Automatic Differentiation for Explicitly Correlated MP2

Automatic differentiation (AD) offers a route to achieve arbitrary-order derivatives of challenging wave function methods without the use of analytic gradients or response theory. Currently, AD has been predominantly used in methods where first- and/or second-order derivatives are available, but it has not been applied to methods lacking available derivatives. The most robust approximation of explicitly correlated MP2, MP2-F12/3C(FIX)+CABS, is one such method. By comparing the results of MP2-F12 computed with AD versus finite-differences, it is shown that (a) optimized geometries match to about 10<sup>-3</sup> Å for bond lengths and a 10<sup>-6</sup> degree for angles, and (b) dipole moments match to about 10<sup>-6</sup> D. Hessians were observed to have poorer agreement with numerical results (10<sup>-5</sup>), which is attributed to deficiencies in AD implementations currently. However, it is notable that vibrational frequencies match within 10<sup>-2</sup> cm<sup>-1</sup>. The use of AD also allowed the prediction of MP2-F12/3C(FIX)+CABS IR intensities for the first time.

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Publication Details

Journal
Journal of Chemical Theory and Computation
Published
2024-09-23
DOI
https://doi.org/10.1021/acs.jctc.4c00818
Citations
3
Primary Topic
Spectroscopy and Quantum Chemical Studies
Type
article
Field-Weighted Citation Impact
1.01

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article

Automatic Differentiation for Explicitly Correlated MP2

Erica C. Mitchell, Henry F. Schaefer, Justin M. Turney
3 citations
Journal of Chemical Theory and Computation
Spectroscopy and Quantum Chemical Studies
1.01
article

Automatic Differentiation for Explicitly Correlated MP2

Erica C. Mitchell, Henry F. Schaefer, Justin M. Turney
article en
3 citations

Abstract

Automatic differentiation (AD) offers a route to achieve arbitrary-order derivatives of challenging wave function methods without the use of analytic gradients or response theory. Currently, AD has been predominantly used in methods where first- and/or second-order derivatives are available, but it has not been applied to methods lacking available derivatives. The most robust approximation of explicitly correlated MP2, MP2-F12/3C(FIX)+CABS, is one such method. By comparing the results of MP2-F12 computed with AD versus finite-differences, it is shown that (a) optimized geometries match to about 10<sup>-3</sup> Å for bond lengths and a 10<sup>-6</sup> degree for angles, and (b) dipole moments match to about 10<sup>-6</sup> D. Hessians were observed to have poorer agreement with numerical results (10<sup>-5</sup>), which is attributed to deficiencies in AD implementations currently. However, it is notable that vibrational frequencies match within 10<sup>-2</sup> cm<sup>-1</sup>. The use of AD also allowed the prediction of MP2-F12/3C(FIX)+CABS IR intensities for the first time.

Journal of Chemical Theory and ComputationVol. 20(19)
University of Georgia (US)
Basic Energy Sciences
Openalex Percentile: Top 24%
Spectroscopy and Quantum Chemical Studies
1.01
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Automatic Differentiation for Explicitly Correlated MP2 — Erica C. Mitchell, Henry F. Schaefer, et al. · Journal of Chemical Theory and Computation (2024) | TGRS Research Map | TGRS