Feshbach–Fano approach for calculation of Auger decay rates using equation-of-motion coupled-cluster wave functions. II. Numerical examples and benchmarks
X-ray photon absorption leads to the creation of highly excited species, which often decay through the Auger process. The theoretical treatment of Auger decay is challenging because of the resonance nature of the initial core-excited or core-ionized states and the continuous nature of the ejected el...
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Veröffentlicht in: | The Journal of chemical physics 2021-02, Vol.154 (8), p.084125-084125, Article 084125 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | X-ray photon absorption leads to the creation of highly excited species, which often decay through the Auger process. The theoretical treatment of Auger decay is challenging because of the resonance nature of the initial core-excited or core-ionized states and the continuous nature of the ejected electron. In Paper I [W. Skomorowski and A. I. Krylov, J. Chem. Phys. 154, 084124 (2021)], we have introduced a theoretical framework for computing Auger rates based on the Feshbach–Fano approach and the equation-of-motion coupled-cluster ansätze augmented with core–valence separation. The outgoing Auger electron is described with a continuum orbital. We considered two approximate descriptions—a plane wave and a Coulomb wave with an effective charge. Here, we use the developed methodology to calculate Auger transition rates in core-ionized and core-excited benchmark systems (Ne, H2O, CH4, and CO2). Comparison with the available experimental spectra shows that the proposed computational scheme provides reliable ab initio predictions of the Auger spectra. The reliability, cost efficiency, and robust computational setup of this methodology offer advantages in applications to a large variety of systems. |
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ISSN: | 0021-9606 1089-7690 |
DOI: | 10.1063/5.0036977 |