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Calculation of multipole transitions at the Fe K pre-edge through p-d hybridization in the Ligand Field Multiplet model

M.-A. Arrio, S. Rossano, Ch. Brouder, L. Galoisy and G. Calas

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For the first time, commonly unaccessible local electronic structure parameters of Fe2+ and Fe3+ in minerals are derived from the calculation of the pre-edge features of X-ray absorption spectra at the Fe K edge. The Ligand Field Multiplet approach is used to calculate the eigenstates of the ions and the absolute intensities of the electric-quadrupole and dipole transitions involved in the pre-edge. For ions in tetrahedral symmetry, a new model for p-d hybridization is developed. The degree of admixture between 3d and 4p levels is derived and local structure parameters (crystal field, bond covalency) are obtained.


PACS

71.70.Ch Crystal and ligand fields

78.70.Dm X-ray absorption spectra

Subjects

Condensed matter: electrical, magnetic and optical

Dates

Issue 4 (15 August 2000)

Received 2 May 2000, accepted for publication 13 June 2000, in final form 13 June 2000



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