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.
Authors
- Erica C. Mitchell (ORCID: https://orcid.org/0000-0001-5649-5776)
- Henry F. Schaefer (ORCID: https://orcid.org/0000-0003-0252-2083)
- Justin M. Turney (ORCID: https://orcid.org/0000-0003-3659-0711)
Institutions
- University of Georgia (US)
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
Funders
- Basic Energy Sciences