Charge transfer processes and magnetoresistance in strontium ferromolybdate with dielectric barriers

Autor: Nikolay Kalanda, V. M. Garamus, Mikhail L. Zheludkevich, Nikolai A. Sobolev, L. V. Kovalev, Regine Willumeit
Jazyk: angličtina
Rok vydání: 2013
Předmět:
Zdroj: Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Popis: The Sr2FeMoO6-delta compound attracts the attention of researchers due to a high Curie temperature, large values of negative magnetoresistance at room temperature and a practically 100% spin polarization of conduction electrons. We have studied the role of grain boundaries on the electrical transport in Sr2FeMoO6-delta in applied magnetic fields up to 8 T. The compound was synthesized out of partially reduced SrFeO3-x, SrMoO4-y precursors (sample I). At the first oxidation stage upon annealing at 700K in argon with a partial oxygen pressure p(O-2)-10 Pa for 15 h (sample II), the internal structure of the Sr2FeMoO5.82 grains did not change. Sample II exhibits a mixed type of electrical conduction. In a magnetic field B its resistivity decreases without changing the mixed regime of charge transport, only shifting the temperature of minimum resistivity (T-mB) to lower values. At temperatures above TmB the conductivity is predominantly metallic, whereas below TmB down to 4.2K it is of semiconductor type. The increase of the annealing time up to 30 h (sample III) brings about an increase of the resistivity and the appearance of semiconductor-type conductivity at T 300-4.2 K, which indicates the formation of a continuous insulating interlayer between the grains. In a magnetic field, the resistivity decreases, with the conductivity changing from the semiconducting to a mixed one. In the latter case the charge transport can occur both through point metallic contacts and by means of spin-dependent tunneling across dielectric interlayers between Sr2FeMoO5.82 grains. (C) 2013 WILEY-VCH Verlag GmbH \& Co. KGaA, Weinheim
Databáze: OpenAIRE