Improving the accuracy of the variational quantum eigensolver for molecular systems by the explicitly-correlated perturbative [2]R12-correction

  • We provide an integration of the universal, perturbative explicitly correlated [2]R12-correction in the context of the Variational Quantum Eigensolver (VQE). This approach is able to increase the accuracy of the underlying reference method significantly while requiring no additional quantum resources. The proposed approach only requires knowledge of the one- and two-particle reduced density matrices (RDMs) of the reference wavefunction; these can be measured after having reached convergence in the VQE. This computation comes at a cost that scales as the sixth power of the number of electrons. We explore the performance of the VQE + [2]R12 approach using both conventional Gaussian basis sets and our recently proposed directly determined pair-natural orbitals obtained by multiresolution analysis (MRA-PNOs). Both Gaussian orbital and PNOs are investigated as a potential set of complementary basis functions in the computation of [2]R12. In particular the combination of MRA-PNOs with [2]R12We provide an integration of the universal, perturbative explicitly correlated [2]R12-correction in the context of the Variational Quantum Eigensolver (VQE). This approach is able to increase the accuracy of the underlying reference method significantly while requiring no additional quantum resources. The proposed approach only requires knowledge of the one- and two-particle reduced density matrices (RDMs) of the reference wavefunction; these can be measured after having reached convergence in the VQE. This computation comes at a cost that scales as the sixth power of the number of electrons. We explore the performance of the VQE + [2]R12 approach using both conventional Gaussian basis sets and our recently proposed directly determined pair-natural orbitals obtained by multiresolution analysis (MRA-PNOs). Both Gaussian orbital and PNOs are investigated as a potential set of complementary basis functions in the computation of [2]R12. In particular the combination of MRA-PNOs with [2]R12 has turned out to be very promising – persistently throughout our data, this allowed very accurate simulations at a quantum cost of a minimal basis set. Additionally, we found that the deployment of PNOs as complementary basis can greatly reduce the number of complementary basis functions that enter the computation of the correction at a complexity.show moreshow less

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Metadaten
Author:Philipp Schleich, Jakob S. KottmannORCiDGND, Alán Aspuru-Guzik
Frontdoor URLhttps://opus.bibliothek.uni-augsburg.de/opus4/102010
ISSN:1463-9076OPAC
ISSN:1463-9084OPAC
Parent Title (English):Physical Chemistry Chemical Physics
Publisher:Royal Society of Chemistry (RSC)
Place of publication:Cambridge
Type:Article
Language:English
Year of first Publication:2022
Release Date:2023/02/14
Tag:Physical and Theoretical Chemistry; General Physics and Astronomy
Volume:24
Issue:22
First Page:13550
Last Page:13564
DOI:https://doi.org/10.1039/d2cp00247g
Institutes:Fakultät für Angewandte Informatik
Fakultät für Angewandte Informatik / Institut für Informatik
Fakultät für Angewandte Informatik / Institut für Informatik / Professur für Quantenalgorithmik