学术文献库

Density functional theory (DFT) is used in thousands of papers each year, yet lack of universality reduces DFT's predictive capacity, and functionals may produce energy-density imbalances. The absolute electronegativity (χ) and hardness (η) directly reflect the energy-density relationship via the chemical potential dE/dN and we thus hypothesized that they probe universality. We studied χand ηfor atoms Z = 1-36 using 50 diverse functionals covering all major classes. Very few functionals describe both χand ηwell. ηbenefits from error cancelation whereas χis marred by error propagation from IP and EA; thus almost all standard GGA and hybrid functionals display a plateau in the MAE at 0.2-0.3 eV for η. In contrast, variable performance for χindicates problems in describing the chemical potential by DFT. The accuracy and precision of a functional is far from linearly related, yet for a universal functional we expect linearity. Popular functionals such as B3LYP, PBE, and revPBE, perform poorly for both properties. Density sensitivity calculations indicate large density-derived errors as occupation of degenerate p- and d-orbitals causes "non-universality" and large dependency on exact exchange. Thus, we argue that performance for χfor the same systems is a hallmark of universality by probing dE/dN. With this metric, B98, B97-1, PW6B95D3, APFD are the most "universal" tested functionals. B98 and B97-1 are accurate for very diverse metal-ligand bonds, supporting that a balanced description of dE/dN and dE2/dN2, via χand η, is probably a first simple probe of universality.