The generality of the GUGA MRCI approach in COLUMBUS for treating complex quantum chemistry

0524012 - ÚOCHB 2021 RIV US eng J - Článek v odborném periodiku
Lischka, H. - Shepard, R. - Müller, T. - Szalay, P. G. - Pitzer, R. M. - Aquino, A. J. A. - do Nascimento, M. M. A. - Barbatti, M. - Belcher, L. T. - Blaudeau, J. P. - Borges, I. - Brozell, S. R. - Carter, E. A. - Das, A. - Gidofalvi, G. - González, L. - Hase, W. L. - Kedziora, G. - Kertesz, M. - Kossoski, F. - Machado, F. B. C. - Matsika, S. - do Monte, S. A. - Nachtigallová, Dana - Nieman, R. - Oppel, M. - Parish, C. A. - Plasser, F. - Spada, R. F. K. - Stahlberg, E. A. - Ventura, E. - Yarkony, D. R. - Zhang, Z.
The generality of the GUGA MRCI approach in COLUMBUS for treating complex quantum chemistry.
Journal of Chemical Physics. Roč. 152, č. 13 (2020), č. článku 134110. ISSN 0021-9606. E-ISSN 1089-7690
Grant CEP: GA ČR(CZ) GA18-09914S
Institucionální podpora: RVO:61388963
Klíčová slova: Gaussian basis sets * correlated molecular calculations * size-extensive modification
Obor OECD: Physical chemistry
Impakt faktor: 3.488, rok: 2020
Způsob publikování: Omezený přístup
https://aip.scitation.org/doi/10.1063/1.5144267

The core part of the program system COLUMBUS allows highly efficient calculations using variational multireference (MR) methods in the framework of configuration interaction with single and double excitations (MR-CISD) and averaged quadratic coupled-cluster calculations (MR-AQCC), based on uncontracted sets of configurations and the graphical unitary group approach (GUGA). The availability of analytic MR-CISD and MR-AQCC energy gradients and analytic nonadiabatic couplings for MR-CISD enables exciting applications including, e.g., investigations of pi-conjugated biradicaloid compounds, calculations of multitudes of excited states, development of diabatization procedures, and furnishing the electronic structure information for on-the-fly surface nonadiabatic dynamics. With fully variational uncontracted spin-orbit MRCI, COLUMBUS provides a unique possibility of performing high-level calculations on compounds containing heavy atoms up to lanthanides and actinides. Crucial for carrying out all of these calculations effectively is the availability of an efficient parallel code for the CI step. Configuration spaces of several billion in size now can be treated quite routinely on standard parallel computer clusters. Emerging developments in COLUMBUS, including the all configuration mean energy multiconfiguration self-consistent field method and the graphically contracted function method, promise to allow practically unlimited configuration space dimensions. Spin density based on the GUGA approach, analytic spin-orbit energy gradients, possibilities for local electron correlation MR calculations, development of general interfaces for nonadiabatic dynamics, and MRCI linear vibronic coupling models conclude this overview.
Trvalý link: http://hdl.handle.net/11104/0308333