Stabilization Method as a Tool for Electronic State Spectroscopy

We propose a new systematic approach to distinguish valence and diffuse electronically excited states of polyatomic molecules. This method applies the stabilization technique of Hazi and Taylor [<i>Phys. Rev. A</i> <b>1970</b>, 1 (1109)] to neutral excited states, using basis set diffuseness as the stabilization parameter. By monitoring how excited states behave under basis set contraction, one can differentiate valence states from Rydberg and mixed valence-Rydberg states, reducing the arbitrariness of previous strategies. Valence states remain stable, whereas the energies of Rydberg and mixed states vary. This approach is compatible with any electronic structure method. To illustrate its applicability, we characterize the singlet excited states of CCl<sub>4</sub>, HCOOH, and 2-chlorotoluene. This provides a valuable tool for investigating the nature of the electronically excited states.

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Publication Details

Journal
The Journal of Physical Chemistry A
Published
2025-06-24
DOI
https://doi.org/10.1021/acs.jpca.5c02982
Citations
1
Primary Topic
Spectroscopy and Quantum Chemical Studies
Type
article
Field-Weighted Citation Impact
1.25

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article

Stabilization Method as a Tool for Electronic State Spectroscopy

M. H. F. Bettega, Pedro A. S. Randi, P. Limão-Vieira
1 citations
The Journal of Physical Chemistry A
Spectroscopy and Quantum Chemical Studies
1.25
article

Stabilization Method as a Tool for Electronic State Spectroscopy

M. H. F. Bettega, Pedro A. S. Randi, P. Limão-Vieira
article en
1 citations

Abstract

We propose a new systematic approach to distinguish valence and diffuse electronically excited states of polyatomic molecules. This method applies the stabilization technique of Hazi and Taylor [<i>Phys. Rev. A</i> <b>1970</b>, 1 (1109)] to neutral excited states, using basis set diffuseness as the stabilization parameter. By monitoring how excited states behave under basis set contraction, one can differentiate valence states from Rydberg and mixed valence-Rydberg states, reducing the arbitrariness of previous strategies. Valence states remain stable, whereas the energies of Rydberg and mixed states vary. This approach is compatible with any electronic structure method. To illustrate its applicability, we characterize the singlet excited states of CCl<sub>4</sub>, HCOOH, and 2-chlorotoluene. This provides a valuable tool for investigating the nature of the electronically excited states.

The Journal of Physical Chemistry AVol. 129(26)
Universidade Federal do Paraná (BR), Universidade Nova de Lisboa (PT)
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Conselho Nacional de Desenvolvimento Científico e Tecnológico, Fundação para a Ciência e a Tecnologia
Affordable and clean energy
Openalex Percentile: Top 20%
Spectroscopy and Quantum Chemical Studies
1.25
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