Actinide and lanthanide speciation with high-energy resolution X-ray techniques
Author(s) -
Tonya Vitova,
Melissa A. Denecke,
Jörg Göttlicher,
Kevin Jorissen,
J. J. Kas,
Kristina O. Kvashnina,
T. Prüßmann,
J. J. Rehr,
Jörg Rothe
Publication year - 2013
Publication title -
journal of physics conference series
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.21
H-Index - 85
eISSN - 1742-6596
pISSN - 1742-6588
DOI - 10.1088/1742-6596/430/1/012117
Subject(s) - xanes , x ray absorption spectroscopy , scattering , resonant inelastic x ray scattering , absorption spectroscopy , lanthanide , spectroscopy , chemistry , spectral line , x ray spectroscopy , actinide , ab initio , electronic structure , atomic physics , analytical chemistry (journal) , materials science , inelastic scattering , physics , x ray raman scattering , optics , computational chemistry , inorganic chemistry , ion , chromatography , organic chemistry , quantum mechanics , astronomy
International audienceHigh-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 spectru
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