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UNIVERSIDADE ESTADUAL DE MARINGÁ - Pfi.uem.br

UNIVERSIDADE ESTADUAL DE MARINGÁ - Pfi.uem.br

UNIVERSIDADE ESTADUAL DE MARINGÁ - Pfi.uem.br

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Abstract<<strong>br</strong> />

Multiferroic magnetoelectric materials have attracted much attention of<<strong>br</strong> />

the theoretical and experimentalist researchers because they can present, in<<strong>br</strong> />

the same phase, ferroelectric and magnetic orderings. Among them, BiFeO3 is<<strong>br</strong> />

one of the most promising candidate for practical applications, whereas it<<strong>br</strong> />

presents high ferroelectric and antiferromagnetic ordering temperatures. The<<strong>br</strong> />

high electrical conductivity and the low dielectric permittivity are the main<<strong>br</strong> />

problems of working with BiFeO3, beyond the difficult for obtaining single<<strong>br</strong> />

phased materials. For solving these problems, process BiFeO3 with others<<strong>br</strong> />

perovskite structured materials that present high dielectric permittivities, like<<strong>br</strong> />

PbTiO3 and BaTiO3, seems to be an adequate alternative.<<strong>br</strong> />

Taking in mind this assumptions, in this work we processed, by<<strong>br</strong> />

high-energy ball milling, samples of the (x)BiFeO3-(1-x)BaTiO3 system, with 0,9<<strong>br</strong> />

≥ x ≥ 0,6, focusing the improvement of the BiFeO3 ferroic properties. The<<strong>br</strong> />

structural and microstructural characterizations had showed the formation of<<strong>br</strong> />

single phase perovskite structured materials. These samples have<<strong>br</strong> />

predominantly the R3c space group. The mean particle sizes of powders<<strong>br</strong> />

reached the nano scale, while the ceramics presented high densification rates<<strong>br</strong> />

with relatively homogeneous grains morphologies. All the processed materials<<strong>br</strong> />

showed antiferromagnetic and ferroelectric orderings at room temperature,<<strong>br</strong> />

which dielectric permittivities higher than that presented by the BiFeO3<<strong>br</strong> />

compound.<<strong>br</strong> />

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