Ligand field effects on the multiplet structure of the U4f XPS of UO2

Abstract

Ab initio, fully relativistic four component theory was used to determine atomic and interatomic many-body effects for the U4f X-ray photoelectron spectrum of an embedded UO8-12 cluster representing UO2. Many-body effects were included through the use of configuration interaction wavefunctions that allow the mixing of XPS allowed and XPS forbidden configurations. Charge transfer configurations were not included. This work extends our earlier studies on simulations of the 4f XPS for the free U4+ cation. While the main XPS features are similar in both cases, ligand field effects changed the multiplet structure in important ways that better simulated experimental data for UO2. Neither initial nor final state covalency significantly reduced the 4f–5f exchange integrals, and the differences between the atom and cluster model were due to ligand field splitting of the 5f band and increased distributions of intensity from XPS allowed to XPS forbidden peaks. The prominent 7eV satellites associated with UO2 were absent in the simulations, which provided further evidence that these satellites are due to charge transfer and not other interatomic effects.