Pseudopotential density functional treament of atoms and molecules in cartesian coordinate grid

Abstract

This is a follow-up of our recently proposed work on pseudopotential calculation (Ref. [21]) of atoms and molecules within DFT framework, using cartesian coordinate grid. Detailed results are presented to demonstrate the usefulness, applicability of the same for a larger set of species (5 atoms; 53 molecules) and exchange-correlation functionals (local, nonlocal). A thorough comparison on total, component, ionization, atomization energies, eigenvalues, potential energy curves with available literature data shows excellent agreement. Additionally, HOMO energies for a series of molecules show significant improvements by using the Leeuwen-Baerends exchange potential, compared to other functionals considered. Comparison with experiments has been made, wherever possible.

19 pages, 2 figures,

References in corpus (2)

• Real-Space Mesh Techniques in Density Functional Theory
• Grid-based density functional calculation of many-electron systems

Cited by in corpus (2)

• Efficient HF exchange evaluation through Fourier convolution in Cartesian grid for orbital-dependent density functionals
• A self-consistent systematic optimization of range-separated hybrid functionals from first principles