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Constructing “Full-Frequency” Spectra via Moment Constraints for Coupled Cluster Green’s Functions

[Image: see text] We propose an approach to build “full-frequency” quasiparticle spectra from conservation of a set of static expectation values. These expectation values define the moments of the spectral distribution, resulting in an efficient and systematically improvable expansion. By computing...

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Detalles Bibliográficos
Autores principales: Backhouse, Oliver J., Booth, George H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9648195/
https://www.ncbi.nlm.nih.gov/pubmed/36283078
http://dx.doi.org/10.1021/acs.jctc.2c00670
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author Backhouse, Oliver J.
Booth, George H.
author_facet Backhouse, Oliver J.
Booth, George H.
author_sort Backhouse, Oliver J.
collection PubMed
description [Image: see text] We propose an approach to build “full-frequency” quasiparticle spectra from conservation of a set of static expectation values. These expectation values define the moments of the spectral distribution, resulting in an efficient and systematically improvable expansion. By computing these initial moment constraints at the coupled-cluster level, we demonstrate convergence in both correlated state-specific and full spectral quantities, while requiring a fraction of the effort of traditional Green’s function approaches. Tested across the GW100 benchmark set for charged excitation spectra, we can converge frontier excitations to within the inherent accuracy of the CCSD approximation, while obtaining a simultaneous representation of the entire excitation spectrum at all energy scales.
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spelling pubmed-96481952022-11-15 Constructing “Full-Frequency” Spectra via Moment Constraints for Coupled Cluster Green’s Functions Backhouse, Oliver J. Booth, George H. J Chem Theory Comput [Image: see text] We propose an approach to build “full-frequency” quasiparticle spectra from conservation of a set of static expectation values. These expectation values define the moments of the spectral distribution, resulting in an efficient and systematically improvable expansion. By computing these initial moment constraints at the coupled-cluster level, we demonstrate convergence in both correlated state-specific and full spectral quantities, while requiring a fraction of the effort of traditional Green’s function approaches. Tested across the GW100 benchmark set for charged excitation spectra, we can converge frontier excitations to within the inherent accuracy of the CCSD approximation, while obtaining a simultaneous representation of the entire excitation spectrum at all energy scales. American Chemical Society 2022-10-25 2022-11-08 /pmc/articles/PMC9648195/ /pubmed/36283078 http://dx.doi.org/10.1021/acs.jctc.2c00670 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Backhouse, Oliver J.
Booth, George H.
Constructing “Full-Frequency” Spectra via Moment Constraints for Coupled Cluster Green’s Functions
title Constructing “Full-Frequency” Spectra via Moment Constraints for Coupled Cluster Green’s Functions
title_full Constructing “Full-Frequency” Spectra via Moment Constraints for Coupled Cluster Green’s Functions
title_fullStr Constructing “Full-Frequency” Spectra via Moment Constraints for Coupled Cluster Green’s Functions
title_full_unstemmed Constructing “Full-Frequency” Spectra via Moment Constraints for Coupled Cluster Green’s Functions
title_short Constructing “Full-Frequency” Spectra via Moment Constraints for Coupled Cluster Green’s Functions
title_sort constructing “full-frequency” spectra via moment constraints for coupled cluster green’s functions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9648195/
https://www.ncbi.nlm.nih.gov/pubmed/36283078
http://dx.doi.org/10.1021/acs.jctc.2c00670
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