Seniority number in spin-adapted spaces and compactness of configuration interaction wave functions

被引:40
作者
Alcoba, Diego R. [1 ,2 ]
Torre, Alicia [3 ]
Lain, Luis [3 ]
Massaccesi, Gustavo E. [4 ]
Ona, Ofelia B. [5 ]
机构
[1] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Fis, RA-1428 Buenos Aires, DF, Argentina
[2] Consejo Nacl Invest Cient & Tecn, Inst Fis Buenos Aires, RA-1428 Buenos Aires, DF, Argentina
[3] Univ Basque Country, Fac Ciencia & Tecnol, Dept Quim Fis, E-48080 Bilbao, Spain
[4] Univ Buenos Aires, Dept Ciencias Exactas, Ciclo Basico Comun, RA-1428 Buenos Aires, DF, Argentina
[5] Univ Nacl La Plata, Consejo Nacl Invest Cient & Tecn, CCT La Plata, Inst Invest Fis Quim Teor & Aplicadas, RA-1900 La Plata, Buenos Aires, Argentina
关键词
ORDER REPLACEMENT OPERATORS; DENSITY-MATRIX; UNPAIRED ELECTRONS; AB-INITIO; LOCALIZATION; TRACES; DECOMPOSITION;
D O I
10.1063/1.4818755
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
This work extends the concept of seniority number, which has been widely used for classifying N-electron Slater determinants, to wave functions of N electrons and spin S, as well as to N-electron spin-adapted Hilbert spaces. We propose a spin-free formulation of the seniority number operator and perform a study on the behavior of the expectation values of this operator under transformations of the molecular basis sets. This study leads to propose a quantitative evaluation for the convergence of the expansions of the wave functions in terms of Slater determinants. The non-invariant character of the seniority number operator expectation value of a wave function with respect to a unitary transformation of the molecular orbital basis set, allows us to search for a change of basis which minimizes that expectation value. The results found in the description of wave functions of selected atoms and molecules show that the expansions expressed in these bases exhibit a more rapid convergence than those formulated in the canonical molecular orbital bases and even in the natural orbital ones. (C) 2013 AIP Publishing LLC.
引用
收藏
页数:6
相关论文
共 52 条
[1]   On the measure of electron correlation and entanglement in quantum chemistry based on the cumulant of the second-order reduced density matrix [J].
Alcoba, D. R. ;
Bochicchio, R. C. ;
Lain, L. ;
Torre, A. .
JOURNAL OF CHEMICAL PHYSICS, 2010, 133 (14)
[2]   On the definition of the effectively unpaired electron density matrix: A similarity measure approach [J].
Alcoba, Diego R. ;
Bochicchio, Roberto C. ;
Lain, Luis ;
Torre, Alicia .
CHEMICAL PHYSICS LETTERS, 2006, 429 (1-3) :286-288
[3]   An orbital localization criterion based on the theory of "fuzzy" atoms [J].
Alcoba, DR ;
Lain, L ;
Torre, A ;
Bochicchio, RC .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 2006, 27 (05) :596-608
[4]   Unitarily invariant decomposition of arbitrary hermitian matrices of physical interest [J].
Alcoba, DR .
INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, 2004, 97 (03) :776-783
[5]   Split-localized orbitals can yield stronger configuration interaction convergence than natural orbitals [J].
Bytautas, L ;
Ivanic, J ;
Ruedenberg, K .
JOURNAL OF CHEMICAL PHYSICS, 2003, 119 (16) :8217-8224
[6]   Seniority and orbital symmetry as tools for establishing a full configuration interaction hierarchy [J].
Bytautas, Laimutis ;
Henderson, Thomas M. ;
Jimenez-Hoyos, Carlos A. ;
Ellis, Jason K. ;
Scuseria, Gustavo E. .
JOURNAL OF CHEMICAL PHYSICS, 2011, 135 (04)
[7]   Electron collisions with the BeH+ molecular ion in the R-matrix approach [J].
Chakrabarti, K. ;
Tennyson, J. .
EUROPEAN PHYSICAL JOURNAL D, 2012, 66 (01)
[8]  
CIOSLOWSKI J, 1990, INT J QUANTUM CHEM, P15
[9]   DOUBLY-OCCUPIED ORBITAL MCSCF METHODS .1. PEMCSCF METHOD - FORMULATION AND APPLICATION TO SMALL MOLECULES [J].
COOK, DB .
MOLECULAR PHYSICS, 1975, 30 (03) :733-743
[10]   Generalized molecular orbital theory .2. [J].
Couty, M ;
Hall, MB .
JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (37) :6936-6944