Alternative current conduction, dielectric behavior, transport properties and Mossbauer study of LaBaFe0.5Ti0.5MnO6-δ new compound

被引:4
|
作者
Ben Hafsia, A. L. [1 ]
Rammeh, N. [2 ]
Ferid, M. [2 ]
Errien, N. [3 ]
Greneche, J. M. [3 ]
Khitouni, M. [1 ]
机构
[1] Univ Sfax, Lab Chim Inorgan, Fac Sci Sfax, Ur Es 73 11, Sfax 802, Tunisia
[2] Ctr Natl Rech Sci Mat, Lab Physicochim Mat Mineraux & Leurs Applicat, BP 95, Hammam Lif 2050, Tunisia
[3] Univ Maine, CNRS, UMR 6283, IMMM, F-72085 Le Mans 9, France
关键词
Perovskite oxide; Sol-gel reaction; X-ray diffraction; Complex impedance; Ac conductivity; Conduction mechanism; Fe-57 Mossbauer spectrometry; COMPLEX IMPEDANCE ANALYSIS; ELECTRICAL-PROPERTIES; DOUBLE-PEROVSKITE; AC CONDUCTIVITY; RELAXATION; OXIDE; MAGNETORESISTANCE; YBACUFEO5+DELTA; TEMPERATURE; ADMITTANCE;
D O I
10.1016/j.jallcom.2016.11.112
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The new perovskite compound with formula LaBaFe0.5Ti0.5MnO6-delta was prepared by the sol-gel method using the citric acid route. The analysis of X-ray diffraction pattern using Le Bail method allows to conclude unambiguously that the sample exhibits single phase type cubic structure at room temperature. Electrical properties were studied using complex impedance spectroscopy as a function of frequency (100 Hz-7 MHz) at various temperatures (278-573 K). Impedance analysis has shown the grain contribution using an equivalent circuit model. The frequency dependence of the AC conductivity followed the universal power law variation. The values of activation energies obtained from the analysis of M '', conductivity data and equivalent circuit are too close and confirm that the sample behaves as a semiconductor. The plot of pre-exponent s versus temperature of the sample suggests that the conduction mechanism can be described using the non-overlapping small polaron tunneling model (NSPT) model. The Mossbauer measurements showed a paramagnetic behavior with the presence of only HS Fe3+ at 300 and 77 K. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:3310 / 3317
页数:8
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