Hybrid functional

Hybrid functional

A hybrid functional is an exchange-correlation functional used in density functional theory (DFT) that incorporates a portion of exact exchange from Hartree-Fock theory with exchange and correlation from other sources ("ab initio", such as LDA, or empirical).

Origin

The hybrid approach to density functionals was first introduced by Axel Becke in 1993 [cite journal|author=A.D. Becke|title=A new mixing of Hartree-Fock and local density-functional theories|journal=J. Chem. Phys.|volume=98|pages=1372–1377|year=1993|doi=10.1063/1.464304 ] . Hybridization with Hartree-Fock (exact) exchange provides a simple scheme for improving many molecular properties, such as atomization energies, bond lengths and vibration frequencies, which tend to be poorly described with simple "ab initio" functionals. [cite journal|author=John P. Perdew, Matthias Ernzerhof and Kieron Burke|title=Rationale for mixing exact exchange with density functional approximations|journal=J. Chem. Phys.|volume=105|pages=9982–9985|year=1996|url=http://dft.rutgers.edu/pubs/PEB96.pdf|doi=10.1063/1.472933|unused_data=|access date=2007-05-07]

Method

The exchange-correlation functional for a hybrid is usually a linear combination of the Hartree-Fock exchange (E_x^{ m HF}) and some other one or combination of exchange and correlation functionals. The parameter(s) relating the amount of each functional can be arbitrarily assigned and is usually fitted to reproduce well some set of observables (bond lengths, band gaps, etc.). For example, the popular B3LYP (Becke, three-parameter, Lee-Yang-Parr) [ cite journal | author = K. Kim and K. D. Jordan | title = Comparison of Density Functional and MP2 Calculations on the Water Monomer and Dimer | journal = J. Phys. Chem. | volume = 98 | issue = 40 | pages = 10089–10094 | year = 1994 | doi = 10.1021/j100091a024 ] [ cite journal | author = P.J. Stephens, F. J. Devlin, C. F. Chabalowski and M. J. Frisch | title = "Ab Initio" Calculation of Vibrational Absorption and Circular Dichroism Spectra Using Density Functional Force Fields | journal = J. Phys. Chem. | volume = 98 | pages = 11623–11627 | year = 1994 | doi = 10.1021/j100096a001 ] exchange-correlation functional is:

E_{xc}^{ m B3LYP} = E_{xc}^{ m LDA} + a_0 (E_x^{ m HF} - E_x^{LDA}) + a_x (E_x^{ m GGA} - E_x^{LDA}) + a_c (E_c^{ m GGA} - E_c^{LDA})

where a_0=0.20 ,;, a_x=0.72,;, and a_c=0.81,; are the three empirical parameters; E_x^{GGA} and E_c^{GGA} are the generalized gradient approximation formulated with the Becke 88 exchange functional [cite journal | author = A. D. Becke | title = Density-functional exchange-energy approximation with correct asymptotic behavior | journal = Phys. Rev. A | volume = 38 | pages = 3098–3100 | year = 1988 | url = http://link.aps.org/abstract/PRA/v38/p3098 | doi = 10.1103/PhysRevA.38.3098 ] and the correlation functional of Lee, Yang and Parr [cite journal|author= Chengteh Lee, Weitao Yang and Robert G. Parr|title=Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density|journal=Phys. Rev. B|volume=37|pages=785|year=1988|doi=10.1103/PhysRevB.37.785] , and E_c^{LDA} the VWN correlation functional (see Local-density approximation#Correlation).


=List of hybrid functionals (in Gaussian 03)=

*B3LYP
*B3P86
*B1B95
*B1LYP
*MPW1PW91
*B97
*B98
*B971
*B972
*PBE1PBE
*O3LYP
*BHandH
*BHandHLYP
*BMKSee: cite web|url=http://www.gaussian.com/g_ur/k_dft.htm|title=G03 Manual: DFT

References


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