The Nonlocal Kernel in van der Waals Density Functionals as an Additive Correction: An Extensive Analysis with...

The development of van der Waals density functional approximations (vdW-DFAs) has gained considerable interest over the past decade. While in a strictest sense, energy calculations with vdW-DFAs should be carried out fully self-consistently, we demonstrate conclusively for a total of 11 methods that such a strategy only increases the computational time effort without having any significant effect on energetic properties, electron densities, or orbital-energy differences. The strategy to apply a nonlocal vdW-DFA kernel as an additive correction to a fully converged conventional DFA result is therefore justified and more efficient. As part of our study, we utilize the extensive GMTKN55 database for general main-group thermochemistry, kinetics, and noncovalent interactions [ Phys. Chem. Chem. Phys. 2017, 19, 32184], which allows us to analyze the very promising B97M-V [ J. Chem. Phys. 2015, 142, 074111] and ωB97M-V [ J. Chem. Phys. 2016, 144, 214110] DFAs. We also present new DFT-D3(BJ) based counterparts of these two methods and of ωB97X-V [ J. Chem. Theory Comput 2013, 9, 263], which are faster variants with similar accuracy. Our study concludes with updated recommendations for the general method user, based on our current overview of 325 dispersion-corrected and -uncorrected DFA variants analyzed for GMTKN55. vdW-DFAs are the best representatives of the three highest rungs of Jacob's Ladder, namely, B97M-V, ωB97M-V, and DSD-PBEP86-NL.