Structural, electrical, and magnetic transport properties of La0.72Ca0.28Mn1_xCrxO3 (0=??????? x =0.06) ceramics

被引:4
|
作者
Gao, Yan [1 ]
Ma, Ji [1 ]
Chen, Qingming [1 ]
Zhang, Hui [1 ]
Kong, Lingde [3 ]
Dong, Kun [4 ]
Zhong, Wenhong [4 ]
Yang, Sheng'an [2 ]
机构
[1] Kunming Univ Sci & Technol, Fac Mat Sci & Engn, Kunming 650093, Yunnan, Peoples R China
[2] Kunming Univ Sci & Technol, Fac Met & Energy Engn, Kunming 650093, Yunnan, Peoples R China
[3] Kunming Inst Phys, Kunming 650223, Yunnan, Peoples R China
[4] Kunming Univ Sci & Technol, Res Ctr Anal & Measurement, Kunming 650093, Yunnan, Peoples R China
基金
中国国家自然科学基金;
关键词
Polycrystalline La0.72Ca0.28Mn0.98Cr0.02O3; Temperature coefficient of resistivity (TCR); Magnetoresistance (MR); LA2/3CA1/3MNO3; THIN-FILMS; TEMPERATURE-COEFFICIENT; MAGNETOCALORIC PROPERTIES; MAGNETORESISTANCE; MANGANITES; CR; RESISTIVITY; TI;
D O I
10.1016/j.ceramint.2022.04.011
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
To obtain comprehensive materials with both high temperature coefficient of resistivity (TCR) and magnetoresistance (MR) at low magnetic fields, polycrystalline La0.72Ca0.28Mn1_xCrxO3 (x = 0, 0.02, 0.04, 0.06) ceramics were prepared herein by sol-gel method. Electronic configuration of Cr3+ ions is similar to that of Mn4+ ions, therefore, successive substitution of Mn with Cr increases electrical resistivity and decreases metal-insulator transition temperature of ceramics, even yielding hump-like feature for Cr-rich (x = 0.06) samples. The best TCR (28.50%.K_1) and MR (72.37%) values were obtained simultaneously at Cr dopant content of 0.02 (La0.72Ca0.28Mn1_xCrxO3). Strong response of the material to temperature and magnetic field was caused by minimal symmetry of orthorhombic structure and the most robust Jahn-Teller distortion. With increasing Cr content, Mn3+/Mn4+ or Mn3+/Cr3+ double exchange was diluted, and Cr3+/Cr3+ or Cr3+/Mn4+ superexchange was promoted. However, the internal competition effect was not conducive to the improvement of material properties.
引用
收藏
页码:21187 / 21193
页数:7
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