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arXiv:1702.00957 (physics)

Title:The Elephant in the Room of Density Functional Theory Calculations

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Abstract: Using multiwavelets, we have obtained total energies and corresponding atomization energies for the GGA-PBE and hybrid-PBE0 density functionals for a test set of 211 molecules with an unprecedented and guaranteed $\mu$Hartree accuracy. These quasi-exact references allow us to quantify the accuracy of standard all-electron basis sets that are believed to be highly accurate for molecules, such as Gaussian-type orbitals (GTOs), all-electron numeric atom-centered orbitals (NAOs) and full-potential augmented plane wave (APW) methods. We show that NAOs are able to achieve the so-called chemical accuracy (1 kcal/mol) for the typical basis set sizes used in applications, for both total and atomization energies. For GTOs, a triple-zeta quality basis has mean errors of ~10kcal/mol in total energies, while chemical accuracy is almost reached for a quintuple-zeta basis. Due to systematic error cancellations, atomization energy errors are reduced by almost an order of magnitude, placing chemical accuracy within reach also for medium to large GTO bases, albeit with significant outliers. In order to check the accuracy of the computed densities, we have also investigated the dipole moments, where in general, only the largest NAO and GTO bases are able to yield errors below 0.01 Debye. The observed errors are similar across the different functionals considered here.
Subjects: Computational Physics (physics.comp-ph); Materials Science (cond-mat.mtrl-sci); Chemical Physics (physics.chem-ph)
Journal reference: J. Phys. Chem. Lett., 2017, 8 (7), pp 1449-1457
DOI: 10.1021/acs.jpclett.7b00255
Cite as: arXiv:1702.00957 [physics.comp-ph]
  (or arXiv:1702.00957v1 [physics.comp-ph] for this version)

Submission history

From: José A. Flores-Livas [view email]
[v1] Fri, 3 Feb 2017 10:16:27 UTC (1,773 KB)
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