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

This is a follow-up of our recently proposed work on pseudopotential calculation [A.K. Roy, Int. J. Quant. Chem. 108 (2008) 837] 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.