Alternative Representations of the Correlation Energy in Density-Functional Theory: A Kinetic-Energy Based Adiabatic Connection

被引:8
|
作者
Teale, Andrew M. [1 ,2 ]
Helgaker, Trygve [2 ]
Savin, Andreas [3 ,4 ]
机构
[1] Univ Nottingham, Sch Chem, Univ Pk, Nottingham NG7 2RD, England
[2] Univ Oslo, Dept Chem, Ctr Theoret & Computat Chem, POB 1033 Blindern, N-0315 Oslo, Norway
[3] Univ Paris 06, Sorbonne Univ, Chim Theor Lab, UMR 7616, F-75005 Paris, France
[4] CNRS, UMR 7616, Chim Theor Lab, F-75005 Paris, France
基金
欧洲研究理事会;
关键词
Density-functional theory; Adiabatic connection; Correlation energy; Coupled-cluster theory; Kohn-Sham theory; STRONG-INTERACTION LIMIT; BASIS-SETS; ATOMS; EXCHANGE;
D O I
10.1002/jccs.201500132
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The adiabatic-connection framework has been widely used to explore the properties of the correlation energy in density-functional theory. The integrand in this formula may be expressed in terms of the electron-electron interactions directly, involving intrinsically two-particle expectation values. Alternatively, it may be expressed in terms of the kinetic energy, involving only one-particle quantities. In this work, we explore this alternative representation for the correlation energy and highlight some of its potential for the construction of new density functional approximations. The kinetic-energy based integrand is effective in concentrating static correlation effects to the low interaction strength regime and approaches zero asymptotically, offering interesting new possibilities for modeling the correlation energy in density-functional theory
引用
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页码:121 / 128
页数:8
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