Scalable Electron Correlation Methods. 8. Explicitly Correlated Open-Shell Coupled-Cluster with Pair Natural Orbitals...

We present explicitly correlated open-shell pair natural orbital local coupled-cluster methods, PNO-RCCSD(T)-F12 and PNO-UCCSD(T)-F12. The methods are extensions of our previously reported PNO-R/UCCSD methods (J. Chem. Theory Comput., 2020, 16, 3135-3151, https://pubs.acs.org/doi/10.1021/acs.jctc.0c00192) with additions of explicit correlation and perturbative triples corrections. The explicit correlation treatment follows the spin-orbital CCSD-F12b theory using Ansatz 3*A, which is found to yield comparable or better basis set convergence than the more rigorous Ansatz 3C in computed ionization potentials and reaction energies using double- to quaduple-ζ basis sets. The perturbative triples correction is adapted from the spin-orbital (T) theory to use triples natural orbitals (TNOs). To address the coupling due to off-diagonal Fock matrix elements, the local triples amplitudes are iteratively solved using small domains of TNOs, and a semicanonical (T0) domain correction with larger domains is applied to reduce the domain errors. The performance of the methods is demonstrated through benchmark calculations on ionization potentials, radical stabilization energies, reaction energies of fragmentations and rearrangements in radical cations, and spin-state energy differences of iron complexes. For a few test sets where canonical calculations are feasible, PNO-RCCSD(T)-F12 results agree with the canonical ones to within 0.4 kcal mol^-1, and this maximum error is reduced to below 0.2 kcal mol^-1 when large local domains are used. For larger systems, results using different thresholds for the local approximations are compared to demonstrate that 1 kcal mol^-1 level of accuracy can be achieved using our default settings. For a couple of difficult cases, it is demonstrated that the errors from individual approximations are only a fraction of 1 kcal mol^-1, and the overall accuracy of the method does not rely on error compensations. In contrast to canonical calculations, the use of spin-orbitals does not lead to a significant increase of computational time and memory usage in the most expensive steps of PNO-R/UCCSD(T)-F12 calculations. The only exception is the iterative solution of the (T) amplitudes, which can be avoided without significant errors by using a perturbative treatment of the off-diagonal coupling, known as (T1) approximation. For most systems, even the semicanonical approximation (T0) leads only to small errors in relative energies. Our program is well parallelized and capable of computing accurate correlation energies for molecules with 100-200 atoms using augmented triple-ζ basis sets in less than a day of elapsed time on a small computer cluster.