X-ray absorption and x-ray magnetic dichroism study on Ca3CoRhO6 and Ca3FeRhO6

被引:100
作者
Burnus, T. [1 ]
Hu, Z. [1 ]
Wu, Hua [1 ]
Cezar, J. C. [2 ]
Niitaka, S. [3 ,4 ]
Takagi, H. [3 ,4 ,5 ]
Chang, C. F. [1 ]
Brookes, N. B. [2 ]
Lin, H. -J. [6 ]
Jang, L. Y. [6 ]
Tanaka, A. [7 ]
Liang, K. S. [6 ]
Chen, C. T. [6 ]
Tjeng, L. H. [1 ]
机构
[1] Univ Cologne, Inst Phys 2, D-50937 Cologne, Germany
[2] European Synchrotron Radiat Facil, F-38043 Grenoble, France
[3] RIKEN, Inst Phys & Chem Res, Wako, Saitama 3150198, Japan
[4] Japan Sci & Technol Agcy, CREST, Kawaguchi, Saitama 3320012, Japan
[5] Univ Tokyo, Dept Adv Mat Sci, Chiba 2778581, Japan
[6] Natl Synchrotron Radiat Res Ctr, Hsinchu 30077, Taiwan
[7] Hiroshima Univ, Dept Quantum Matter, ADSM, Higashihiroshima 7398530, Japan
关键词
D O I
10.1103/PhysRevB.77.205111
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
By using x-ray absorption spectroscopy at the Rh L-2,L-3, Co L-2,L-3, and Fe L-2,L-3 edges, we find a valence state of Co2+/Rh4+ in Ca3CoRhO6 and of Fe3+/Rh3+ in Ca3FeRhO6. X-ray magnetic circular dichroism spectroscopy at the Co L-2,L-3 edge of Ca3CoRhO6 reveals a giant orbital moment of about 1.7 mu(B), which can be attributed to the occupation of the minority-spin d(0)d(2) orbital state of the high-spin Co2+ (3d(7)) ions in trigonal prismatic coordination. This active role of the spin-orbit coupling explains the strong magnetocrystalline anisotropy and Ising-type magnetism of Ca3CoRhO6.
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页数:6
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