X-ray absorption and dichroism of transition metals and their compounds

622Citations
Citations of this article
285Readers
Mendeley users who have this article in their library.
Get full text

Abstract

This review presents an overview of the X-ray absorption spectra of 3d transition metals and their compounds. The emphasis is on the description of the X-ray absorption process and the various routes to interpret the results within the framework of their electronic structure. This also includes the use of polarization dependent measurements which are particularly used for the study of the magnetic structure. Emphasis will be given to the metal 2p spectra for which the obtainable resolution has been greatly improved over the last 10 years. The interpretation of 2p core spectra, photoemission as well as absorption, is dominated by short range models, such as the Anderson impurity model. It has been shown that 2p X-ray absorption is relatively insensitive to charge transfer effects which simplifies the analysis. The interpretation with a ligand field multiplet model accounts well for the observed spectra and due to its simplicity this model yields accurate and well defined electronic structure parameters. For the Is X-ray absorption spectra, of the metals as well as of the ligands, it has been shown that they correspond closely to the unoccupied density of states as determined from single particle schemes using either band structure methods or real space multiple scattering. A number of potentially important effects beyond this interpretation will be discussed. Overviews will be given of the published X-ray absorption results for the metal 2p, the metal Is and the ligand Is spectra. © 1994 - Elsevier Science B.V. All rights reserved.

Cite

CITATION STYLE

APA

De Groot, F. M. F. (1994). X-ray absorption and dichroism of transition metals and their compounds. Journal of Electron Spectroscopy and Related Phenomena. Elsevier B.V. https://doi.org/10.1016/0368-2048(93)02041-J

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free