Resonant x-ray spectroscopy of uranium intermetallics at the M4,5 edges of uranium

被引:39
|
作者
Kvashnina, K. O. [1 ,2 ]
Walker, H. C. [3 ]
Magnani, N. [4 ]
Lander, G. H. [4 ]
Caciuffo, R. [4 ]
机构
[1] Helmholtz Zentrum Dresden Rossendorf, Inst Resource Ecol, D-01314 Dresden, Germany
[2] European Synchrotron ESRF, F-38000 Grenoble, France
[3] Rutherford Appleton Lab, ISIS Neutron & Muon Source, Didcot OX11 0QX, Oxon, England
[4] European Commiss, Joint Res Ctr, Directorate Nucl Safety & Secur, Postfach 2340, D-76125 Karlsruhe, Germany
关键词
MAGNETIC NEUTRON-SCATTERING; HEAVY-FERMION COMPOUNDS; CRYSTAL-FIELD; ELECTRONIC-STRUCTURE; ACTINIDE COMPOUNDS; INTERMULTIPLET TRANSITIONS; PLUTONIUM INTERMETALLICS; 5F ORBITALS; ABSORPTION; EXCITATIONS;
D O I
10.1103/PhysRevB.95.245103
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We present resonant x-ray emission spectroscopic data from the uranium intermetallics UPd3, USb, USn3, and URu2Si2 at the M-4,M-5 edges of uranium, and we compare the data to those from the well-localized 5f(2) semiconductor UO2. The technique is especially sensitive to any oxidation of the surface, and this was found on the USb sample, thus preventing a good comparison with a material known to be 5f(3). We have found a small energy shift between UO2 and UPd3, both known to have localized 5f(2) configurations, which we ascribe to the effect of conduction electrons in UPd3. The spectra from U Pd-3 and URu2Si2 are similar, strongly suggesting a predominant 5f(2) configuration for URu2Si2. The valence-band resonant inelastic x-ray scattering provides information on the UP3 transitions (at about 18 eV) between the U 5f and U 6p states, as well as transitions of between 3 and 7 eV from the valence band into the unoccupied 5f states. These transitions are primarily involving mixed ligand states (O 2p or Pd, Ru 4d) and U 5f states. Calculations are able to reproduce both of these low-energy transitions reasonably well.
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页数:10
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