Combining the spin-separated exact two-component relativistic Hamiltonian with the equation-of-motion coupled-cluster method for the treatment of spin-orbit splittings of light and heavy elements

被引:46
作者
Cao, Zhanli [1 ]
Li, Zhendong [2 ,3 ]
Wang, Fan [1 ]
Liu, Wenjian [2 ,3 ]
机构
[1] Sichuan Univ, Inst Atom & Mol Phys, Key Lab High Energy Dens Phys & Technol, Minist Educ, Chengdu, Peoples R China
[2] Peking Univ, State Key Lab Rare Earth Mat Chem & Applicat, Inst Theoret & Computat Chem, Beijing Natl Lab Mol Sci,Coll Chem & Mol Engn, Beijing 100871, Peoples R China
[3] Peking Univ, Ctr Computat Sci & Engn, Beijing 100871, Peoples R China
关键词
ANO BASIS-SETS; CONFIGURATION-INTERACTION; PROGRAM PACKAGE; SHELL SYSTEMS; STATES; BDF;
D O I
10.1039/c6cp07588f
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
The spin-separated exact two-component (X2C) relativistic Hamiltonian [sf-X2C+ so-DKHn, J. Chem. Phys., 2012, 137, 154114] is combined with the equation-of-motion coupled-cluster method with singles and doubles (EOM-CCSD) for the treatment of spin-orbit splittings of open-shell molecular systems. Scalar relativistic effects are treated to infinite order from the outset via the spin-free part of the X2C Hamiltonian (sf-X2C), whereas the spin-orbit couplings (SOC) are handled at the CC level via the first-order Douglas-Kroll-Hess (DKH) type of spin-orbit operator (so-DKH1). Since the exponential of single excitations, i.e., exp(T-1), introduces sufficient spin orbital relaxations, the inclusion of SOC at the CC level is essentially the same in accuracy as the inclusion of SOC from the outset in terms of the two-component spinors determined variationally by the sf-X2C+ so-DKH1 Hamiltonian, but is computationally more efficient. Therefore, such an approach (denoted as sf-X2C-EOM-CCSD(SOC)) can achieve uniform accuracy for the spin-orbit splittings of both light and heavy elements. For light elements, the treatment of SOC can even be postponed until the EOM step (denoted as sf-X2C-EOM(SOC)-CCSD), so as to further reduce the computational cost. To reveal the efficacy of sf-X2C-EOM-CCSD(SOC) and sf-X2C-EOM(SOC)-CCSD, the spin-orbit splittings of the (2)Pi states of monohydrides up to the sixth row of the periodic table are investigated. The results show that sf-X2C-EOM-CCSD(SOC) predicts very accurate results (within 5%) for elements up to the fifth row, whereas sf-X2C-EOM(SOC)-CCSD is useful only for light elements (up to the third row but with some exceptions). For comparison, the sf-X2C-S-TD-DFT-SOC approach [spin-adapted open-shell time-dependent density functional theory, Mol. Phys., 2013, 111, 3741] is applied to the same systems. The overall accuracy (1-10%) is satisfactory.
引用
收藏
页码:3713 / 3721
页数:9
相关论文
共 71 条
[1]  
[Anonymous], 2008, J CHEM PHYS
[2]  
[Anonymous], 2014, J CHEM PHYS
[3]  
[Anonymous], 2010, J CHEM PHYS
[4]  
[Anonymous], 1988, J PHYS CHEM
[5]  
[Anonymous], 1979, CONSTANTS DIATOMIC M
[6]   EFFECTS OF THE MAGNETIC PART OF THE BREIT TERM ON THE (2)PI STATES OF DIATOMIC HYDRIDES [J].
BAECK, KK ;
LEE, YS .
JOURNAL OF CHEMICAL PHYSICS, 1994, 100 (04) :2888-2895
[7]   Coupled-cluster theory in quantum chemistry [J].
Bartlett, Rodney J. ;
Musial, Monika .
REVIEWS OF MODERN PHYSICS, 2007, 79 (01) :291-352
[8]   DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) :5648-5652
[9]   DENSITY-FUNCTIONAL EXCHANGE-ENERGY APPROXIMATION WITH CORRECT ASYMPTOTIC-BEHAVIOR [J].
BECKE, AD .
PHYSICAL REVIEW A, 1988, 38 (06) :3098-3100
[10]   Spin-orbit matrix elements for internally contracted multireference configuration interaction wavefunctions [J].
Berning, A ;
Schweizer, M ;
Werner, HJ ;
Knowles, PJ ;
Palmieri, P .
MOLECULAR PHYSICS, 2000, 98 (21) :1823-1833