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Title: The effect of symmetry on the U L3 NEXAFS of octahedral coordinated uranium( vi )

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.4978481· OSTI ID:1372961
ORCiD logo [1];  [2];  [3]
  1. Univ. of North Texas, Denton, TX (United States). Dept. of Chemistry
  2. Consultant, Austin, TX (United States)
  3. Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

We describe herein a detailed theoretical analysis of how distortions from ideal cubic or Oh symmetry to tetrahedral, D4h, symmetry affect the shape, in particular the width, of the U L3-edge NEXAFS for U(VI) in octahedral coordination. The full-width-half-maximum (FWHM) of the L3-edge white line decreases with increasing distortion from Oh symmetry. In particular, the FWHM of the white line narrows whether the tetragonal distortion is to compression or to extension. The origin of this decrease in the FWHM is analyzed in terms of the electronic structure of the excited levels arising from the unoccupied U(6d). The relative importance of ligand field and of spin-orbit effects is examined, where the dominant role of ligand field effects is established. Especially at higher distortions, the ligand splittings decrease rapidly and lead to an accelerated, quadratic decrease in the FWHM with increasing distortion. This is related to the increase of covalent character in the appropriate component of the Oh derived eg orbitals. Our ab initio theory uses relativistic wavefunctions for cluster models of the structures; empirical or semi-empirical parameters were not used to adjust prediction to experiment. A major advantage is that it provides a transparent approach for determining how the character and extent of the covalent mixing of the relevant U and O orbitals affect the U L3-edge white line.

Research Organization:
Pacific Northwest National Laboratory (PNNL), Richland, WA (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES). Chemical Sciences, Geosciences, and Biosciences Division
Grant/Contract Number:
AC05-76RL01830
OSTI ID:
1372961
Alternate ID(s):
OSTI ID: 1348037
Report Number(s):
PNNL-SA-123334; KC0302060
Journal Information:
Journal of Chemical Physics, Vol. 146, Issue 11; ISSN 0021-9606
Publisher:
American Institute of Physics (AIP)Copyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 8 works
Citation information provided by
Web of Science

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Cited By (4)

Consequences of realistic embedding for the L 2,3 edge XAS of α-Fe 2 O 3 journal January 2018
Analysis of X-ray adsorption edges: L 2,3 edge of FeCl 4 journal December 2017
Comparison of multireference ab initio wavefunction methodologies for X-ray absorption edges: A case study on [Fe(II/III)Cl 4 ] 2–/1– molecules journal March 2019
Cluster embedding of ionic systems: Point charges and extended ions journal July 2019