Theoretical investigation of orbital alignment of x-ray-ionized atoms in exotic electronic configurations
Laura Budewig, Sang-Kil Son, Robin Santra

TL;DR
This paper provides a theoretical analysis of orbital alignment in x-ray-ionized atoms, using improved electronic-structure calculations to understand how linearly polarized x rays influence transient ions and their subsequent decay processes.
Contribution
It introduces an enhanced theoretical framework combining first-order many-body perturbation theory with Hartree-Fock-Slater calculations to accurately predict orbital alignment in exotic electronic configurations.
Findings
Improved transition energy calculations with first-order corrections.
Quantitative analysis of orbital alignment parameters for argon.
Insights into the evolution of orbital alignment during Auger-Meitner decay.
Abstract
We theoretically study orbital alignment in x-ray-ionized atoms and ions, based on improved electronic-structure calculations starting from the Hartree-Fock-Slater model. We employ first-order many-body perturbation theory to improve the Hartree-Fock-Slater calculations and show that the use of first-order-corrected energies yields significantly better transition energies than originally obtained. The improved electronic-structure calculations enable us also to compute individual state-to-state cross sections and transition rates and, thus, to investigate orbital alignment induced by linearly polarized x rays. To explore the orbital alignment of transiently formed ions after photoionization, we discuss alignment parameters and ratios of individual state-resolved photoionization cross sections for initially neutral argon and two exotic electronic configurations that may be formed during…
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