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In the present work, composite ceramics of BaTiO3 with La0.08Pb0.92Ti0.20Zr0.80O3 were prepared from powders synthesized by two different methods: (a) PLZT@BT ceramics from core-shell powders with PLZT-core and BaTiO3 shell and (b) PLZT-BT ceramic composites from mixed PLZT and BaTiO3 powders. In core-shell ceramics, a thin conductive layer of BaPbO3 was formed that resulted in an increased effective permittivity with relatively low losses (tan δ<0.7 in kHz regions). The extrinsic contributions play an important role in both ceramics, but they are more evident in core-shell samples due to the large number of interfaces. These results show that novel functional properties can be tailored by the controlled chemical reaction at interfaces. [ABSTRACT FROM AUTHOR]

In the present work, composite ceramics of ferroelectric BaTiO3 (BT) with magnetic αFE2O3 were prepared from powders synthesized by two different methods: (a) core-shell powders of FE2O3@BT and (b) FE2O3-BT composites from mixed powders with the same composition. The M(H) loops at room temperature show a "wasp-waisted" character, with multiple components, determined as result of the formation of magnetic phases with contrasting coercivities (hard BaFe12O19 and soft Ba12Ti28Fe15O84 phases) in different ratios, as indicated by the magnetic firstorder- reversal curves analysis. The core-shell composite ceramics generally showed slightly improved dielectric properties and smaller conductivity. The high field properties of composite ceramics show a strong nonlinearity in both cases, together with a reduction of zero field permittivity, making from these composites possible tunable materials interesting for applications. Their multifunctional character is enhanced by the presence of a complex magnetic character with soft/ hard components. [ABSTRACT FROM AUTHOR]

The influence of the oxygen vacancies on the dielectric response of BaZr0.10Ti0.90O3 ceramics prepared by solid-state reaction and sintered at 1400 °C for 2 h was investigated. The as-sintered ceramic exhibits a giant relaxation with a shift of the transition temperature from ∼85 °C to above 170 °C in the frequency ranges of 1 Hz-100 kHz, with high losses above unity and two components in the complex impedance plot. A complex dielectric relaxation response, with at least two thermally activated defect mechanisms with activation energies of ∼0.2 eV below the transition temperature and ∼0.7 eV for higher temperatures in the range of 85 °C-170 °C was determined. The observed giant relaxation is an extrinsic effect related to the oxygen deficiency, inhomogeneous distributed in the ceramic grain and not to the relaxor behavior of this system. After a post-annealing treatment at 1000 °C for 50 h, the dielectric response is completely changed: the permittivity vs. temperature dependences present maxima located at around Tm ≈ 90 °C, with almost no frequency dispersion. The conductivity spectra remained almost unchanged after the annealing, showing that the level of oxygen deficiency in this case is related to dielectric relaxations and not to the ac-conductivity dispersion. Two thermally activated dielectric relaxation processes were still identified, but with activation energies of ∼2.7 eV below the transition temperature and of ∼0.87 eV for higher temperatures in the range of 85 °C-170 °C. The high frequency relaxation process is almost suppressed by the reoxidation and its activation energy increased with more than one order in magnitude. One single component in the complex impedance plot found after reoxidation shows that the annealing allowed the homogenization of the oxygen level within the ceramic grains. [ABSTRACT FROM AUTHOR]