Hybrid functionals

go back to Main Page, Group Pages, Núria López and Group

This page is under edition, it may not make sense yet :) (feel free to ask, if you have questions)

Hybrid functional theory

tbd

Implementation

VASP

• For all hybrid functional calculations, set:

 LHFCALC = .TRUE.

• For HSE calculations, set the HFSCREEN parameter:

 HFSCREEN = 0.2 # HSE06
 HFSCREEN = 0.3 # HSE03

The HFSCREEN parameter specifies the distance (in 1/Å) at which the exact (Hartree-Fock) exchange is screened. Therefore HF exact exchange is screened at a distance larger than 5 Å (HSE06), or 3.333 Å (HSE03), respectively, the way it is implemented in VASP. The difference between HSE03 and HSE06 is discussed in detail by Krukau et al. J. Chem. Phys. 125, 224106 (2006): https://aip.scitation.org/doi/abs/10.1063/1.2404663

• Defining the amount of introduced exact exchange:

 AEXX  = 0.25   # Amount of exact HF exchange, ie. 25%
 AGGAX = 0.75   # Amount of GGA exchange, i.e. 75 %

This is the default setting with 25 % exact exchange, you may reduce that number, in particular if you have compounds with transition metals and/or degenerate electronic states (see theory above).

• HSE03-13: This functional was optimised to fit the band gap of CoFe Prussian blue compounds; it generally presents a good compromise for calculating ionic solid compounds, which contain coordinated transition metal centres

 LHFCALC = .TRUE.
 HFSCREEN = 0.3 # HSE03
 AEXX  = 0.13   # Amount of exact HF exchange, ie. 13%
 AGGAX = 0.87   # Amount of GGA exchange, i.e. 87 %

There are of course many other hybrid functionals, which require different settings, but generally they can be described by defining the GGA functional and the above-listed parameters.

(see also: https://cms.mpi.univie.ac.at/wiki/index.php/Specific_hybrid_functionals)

Quantum Espresso

(...)