We develop relativistic short-range exchange energy functionals for four-component relativistic range-separated density-functional theory using a Dirac-Coulomb Hamiltonian in the no-pair approximation. We show how to improve the short-range local-density approximation exchange functional for large range-separation parameters by using the on-top exchange pair density as a new variable. We also develop a relativistic short-range generalized-gradient approximation exchange functional that further increases the accuracy for small range-separation parameters. Tests on the helium, beryllium, neon, and argon isoelectronic series up to high nuclear charges show that the latter functional gives exchange energies with a maximal relative percentage error of 3%. The development of this exchange functional represents a step forward for the application of four-component relativistic range-separated density-functional theory to chemical compounds with heavy elements.
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http://dx.doi.org/10.1063/5.0004926 | DOI Listing |
Philos Trans A Math Phys Eng Sci
July 2024
GSI Helmholtzzentrum für Schwerionenforschung GmbH, Planckstraße 1 , Darmstadt 64291, Germany.
Acc Chem Res
May 2024
CEITEC - Central European Institute of Technology, Masaryk University, Kamenice 5, CZ-625 00 Brno, Czechia.
ConspectusMagnetic resonance techniques represent a fundamental class of spectroscopic methods used in physics, chemistry, biology, and medicine. Electron paramagnetic resonance (EPR) is an extremely powerful technique for characterizing systems with an open-shell electronic nature, whereas nuclear magnetic resonance (NMR) has traditionally been used to investigate diamagnetic (closed-shell) systems. However, these two techniques are tightly connected by the electron-nucleus hyperfine interaction operating in paramagnetic (open-shell) systems.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2023
Faculty of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw, Poland.
The non-additive three-body interaction potential for helium was computed using the coupled-cluster theory and the full configuration interaction method. The obtained potential comprises an improved nonrelativistic Born-Oppenheimer energy and the leading relativistic and nuclear-motion corrections. The mean absolute uncertainty of our calculations due to the incompleteness of the orbital basis set was determined employing complete-basis-set extrapolation techniques and was found to be 1.
View Article and Find Full Text PDFPhys Rev E
May 2023
Department of Physics, University of Oxford, Parks Road, Oxford OX1 3PU, United Kingdom.
The capability for molecular dynamics simulations to treat relativistic dynamics is extended by the inclusion of relativistic kinetic energy. In particular, relativistic corrections to the diffusion coefficient are considered for an argon gas modeled with a Lennard-Jones interaction. Forces are transmitted instantaneously without being retarded, an approximation that is allowed due to the short-range nature of the Lennard-Jones interaction.
View Article and Find Full Text PDFSci Rep
November 2022
Center for Relativistic Laser Science, Institute for Basic Science, Gwangju, 61005, Korea.
We describe an approach to the description of the time-development of the process of strong field ionization of atoms based on the calculation of the joint probability of occurrence of two events, event B being finding atom in the ionized state after the end of the laser pulse, event A being finding a particular value of a given physical observable at a moment of time inside the laser pulse duration. As an example of such an physical observable we consider lateral velocity component of the electron's velocity. Our approach allows us to study time-evolution of the lateral velocity distribution for the ionized electron during the interval of the laser pulse duration.
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