Category:Exchange-correlation functionals: Difference between revisions

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U_{\rm H}[\rho] = \int v_{\rm ext}({\bf r})\rho({\bf r})d^{3}r
U_{\rm H}[\rho] = \int v_{\rm ext}({\bf r})\rho({\bf r})d^{3}r
</math>
</math>
 
:<math>
\hat{V}_{\rm nn} = \sum_{A=1}^{M-1}\sum_{B=A+1}^{M}
\frac{e^{2}}{4\pi\epsilon_{0}}
\frac{Z_{A}Z_{B}}{\left\vert{\bf R}_{A}-{\bf R}_{B}\right\vert}
</math>
== Theoretical Background ==
== Theoretical Background ==
*Hybrid functionals: {{TAG|Hartree-Fock and HF/DFT hybrid functionals}}.
*Hybrid functionals: {{TAG|Hartree-Fock and HF/DFT hybrid functionals}}.

Revision as of 10:37, 18 January 2022

In Kohn-Sham density functional theory (DFT)[1][2], the total energy is given by

where is the non-interacting kinetic energy of the electrons, the Hartree energy, the third term is the energy of the electrons-nuclei attraction interaction, and is the nuclei-nuclei repulsion energy.

Theoretical Background

How to


Subcategories

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Pages in category "Exchange-correlation functionals"

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