@article{zhou_kincaid_wang_annaberdiyev_ganesh_mitas_2024, title={A new generation of effective core potentials: Selected lanthanides and heavy elements}, volume={160}, ISSN={["1089-7690"]}, DOI={10.1063/5.0180057}, abstractNote={We construct correlation-consistent effective core potentials (ccECPs) for a selected set of heavy atoms and f elements that are currently of significant interest in materials and chemical applications, including Y, Zr, Nb, Rh, Ta, Re, Pt, Gd, and Tb. As is customary, ccECPs consist of spin–orbit (SO) averaged relativistic effective potential (AREP) and effective SO terms. For the AREP part, our constructions are carried out within a relativistic coupled-cluster framework while also taking into account objective function one-particle characteristics for improved convergence in optimizations. The transferability is adjusted using binding curves of hydride and oxide molecules. We address the difficulties encountered with f elements, such as the presence of large cores and multiple near-degeneracies of excited levels. For these elements, we construct ccECPs with core–valence partitioning that includes 4f subshell in the valence space. The developed ccECPs achieve an excellent balance between accuracy, size of the valence space, and transferability and are also suitable to be used in plane wave codes with reasonable energy cutoffs.}, number={8}, journal={JOURNAL OF CHEMICAL PHYSICS}, author={Zhou, Haihan and Kincaid, Benjamin and Wang, Guangming and Annaberdiyev, Abdulgani and Ganesh, Panchapakesan and Mitas, Lubos}, year={2024}, month={Feb} }
 @article{wang_kincaid_zhou_annaberdiyev_bennett_krogel_mitas_2022, title={A new generation of effective core potentials from correlated and spin-orbit calculations: Selected heavy elements}, volume={157}, ISSN={["1089-7690"]}, DOI={10.1063/5.0087300}, abstractNote={We introduce new correlation consistent effective core potentials (ccECPs) for the elements I, Te, Bi, Ag, Au, Pd, Ir, Mo, and W with 4d, 5d, 6s, and 6p valence spaces. These ccECPs are given as a sum of spin-orbit averaged relativistic effective potential (AREP) and effective spin–orbit (SO) terms. The construction involves several steps with increasing refinements from more simple to fully correlated methods. The optimizations are carried out with objective functions that include weighted many-body atomic spectra, norm-conservation criteria, and SO splittings. Transferability tests involve molecular binding curves of corresponding hydride and oxide dimers. The constructed ccECPs are systematically better and in a few cases on par with previous effective core potential (ECP) tables on all tested criteria and provide a significant increase in accuracy for valence-only calculations with these elements. Our study confirms the importance of the AREP part in determining the overall quality of the ECP even in the presence of sizable spin–orbit effects. The subsequent quantum Monte Carlo calculations point out the importance of accurate trial wave functions that, in some cases (mid-series transition elements), require treatment well beyond a single-reference.}, number={5}, journal={JOURNAL OF CHEMICAL PHYSICS}, author={Wang, Guangming and Kincaid, Benjamin and Zhou, Haihan and Annaberdiyev, Abdulgani and Bennett, M. Chandler and Krogel, Jaron T. and Mitas, Lubos}, year={2022}, month={Aug} }
 @article{zhou_scemama_wang_annaberdiyev_kincaid_caffarel_mitas_2022, title={A quantum Monte Carlo study of systems with effective core potentials and node nonlinearities}, volume={554}, ISSN={["1873-4421"]}, DOI={10.1016/j.chemphys.2021.111402}, abstractNote={We study beryllium dihydride (BeH2) and acetylene (C2H2) molecules using real-space diffusion Monte Carlo (DMC) method. The molecules serve as perhaps the simplest prototypes that illustrate the difficulties with biases in the fixed-node DMC calculations that might appear with the use of effective core potentials (ECPs) or other nonlocal operators. This is especially relevant for the recently introduced correlation consistent ECPs (ccECPs) for 2s2p elements. Corresponding ccECPs exhibit deeper potential functions due to higher fidelity to all-electron counterparts, which could lead to larger local energy fluctuations. We point out that the difficulties stem from issues that are straightforward to address by upgrades of basis sets, use of T-moves for nonlocal terms, inclusion of a few configurations into the trial function and similar. The resulting accuracy corresponds to the ccECP target (chemical accuracy) and it is in consistent agreement with independent correlated calculations. Further possibilities for upgrading the reliability of the DMC algorithm and considerations for better adapted and more robust Jastrow factors are discussed as well.}, journal={CHEMICAL PHYSICS}, author={Zhou, Haihan and Scemama, Anthony and Wang, Guangming and Annaberdiyev, Abdulgani and Kincaid, Benjamin and Caffarel, Michel and Mitas, Lubos}, year={2022}, month={Feb} }
 @article{kincaid_wang_zhou_mitas_2022, title={Correlation consistent effective core potentials for late 3d transition metals adapted for plane wave calculations}, volume={157}, ISSN={["1089-7690"]}, DOI={10.1063/5.0109098}, abstractNote={We construct a new modification of correlation consistent effective core potentials (ccECPs) for late 3d elements Cr–Zn with Ne-core that are adapted for efficiency and low energy cut-offs in plane wave calculations. The decrease in accuracy is rather minor, so that the constructions are in the same overall accuracy class as the original ccECPs. The resulting new constructions work with energy cut-offs at or below ≈400 Ry and, thus, make calculations of large systems with transition metals feasible for plane wave codes. We also provide the basic benchmarks for atomic spectra and molecular tests of this modified option that we denote as ccECP-soft.}, number={17}, journal={JOURNAL OF CHEMICAL PHYSICS}, author={Kincaid, Benjamin and Wang, Guangming and Zhou, Haihan and Mitas, Lubos}, year={2022}, month={Nov} }