S66x8 noncovalent interactions revisited: new benchmark and performance of composite localized coupled-cluster methods. Issue 41 (18th October 2022)
- Record Type:
- Journal Article
- Title:
- S66x8 noncovalent interactions revisited: new benchmark and performance of composite localized coupled-cluster methods. Issue 41 (18th October 2022)
- Main Title:
- S66x8 noncovalent interactions revisited: new benchmark and performance of composite localized coupled-cluster methods
- Authors:
- Santra, Golokesh
Semidalas, Emmanouil
Mehta, Nisha
Karton, Amir
Martin, Jan M. L. - Abstract:
- Abstract : The S66x8 noncovalent interactions benchmark has been re-evaluated at the "sterling silver" level. Against this, a selection of computationally more economical alternatives has been assayed, ranging from localized CC to double hybrids and SAPT(DFT). Abstract : The S66x8 noncovalent interactions benchmark has been re-evaluated at the "sterling silver" level, using explicitly correlated MP2-F12 near the complete basis set limit, CCSD(F12*)/aug-cc-pVTZ-F12, and a (T) correction from conventional CCSD(T)/sano-V{D, T}Z+ calculations. The revised reference values differ by 0.1 kcal mol −1 RMS from the original Hobza benchmark and its revision by Brauer et al., but by only 0.04 kcal mol −1 RMS from the "bronze" level data in Kesharwani et al., Aust. J. Chem., 2018, 71, 238–248. We then used these to assess the performance of localized-orbital coupled cluster approaches with and without counterpoise corrections, such as PNO-LCCSD(T) as implemented in MOLPRO, DLPNO-CCSD(T1 ) as implemented in ORCA, and LNO-CCSD(T) as implemented in MRCC, for their respective "Normal", "Tight", and "very Tight" settings. We also considered composite approaches combining different basis sets and cutoffs. Furthermore, in order to isolate basis set convergence from domain truncation error, for the aug-cc-pVTZ basis set we compared PNO, DLPNO, and LNO approaches with canonical CCSD(T). We conclude that LNO-CCSD(T) with veryTight criteria performs very well for "raw" (CP-uncorrected), butAbstract : The S66x8 noncovalent interactions benchmark has been re-evaluated at the "sterling silver" level. Against this, a selection of computationally more economical alternatives has been assayed, ranging from localized CC to double hybrids and SAPT(DFT). Abstract : The S66x8 noncovalent interactions benchmark has been re-evaluated at the "sterling silver" level, using explicitly correlated MP2-F12 near the complete basis set limit, CCSD(F12*)/aug-cc-pVTZ-F12, and a (T) correction from conventional CCSD(T)/sano-V{D, T}Z+ calculations. The revised reference values differ by 0.1 kcal mol −1 RMS from the original Hobza benchmark and its revision by Brauer et al., but by only 0.04 kcal mol −1 RMS from the "bronze" level data in Kesharwani et al., Aust. J. Chem., 2018, 71, 238–248. We then used these to assess the performance of localized-orbital coupled cluster approaches with and without counterpoise corrections, such as PNO-LCCSD(T) as implemented in MOLPRO, DLPNO-CCSD(T1 ) as implemented in ORCA, and LNO-CCSD(T) as implemented in MRCC, for their respective "Normal", "Tight", and "very Tight" settings. We also considered composite approaches combining different basis sets and cutoffs. Furthermore, in order to isolate basis set convergence from domain truncation error, for the aug-cc-pVTZ basis set we compared PNO, DLPNO, and LNO approaches with canonical CCSD(T). We conclude that LNO-CCSD(T) with veryTight criteria performs very well for "raw" (CP-uncorrected), but struggles to reproduce counterpoise-corrected numbers even for veryveryTight criteria: this means that accurate results can be obtained using either extrapolation from basis sets large enough to quench basis set superposition error (BSSE) such as aug-cc-pV{Q, 5}Z, or using a composite scheme such as Tight{T, Q} + 1.11[vvTight(T) − Tight(T)]. In contrast, PNO-LCCSD(T) works best with counterpoise, while performance with and without counterpoise is comparable for DLPNO-CCSD(T1 ). Among more economical methods, the highest accuracies are seen for dRPA75-D3BJ, ωB97M-V, ωB97M(2), revDSD-PBEP86-D4, and DFT(SAPT) with a TDEXX or ATDEXX kernel. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 24:Issue 41(2022)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 24:Issue 41(2022)
- Issue Display:
- Volume 24, Issue 41 (2022)
- Year:
- 2022
- Volume:
- 24
- Issue:
- 41
- Issue Sort Value:
- 2022-0024-0041-0000
- Page Start:
- 25555
- Page End:
- 25570
- Publication Date:
- 2022-10-18
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d2cp03938a ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 24223.xml