Challenges for Density Functional Theory

被引:1958
作者
Cohen, Aron J. [1 ]
Mori-Sanchez, Paula
Yang, Weitao
机构
[1] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
基金
美国国家科学基金会;
关键词
EXCHANGE-CORRELATION ENERGY; GENERALIZED GRADIENT APPROXIMATION; SELF-INTERACTION ERROR; FULL CONFIGURATION-INTERACTION; FRACTIONAL PARTICLE NUMBER; MAIN-GROUP THERMOCHEMISTRY; DER-WAALS INTERACTIONS; AB-INITIO CALCULATION; KOHN-SHAM POTENTIALS; ADIABATIC CONNECTION;
D O I
10.1021/cr200107z
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Understanding current and future challenges for density functional theory (DFT) are focused. One of the main challenges for DFT is to keep as its cornerstone some element of simplicity. It also include the need to improve the description of reaction barriers and dispersion/van der waals interactions and understand the energy of two protons separated by infinity with one and two electrons. It is very difficult to determine an accurate form of the exchangecorrelation from first principles. A more practical approach is to take available experimental information to help determine and test the functional forms. It is important to address the particularly challenging problem of exchangecorrelation from other angles as well such as constructing approximate functionals and minimizing the total energy. The essence of self-interaction can be understood from the behavior of the energy of one electron.
引用
收藏
页码:289 / 320
页数:32
相关论文
共 299 条
[1]   Toward reliable density functional methods without adjustable parameters: The PBE0 model [J].
Adamo, C ;
Barone, V .
JOURNAL OF CHEMICAL PHYSICS, 1999, 110 (13) :6158-6170
[2]   Chemistry without Coulomb tails [J].
Adamson, RD ;
Dombroski, JP ;
Gill, PMW .
CHEMICAL PHYSICS LETTERS, 1996, 254 (5-6) :329-336
[3]   Helium dimer dispersion forces and correlation potentials in density functional theory [J].
Allen, MJ ;
Tozer, DJ .
JOURNAL OF CHEMICAL PHYSICS, 2002, 117 (24) :11113-11120
[4]   Zn coordination chemistry: Development of benchmark suites for geometries, dipole moments, and bond dissociation energies and their use to test and validate density functionals and molecular orbital theory [J].
Amin, Elizabeth A. ;
Truhlar, Donald G. .
JOURNAL OF CHEMICAL THEORY AND COMPUTATION, 2008, 4 (01) :75-85
[5]   van der Waals interactions in density-functional theory [J].
Andersson, Y ;
Langreth, DC ;
Lundqvist, BI .
PHYSICAL REVIEW LETTERS, 1996, 76 (01) :102-105
[6]   Infrared spectra and density functional theory calculations on transition metal nitrosyls. Vibrational frequencies of unsaturated transition metal nitrosyls [J].
Andrews, L ;
Citra, A .
CHEMICAL REVIEWS, 2002, 102 (04) :885-911
[7]   Local hybrid exchange-correlation functionals based on the dimensionless density gradient [J].
Arbuznikov, Alexei V. ;
Kaupp, Martin .
CHEMICAL PHYSICS LETTERS, 2007, 440 (1-3) :160-168
[8]   What can we learn from the adiabatic connection formalism about local hybrid functionals? [J].
Arbuznikov, Alexei V. ;
Kaupp, Martin .
JOURNAL OF CHEMICAL PHYSICS, 2008, 128 (21)
[9]   The dependence on and continuity of the energy and other molecular properties with respect to the number of electrons [J].
Ayers, Paul W. .
JOURNAL OF MATHEMATICAL CHEMISTRY, 2008, 43 (01) :285-303
[10]   Gaussian-3 theory using density functional geometries and zero-point energies [J].
Baboul, AG ;
Curtiss, LA ;
Redfern, PC ;
Raghavachari, K .
JOURNAL OF CHEMICAL PHYSICS, 1999, 110 (16) :7650-7657