Explicitly Correlated Double-Hybrid DFT: A Comprehensive Analysis of the Basis Set Convergence on the GMTKN55 Database

Abstract

Double-hybrid density functional theory (DHDFT) offers a pathway to accuracy approaching composite wavefunction approaches such as G4 theory. However, the Görling-Levy second-order perturbation theory (GLPT2) term causes them to partially inherit the slow ∝L^-3 (with L the maximum angular momentum) basis set convergence of correlated wavefunction methods. This could potentially be remedied by introducing F12 explicit correlation: we investigate the basis set convergence of both DHDFT and DHDFT-F12 (where GLPT2 is replaced by GLPT2-F12) for the large and chemically diverse general main-group thermochemistry, kinetics, and noncovalent interactions (GMTKN55) benchmark suite. The B2GP-PLYP-D3(BJ) and revDSD-PBEP86-D4 DHDFs are investigated as test cases, together with orbital basis sets as large as aug-cc-pV5Z and F12 basis sets as large as cc-pVQZ-F12. We show that F12 greatly accelerates basis set convergence of DHDFs, to the point that even the modest cc-pVDZ-F12 basis set is closer to the basis set limit than cc-pV(Q+d)Z or def2-QZVPPD in orbital-based approaches, and in fact comparable in quality to cc-pV(5+d)Z. Somewhat surprisingly, aug-cc-pVDZ-F12 is not required even for the anionic subsets. In conclusion, DHDF-F12/VDZ-F12 eliminates concerns about basis set convergence in both the development and applications of double-hybrid functionals. Mass storage and I/O bottlenecks for larger systems can be circumvented by localized pair natural orbital approximations, which also exhibit much gentler system size scaling.

Figure 1

Sensitivity analysis of the B2GP-PLYP-F12-D3(BJ)/V{D,T}Z extrapolation.Root-mean-square deviation (rmsd) differences [rmsd(extrapolation exponent α—rmsd(∞)] for the atomization energies of the W4-11 set calculated relative to B2GP-PLYP-F12-D3(BJ)/V{T,Q}Z-F12.