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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Multiferroic Behavior of Lead-free AlFeO3 and Mn, Nb Doped Compositions

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Autor(es):
Santos, G. M. [1] ; Silva, D. M. [1] ; Freitas, V. F. [1] ; Dias, G. S. [1] ; Coelho, A. A. [2] ; Pal, M. [3] ; Santos, I. A. [1] ; Cotica, L. F. [3, 1] ; Guo, R. [3] ; Bhalla, A. S. [3]
Número total de Autores: 10
Afiliação do(s) autor(es):
[1] Univ Estadual Maringa, Dept Phys, Maringa, Parana - Brazil
[2] Univ Estadual Campinas, Inst Fis Gleb Wataghin, Campinas, SP - Brazil
[3] Univ Texas San Antonio, Dept Elect & Comp Engn, San Antonio, TX 78249 - USA
Número total de Afiliações: 3
Tipo de documento: Artigo Científico
Fonte: Ferroelectrics; v. 460, n. 1, p. 108-116, FEB 17 2014.
Citações Web of Science: 6
Resumo

The lead-free AlFeO3-based compounds are attractive multiferroic materials, as those present piezoelectricity and ferrimagnetism at low temperatures. In this work the synthesis and ferroic properties of AlFeO3-based ceramics were investigated. Stoichiometric proportions of the precursors - alpha-Fe2O3 and alpha-Al2O3 - were milled and sintered to obtain AlFeO3 ceramics. Also, AlFeO3 ceramics doped with 2at% of Nb2O5 or MnO2 were sintered in oxygen flow at 1700K. The crystal structure of the samples was studied by X-ray diffraction. The diffractograms were refined by the Rietveld method. The results obtained from refinements showed an orthorhombic symmetry with space group Pna2(1). Dielectric, ferroelectric and magnetic investigations suggested a magnetoelectric coupling between the electric and magnetic orderings at temperatures below similar to 160K for AlFeO3, Al(Fe0.98Nb0.02)O-3 and Al(Fe0.98Mn0.02)O-3, where the compositions show the ferromagnetic and ferroelectric ordering. (AU)

Processo FAPESP: 08/04025-0 - Materiais multifuncionais multiferróicos nanoestruturados: síntese, propriedades, fenomenologia e aplicações
Beneficiário:José Antonio Eiras
Modalidade de apoio: Auxílio à Pesquisa - Temático