An additive reference correction scheme for the transcorrelated method
We introduce an additive reference correction for the transcorrelated (TC) method and its three-body mean-field approximation (xTC) to improve energy differences computed in small orbital basis sets. The correction is motivated by the observation that, for xTC atomization energies, the dominant error in double-ζ bases originates from the reference contribution rather than from the correlation energy. In the proposed reference-corrected scheme (RC-xTC), the small-basis correlation energy is retained, while the corresponding TC reference energy is replaced by its value from a larger basis. Benchmark calculations for the non-relativistic HEAT set with the Dunning basis-set family show that RC-xTC substantially improves both total and atomization energies relative to standard xTC in double-ζ bases. At the CCSD(T) level, RC-xTC yields better atomization energies than CCSD(T)-F12a in the double-ζ regime, while preserving the favorable total-energy accuracy of xTC. At the CCSD level, RC-xTC improves atomization energies relative to F12a throughout the full basis-set sequence. As the basis set is enlarged, xTC and RC-xTC become progressively identical, as expected from the construction of the correction.
Authors
- Daniel Kats (ORCID: https://orcid.org/0000-0002-7274-0601)
- Kristoffer Simula (ORCID: https://orcid.org/0000-0002-6714-8427)
- Evelin Martine Corvid Christlmaier (ORCID: https://orcid.org/0000-0001-9193-8982)
- Ali Alavi (ORCID: https://orcid.org/0000-0002-0654-9489)
- Johannes Hauskrecht
- Yifan Cheng
Institutions
- University of Cambridge (GB)
- Max Planck Institute for Solid State Research (DE)
Publication Details
- Journal
- The Journal of Chemical Physics
- Published
- 2026-09-22
- DOI
- https://doi.org/10.1063/5.0349731
- Primary Topic
- Advanced Chemical Physics Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00