Abstract
A theoretical description of spin-resolved (core-valence-valence) Auger electron spectroscopy is presented. The approach is derived on the basis of a fully relativistic description of the electronic structure of magnetic materials. As a consequence, spontaneous exchange splitting as well as spin-orbit coupling—two possible and important sources for a spin-polarization of Auger electrons—are accounted for on the same level. This is demonstrated by application to paramagnetic fcc Pd and ferromagnetic bcc Fe. In both cases spin-resolved Auger electron spectra are presented and discussed emphasizing the role of the spin-orbit coupling. Comparison is made with available experimental data as far as possible.
- Received 12 April 2000
DOI:https://doi.org/10.1103/PhysRevB.62.10051
©2000 American Physical Society