence of the dielectric and electrical properties of the studied material proves a typical FE-PE transition with a colossal value of real permittivity at 350 K that allows the use of this material in energy storage devices. Thus, the investigation of the frequency dependence of the ac conductivity proves a correlated barrier hopping (CBH) conduction mechanism to be dominant in the temperature ranges of 150-170 K; the two observed Jonscher's power law exponents, s 1 and s 2 between 180 K and 270 K correspond to the observed dispersions in the ac conductivity spectra in this temperature region, unlike in the temperature range of 250-320 K, the small polaron tunnel (NSPT) was considered the appropriate conduction model.
RESUMEN
La1-2x Ba x Bi x FeO3 (0.00 ≤ x ≤ 0.20) nanoparticles were prepared by the auto-combustion method using glycine as a combustion fuel. X-ray diffractometry (XRD) measurements confirmed the orthorhombic structure of the synthesized compounds with the Pnma space group as a principal majority phase and showed the presence of a very minor secondary phase when x > 0.1. The nanosize criterion of the prepared compounds was confirmed from the crystallite size values calculated using the Williamson-Hall formalism. The relaxation process has been studied by the frequency dependence of the imaginary parts of impedance and modulus (Z'' and M'') which satisfied the Arrhenius law. Nyquist plots allowed us to obtain an adequate equivalent circuit involving the grains and grain boundary contributions. The activation energies calculated from Z'', M'' and the resistance of both contributions deduced from the Nyquist plots are found to be very similar. The conduction mechanism has been analyzed using the temperature dependence of the exponent Jonscher's power law parameter which confirms the NSPT conduction mechanism type for all compounds with an enhancement of the binding energy of the charge carrier (W H) with the substitution.
