Actinide and lanthanide speciation with high-energy resolution X-ray techniques

被引:42
|
作者
Vitova, T. [1 ]
Denecke, M. A. [1 ]
Goettlicher, J. [2 ]
Jorissen, K. [3 ]
Kas, J. J. [3 ]
Kvashnina, K. [4 ]
Pruessmann, T. [1 ]
Rehr, J. J. [3 ]
Rothe, J. [1 ]
机构
[1] Karlsruhe Inst Technol, Inst Nucl Waste Disposal, POB 3640, D-76021 Karlsruhe, Germany
[2] Karlsruhe Inst Technol, Inst Synchrotron Radiat, D-76021 Karlsruhe, Germany
[3] Univ Washington, Dept Phys, Seattle, WA 98195 USA
[4] ESRF, F-38043 Grenoble, France
关键词
D O I
10.1088/1742-6596/430/1/012117
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
High-energy resolution X-ray absorption spectroscopy (HR-XAS) and Resonant inelastic X-ray scattering (RIXS) combined with quantum theoretical tools are gaining importance for understanding electronic and coordination structures of actinide (An) and lanthanide (Ln) materials. HR-XAS is successfully used to remove lifetime broadening by registering the partial fluorescence yield emitted by the sample, thereby yielding highly resolved X-ray absorption near edge structure spectra (HR-XANES), which often display resonant features not observed in conventional XANES. We demonstrate the structural characterization capabilities of these novel techniques by comparative discussion of U M-4/L-3-HR-XANES and L-3-valence band RIXS (L-3-VB-RIXS) spectra of two model U(VI) minerals. We show that the ab initio multiple scattering theory based code FEFF9.5 is an effective tool for calculations of An and Ln L-3-HR-XANES and L-3-RIXS spectra as it successfully reproduces dipole and quadrupole transitions in the same spectrum.
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页数:4
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