Communication: Rationale for a new class of double-hybrid approximations in density-functional theory

被引:93
作者
Toulouse, Julien [1 ,2 ]
Sharkas, Kamal [1 ,2 ,3 ]
Bremond, Eric [4 ]
Adamo, Carlo [2 ]
机构
[1] Univ Paris 06, Chim Theor Lab, F-75005 Paris, France
[2] CNRS, F-75005 Paris, France
[3] Atom Energy Commiss Syria, Damascus, Syria
[4] Chim ParisTech, Lab Electrochim Chim Interfaces & Modelisat Energ, F-75005 Paris, France
关键词
CORRELATED MOLECULAR CALCULATIONS; GAUSSIAN-BASIS SETS; THERMOCHEMICAL KINETICS; CORRELATION-ENERGY;
D O I
10.1063/1.3640019
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We provide a rationale for a new class of double-hybrid approximations introduced by Bremond and Adamo [J. Chem. Phys. 135, 024106 (2011)] which combine an exchange-correlation density functional with Hartree-Fock exchange weighted by lambda and second-order Moller-Plesset (MP2) correlation weighted by lambda(3). We show that this double-hybrid model can be understood in the context of the density-scaled double-hybrid model proposed by Sharkas et al. [J. Chem. Phys. 134, 064113 (2011)], as approximating the density-scaled correlation functional E(c)[n(1/lambda)] by a linear function of lambda, interpolating between MP2 at lambda = 0 and a density-functional approximation at lambda = 1. Numerical results obtained with the Perdew-Burke-Ernzerhof density functional confirms the relevance of this double-hybrid model. (C) 2011 American Institute of Physics. [doi:10.1063/1.3640019]
引用
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页数:3
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