The Journal of Physical Chemistry A · 2019 · 479 citations · 121 references
Natural SciencesChemistryPhysicsComputational ChemistryDrug DesignMolecular PhysicsAb Initio MethodsChemical Space ExplorationDensity Functional TheoryMolecular Orbital TheoryDispersion CorrectionsHybrid FunctionalTotal Energy Functionals
with the size of the system. Dependence of WTMAD2 for DSD functionals on the percentage of HF exchange is roughly quadratic; it is sufficiently weak that any reasonable value in the 64% to 72% range can be chosen semiarbitrarily. DSD-SCAN and DOD-SCAN double hybrids involving the SCAN nonempirical meta-GGA as the semilocal component have also been considered and offer a good alternative if one wishes to eliminate either the empirical dispersion correction or the same-spin correlation component. noDispSD-SCAN66 achieves WTMAD2 = 3.0 kcal/mol, compared to 2.7 kcal/mol for DOD-SCAN66-D4. However, the best performance without dispersion corrections (WTMAD2 = 2.8 kcal/mol) is reached by revωB97X-2, a slight reparametrization of the Chai-Head-Gordon range-separated double hybrid. Finally, in the context of double-hybrid functionals, the very recent D4 dispersion correction is clearly superior over D3(BJ).
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Generalized Gradient Approximation Made Simple
John P. Perdew, Kieron Burke, Matthias Ernzerhof · Physical Review Letters · 1996 · 211.5K citations · Full text
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Density-functional thermochemistry. III. The role of exact exchange
Axel D. Becke · The Journal of Chemical Physics · 1993 · 102.8K citations
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