Third-Order Møller-Plesset Perturbation Theory Made Useful? Choice of Orbitals and Scaling Greatly Improves Accuracy for Thermochemistry, Kinetics, and Intermolecular Interactions.

Autor: Bertels LW; Department of Chemistry , University of California , Berkeley , California 94720 , United States., Lee J; Department of Chemistry , University of California , Berkeley , California 94720 , United States., Head-Gordon M; Department of Chemistry , University of California , Berkeley , California 94720 , United States.; Chemical Sciences Division , Lawrence Berkeley National Laboratory , Berkeley , California 94720 , United States.
Jazyk: angličtina
Zdroj: The journal of physical chemistry letters [J Phys Chem Lett] 2019 Aug 01; Vol. 10 (15), pp. 4170-4176. Date of Electronic Publication: 2019 Jul 12.
DOI: 10.1021/acs.jpclett.9b01641
Abstrakt: We develop and test methods that include second- and third-order perturbation theory (MP3) using orbitals obtained from regularized orbital-optimized second-order perturbation theory, κ-OOMP2, denoted as MP3:κ-OOMP2. Testing MP3:κ-OOMP2 shows RMS errors that are 1.7-5 times smaller than those of MP3 across 7 data sets. To do still better, empirical training of the scaling factors for the second- and third-order correlation energies and the regularization parameter on one of those data sets led to an unregularized scaled ( c 2 = 1.0; c 3 = 0.8) denoted as MP2.8:κ-OOMP2. MP2.8:κ-OOMP2 yields significant additional improvement over MP3:κ-OOMP2 in 4 of 6 test data sets on thermochemistry, kinetics, and noncovalent interactions. Remarkably, these two methods outperform coupled cluster with singles and doubles in 5 of the 7 data sets considered, at greatly reduced cost (no O ( N 6 ) iterations).
Databáze: MEDLINE