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Valence, hybridization of electronic states and magnetic properties of La0.7Ca0.3Mn1-xScxO3 (x=0.0; 0.03, and 0.05) manganites
被引:5
|作者:
Ulyanov, A. N.
[1
]
Yang, Dong-Seok
[2
]
Shin, Hyun-Joon
[3
]
Kim, Ki-jeong
[3
]
Vasiliev, A. V.
[1
]
Savilov, S. V.
[1
]
机构:
[1] Lomonosov Moscow State Univ, Dept Chem, Moscow 119991, Russia
[2] Chungbuk Natl Univ, Dept Phys Educ, Cheongju 28644, South Korea
[3] POSTECH, Pohang Accelerator Lab, Pohang 37673, South Korea
基金:
俄罗斯基础研究基金会;
关键词:
B-site doped manganites;
Electron structure;
Curie temperature;
XAFS;
SUBSTITUTED LANTHANUM MANGANITES;
LOCAL-STRUCTURE;
MN-SITE;
K-EDGE;
BEHAVIOR;
MAGNETORESISTANCE;
DESTRUCTION;
PATHWAY;
D O I:
10.1016/j.jallcom.2019.04.290
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:
X-ray absorption spectroscopy at Mn K- and L-edges, and at O K-edge, combined with the x-ray diffraction and magnetization measurements are performed to study the electron structure of La0.7Ca0.3Mn1-xScxO3 (x = 0.0; 0.03, and 0.05) perovskites. Substitution of manganese by scandium decreases Curie temperature, Tc, and increases lattice parameters because of the different electron configuration and radii of trivalent manganese and scandium ions. The Tc decrease is explained by the change of level of hybridization of O 2p and Mn 3d states. This is manifested by the parallel shift of O K-edge, change of intensity of 2p(3/2) and 2p(1/2) spectrum lines and T-C with x increase. Fourier transform of the EXAFS spectra shows a change of local crystal structure caused by the larger Sc3+ than the Mn3+ ions. (c) 2019 Elsevier B.V. All rights reserved.
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页码:223 / 226
页数:4
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