Structural and magnetic properties of the new brownmillerite oxides La1-xNaxSrMn2O5+δ (0.1 ≤x ≤ 0.3)

被引:2
|
作者
Mohamed, M. [1 ]
Rammeh, N. [2 ]
Mokhtar, F. [2 ]
Kabadou, A. [1 ]
Van der Lee, A. [3 ]
机构
[1] Fac Sci Sfax, Dept Chim, Lab Sci Mat & Environm, Sfax 3000, Tunisia
[2] Ctr Natl Rech Sci Mat, Lab Physicochimie Mat Mineraux & Leurs Applicat, Hammam Lif 2050, Tunisia
[3] Univ Montpellier 2, Inst Europeen Membranes, F-34095 Montpellier 5, France
关键词
Ceramics; Magnetic materials; Magnetometer; Magnetic properties; Powder diffraction; PHASE-SEPARATION; MAGNETORESISTANCE; TEMPERATURE; DEPENDENCE;
D O I
10.1016/j.matchemphys.2015.09.016
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Na-doped brownmillerite oxides La1-xNaxSrMn2O6 (x = 0, 0.1, 0.2 and 0.3) were synthesized by the solid state reaction method at high temperature. The structural and magnetic properties of the samples were investigated by X-ray diffraction and magnetization experiments. The results from X-ray diffraction analysis showed that all samples were single phase and crystallized in the orthorhombic system, with space group Pnma. This structure can be described as an oxygen-deficient perovskite, resulting in a sequence of regular alternating layers of corner-sharing BO6 octahedra (O) and BO4 tetraedra (T) according to axis b. The results from magnetization versus temperature measurements in a magnetic applied field of 0.05 T indicated that the samples underwent a paramagnetic ferromagnetic transition with decreasing temperature. The Curie temperature T-c decreased from 365 to 345 K with Na content. An electronic phase separation model considering the formation of ferromagnetic clusters in the antiferromagnetic matrix was proposed to interpret the observed magnetization results for the Na-substituted samples. Overall, the present study provided an effective approach to achieve new functional materials based on naturally occurring layered systems such as La1-xNaxSrMn2O5+delta, for possible application in the spintronics industry. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:49 / 56
页数:8
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