What Types of Chemical Problems Benefit from Density-Corrected DFT? A Probe Using an Extensive and Chemically Diverse Test Suite.

For the large and chemically diverse GMTKN55 benchmark suite, we have studied the performance of density-corrected density functional theory (HF-DFT), compared to self-consistent DFT, for several pure and hybrid GGA and meta-GGA exchange-correlation (XC) functionals (PBE, BLYP, TPSS, and SCAN) as a function of the percentage of HF exchange in the hybrid. The D4 empirical dispersion correction has been added throughout. For subsets dominated by dynamical correlation, HF-DFT is highly beneficial, particularly at low HF exchange percentages. This is especially true for noncovalent interactions where the electrostatic component is dominant, such as hydrogen and halogen bonds: for π-stacking, HF-DFT is detrimental. For subsets with significant nondynamical correlation (i.e., where a Hartree-Fock determinant is not a good zero-order wavefunction), HF-DFT may do more harm than good. While the self-consistent series show optima at or near 37.5% (i.e., 3/8) for all four XC functionals-consistent with Grimme's proposal of the PBE38 functional-HF-BLYP-D4, HF-PBE-D4, and HF-TPSS-D4 all exhibit minima nearer 25% (i.e., 1/4) as the use of HF orbitals greatly mitigates the error at 25% for barrier heights. Intriguingly, for HF-SCAN-D4, the minimum is near 10%, but the weighted mean absolute error (WTMAD2) for GMTKN55 is only barely lower than that for HF-SCAN-D4 (i.e., where the post-HF step is a pure meta-GGA). The latter becomes an attractive option, only slightly more costly than pure Hartree-Fock, and devoid of adjustable parameters other than the three in the dispersion correction. Moreover, its WTMAD2 is only surpassed by the highly empirical M06-2X and by the combinatorially optimized empirical range-separated hybrids ωB97X-V and ωB97M-V.