Accuracy of the spin sum rule in XMCD for the transition-metal L edges from manganese to copper

被引:169
作者
Piamonteze, Cinthia [1 ]
Miedema, Piter [2 ]
de Groot, Frank M. F. [2 ]
机构
[1] Paul Scherrer Inst, Swiss Light Source, CH-5232 Villigen, Switzerland
[2] Univ Utrecht, NL-3584 CA Utrecht, Netherlands
来源
PHYSICAL REVIEW B | 2009年 / 80卷 / 18期
基金
美国国家科学基金会;
关键词
charge transfer states; cobalt; copper; core levels; crystal field interactions; exchange interactions (electron); ground states; iron; magnetic circular dichroism; manganese; nickel; spin-orbit interactions; valence bands; X-ray absorption spectra; MAGNETIC-CIRCULAR-DICHROISM; X-RAY-ABSORPTION; BRANCHING RATIO; DIPOLE TERM; SPECTROSCOPY; STATE; PROBE; NI;
D O I
10.1103/PhysRevB.80.184410
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The effective spin sum rule is widely used in the quantitative analysis of x-ray magnetic circular dichroism spectra. Here, this important, though imperfect, sum rule is reviewed with a detailed analysis of the various sources for errors and deviations. The simulations confirm that the final state effects of the core level spin-orbit coupling and the core-valence exchange interactions (multiplet effects) are linearly related with the effective spin sum-rule error. Within the charge transfer multiplet approach, we have analyzed these effects, in combination with the interactions affecting the magnetic ground state, including the crystal field strength, the charge transfer effects, the exchange (magnetic) field, and the 3d spin-orbit coupling. We find that for the late transition-metal systems, the error in the effective spin moment is between 5% and 10%, implying that for covalent and/or metallic systems the effective spin sum rule is precise to within 5-10 %. The error for 3d(5) systems is similar to 30% and for 3d(4) systems, the error is very large, implying that, without further information, the derived effective spin sum-rule values for 3d(4) systems have no meaning.
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页数:12
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