Structural, magnetic and magnetocaloric properties of Ag-doped La0.5Ca0.5-xAgxMnO3 compounds with 0 ≤ x ≤ 0.4

被引:73
|
作者
Smari, M. [1 ,2 ,3 ]
Walha, I. [1 ]
Dhahri, E. [1 ]
Hlil, E. K. [2 ,3 ]
机构
[1] Univ Sfax, Fac Sci Sfax, Appl Phys Lab, Sfax 3000, Tunisia
[2] CNRS, Inst Neel, F-38042 Grenoble 9, France
[3] Univ Grenoble 1, F-38042 Grenoble 9, France
关键词
Perovskite manganite; Magnetocaloric effect; Charge ordering; RCP factor; ROOM-TEMPERATURE; NEUTRON-DIFFRACTION; PHASE-SEPARATION; REFRIGERATION; TRANSITION; MAGNETORESISTANCE; DIAGRAM;
D O I
10.1016/j.jallcom.2013.07.104
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
Structural, magnetic and magnetocaloric properties of manganites series with the La0.5Ca0.5-xAgxMnO3 (0.0 <= x <= 0.4) compounds were investigated. Samples were synthesized using the solid state reaction at high temperature and analyzed by XRD data based on the Rietveld refinement technique. Samples with x = 0.0, 0.1, 0.2, 0.3 and 0.4 crystallized in orthorhombic symmetry with Pnma space group. Also, Magnetizations measurements were performed to investigate magnetic properties. Transition from ferromagnetic (FM) to charge ordered antiferromagnetic (CO-AFM) phases at low temperature is observed for Ag-free La0.5Ca0.5MnO3. Compounds with x = 0.2, 0.3 and 0.4, do not exhibit this transition, and only FM metallic phases are observed. The Curie temperature T-C increases with increasing Ag amount from 222 K (for x = 0.0) to 264 K (for x = 0.2). While x > 0.2, T-C remains substantially constant. Magnetic entropy change (Delta S-M) was estimated from isothermal magnetization data. Parent compound (x = 0.0) exhibits both normal (negative DSM) and inverse (positive Delta S-M) magnetocaloric effects at TC and TCO, respectively. However, all the Ag doped samples show only normal magnetocaloric effect at T-C. The Largest MCE occurs for sample with x = 0.4 (Delta S-M = 3.27 J kg(-1) K-1, DH = 5 T) for which largest relative cooling power (RCP = 229.27 J kg(-1), Delta H = 5 T) is reached as well. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:564 / 571
页数:8
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