An atom-in-molecule adaptive polarized valence single-ζ atomic orbital basis for electronic structure calculations.

Many low-cost or semiempirical quantum mechanical-based electronic structure methods suffer from the use of unpolarized minimal atomic orbital (AO) basis sets. In this work, we overcome this limitation by a fully DFT variationally optimized, adaptive minimal basis set consistently available for the elements up to radon (Z = 86). The new key feature is to make the linear coefficients of the primitive Gaussians in a contracted AO dependent on the effective atomic charge of the atom in the molecule, i.e., each symmetry-unique atom obtains its "own" specifically adapted basis functions. In this way, the physically important "breathing" of the AOs in a molecule with (a) atomic charge (expansion/contraction for anionic/cationic states) and (b) the number of close-lying bonded neighbor atoms is accounted for. The required atomic charges are obtained from a specially developed extended Hückel type Hamiltonian and the coordination numbers from the molecule geometry. Proper analytical derivatives of the resulting adaptive basis functions can easily be derived. Moreover, the basis functions are electric field-dependent, thus improving the description of, e.g., dipole moments and polarizabilities. The new basis set termed q-vSZP (charge dependent valence single-ζ, polarized) is thoroughly benchmarked for atomic/molecular and thermochemical properties compared to standard minimal and double-ζ basis sets at the DFT level with the accurate ωB97X-D4 functional. It is shown that q-vSZP is clearly superior to existing minimal basis sets, often reaching double-ζ quality or even better results. We expect it to be the optimal choice in future semiempirical quantum mechanical methods. [ABSTRACT FROM AUTHOR]