Taming Negative-Ion Resonances using Non-Local Exchange- Correlation Functionals

26 February 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Characterization of negative ion resonances poses a fundamental challenge to density functional methods due to the unbound nature of resonances. We overcome this challenge by proposing one-particle non-local exchange-correlation (xc) potentials combining the exact-exchange (EXX) and the random phase approximation (RPA) correlation potentials. The negative ion resonances are identified by perturbing the real-Hermitian non-local xc potentials using complex absorbing local-potentials. Our studies show that the non-local EXX+RPA potential significantly enhances the description of positions and widths of negative ion resonance-states compared to potentials that include EXX only or include static polarization effects only. The use of low-scaling algorithms reduces the computational scaling of RPA potential thereby providing a practical solution to resonance-state characterization within the density functional framework. The theoretical framework and underlying assumptions required for combining real Hermitian non-local xc potentials with complex local potentials are discussed.

Keywords

DFT
Negative ion resonances

Supplementary materials

Title
Description
Actions
Title
Supporting Information
Description
Basis-set studies and resonance-state trajectories
Actions

Comments

Comments are not moderated before they are posted, but they can be removed by the site moderators if they are found to be in contravention of our Commenting Policy [opens in a new tab] - please read this policy before you post. Comments should be used for scholarly discussion of the content in question. You can find more information about how to use the commenting feature here [opens in a new tab] .
This site is protected by reCAPTCHA and the Google Privacy Policy [opens in a new tab] and Terms of Service [opens in a new tab] apply.