Analysis of the magnetic transition and magnetocaloric effect in Mn5Ge2.9Ag0.1 compound

被引:17
作者
Si, Xiaodong [1 ,2 ]
Liu, Yongsheng [1 ]
Zhang, Zhanxian [1 ]
Ma, Xinxiu [1 ]
Lin, Jia [1 ]
Luo, Xiaojing [1 ]
Zhong, Yunbo [3 ]
Si, Hongtao [4 ]
机构
[1] Shanghai Univ Elect Power, Inst Solar Energy, Shanghai 200090, Peoples R China
[2] Southeast Univ, Sch Energy & Environm, Nanjing 210096, Jiangsu, Peoples R China
[3] Shanghai Univ, Sch Mat Sci & Engn, Shanghai 200444, Peoples R China
[4] Chongqing Inst Geol & Mineral Resources, Chongqing 401120, Peoples R China
关键词
Mn5Ge3; Magnetocaloric effect; Curie temperature; Magnetic refrigeration; MAGNETOSTRUCTURAL PHASE-TRANSITIONS; HIGH-ENTROPY ALLOYS; CRITICAL-BEHAVIOR; MN; CO; TRANSFORMATION; SUBSTITUTION; TEMPERATURE;
D O I
10.1016/j.jallcom.2019.04.206
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
Here we investigate analytical models to understand magnetic and magnetocaloric properties of Mn5Ge2.9Ag0.1 compound prepared by arc-melting method. The Mn5Ge2.9Ag0.1 alloy, undergoing a second-order transition, shows a maximum magnetic entropy change of about 6.86 J/kgK and the relative cooling power (RCP) value of 386 J/kg at 298 K under a field change of 5T. Based on a phenomenological model, the magnetocaloric properties obtained from temperature-dependent magnetization data are in good agreement with the experimental results. To give a better understanding of magnetic transition and the effective magnetic entropy change, we quantify the coupling of lattice energy and electronic energy contribution to the effective magnetic entropy change from a Landau theory plus Bean-Rodbell model. Interestingly, the coupling of lattice energy and electronic energy presents a positive value of up to 4.5% of the effective magnetic entropy change, producing a deleterious impact on the effective magnetic entropy change. The results suggest that the Mn5Ge2.9Ag0.1 system could be a very attractive material for room-temperature magnetic refrigeration applications. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:304 / 313
页数:10
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