Reduced explicitly correlated Hartree-Fock approach within the nuclear-electronic orbital framework: Theoretical formulation

被引:30
作者
Sirjoosingh, Andrew [1 ]
Pak, Michael V. [1 ]
Swalina, Chet [1 ]
Hammes-Schiffer, Sharon [1 ]
机构
[1] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
基金
加拿大自然科学与工程研究理事会; 美国国家科学基金会;
关键词
NON-BORN-OPPENHEIMER; PLESSET MP2-R12 CALCULATIONS; DENSITY-FUNCTIONAL THEORY; WAVE-FUNCTIONS; GAUSSIAN FUNCTIONS; PERTURBATION-THEORY; CORRELATION CUSP; ALTERNATIVE FORMULATION; PROTON CORRELATION; GENERAL-THEORY;
D O I
10.1063/1.4812257
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 nuclear-electronic orbital (NEO) method treats electrons and select nuclei quantum mechanically on the same level to extend beyond the Born-Oppenheimer approximation. Electron-nucleus dynamical correlation has been found to be highly significant due to the attractive Coulomb interaction. The explicitly correlated Hartree-Fock (NEO-XCHF) approach includes explicit electron-nucleus correlation with Gaussian-type geminal functions during the variational optimization of the nuclear-electronic wavefunction. Although accurate for small model systems, the NEO-XCHF method is computationally impractical for larger chemical systems. In this paper, we develop the reduced explicitly correlated Hartree-Fock approach, denoted NEO-RXCHF, where only select electronic orbitals are explicitly correlated to the nuclear orbitals. By explicitly correlating only the relevant electronic orbitals to the nuclear orbitals, the NEO-RXCHF approach avoids problems that can arise when all electronic orbitals are explicitly correlated to the nuclear orbitals in the same manner. We examine three different NEO-RXCHF methods that differ in the treatment of the exchange between the geminal-coupled electronic orbitals and the other electronic orbitals: NEO-RXCHF-fe is fully anti-symmetric with respect to exchange of all electronic coordinates and includes all electronic exchange terms; NEO-RXCHF-ne neglects the exchange between the geminal-coupled electronic orbitals and the other electronic orbitals; and NEO-RXCHF-ae includes approximate exchange terms between the geminal-coupled electronic orbitals and the other electronic orbitals. The latter two NEO-RXCHF methods offer substantial computational savings over the NEO-XCHF approach. The NEO-RXCHF approach is applicable to a wide range of chemical systems that exhibit non-Born-Oppenheimer effects between electrons and nuclei, as well as positron-containing molecular systems. (C) 2013 AIP Publishing LLC.
引用
收藏
页数:16
相关论文
共 57 条
[1]   The electron and nuclear orbitals model: current challenges and future prospects [J].
Bochevarov, AD ;
Valeev, EF ;
Sherrill, CD .
MOLECULAR PHYSICS, 2004, 102 (01) :111-123
[2]   THE INTEGRAL FORMULAE FOR THE VARIATIONAL SOLUTION OF THE MOLECULAR MANY-ELECTRON WAVE EQUATION IN TERMS OF GAUSSIAN FUNCTIONS WITH DIRECT ELECTRONIC CORRELATION [J].
BOYS, SF .
PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES A-MATHEMATICAL AND PHYSICAL SCIENCES, 1960, 258 (1294) :402-411
[3]   Born-Oppenheimer and Non-Born-Oppenheimer, Atomic and Molecular Calculations with Explicitly Correlated Gaussians [J].
Bubin, Sergiy ;
Pavanelo, Michele ;
Tung, Wei-Cheng ;
Sharkey, Keeper L. ;
Adamowicz, Ludwik .
CHEMICAL REVIEWS, 2013, 113 (01) :36-79
[4]   Non-Born-Oppenheimer calculations of atoms and molecules [J].
Cafiero, M ;
Bubin, S ;
Adamowicz, L .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2003, 5 (08) :1491-1501
[5]   MANY-ELECTRON EXPLICITLY CORRELATED GAUSSIAN FUNCTIONS .1. GENERAL-THEORY AND TEST-RESULTS [J].
CENCEK, W ;
RYCHLEWSKI, J .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (02) :1252-1261
[6]   BENCHMARK CALCULATIONS FOR 2-ELECTRON SYSTEMS USING EXPLICITLY CORRELATED GAUSSIAN FUNCTIONS [J].
CENCEK, W ;
KOMASA, J ;
RYCHLEWSKI, J .
CHEMICAL PHYSICS LETTERS, 1995, 246 (4-5) :417-420
[7]   HYDROGEN TUNNELING IN ENZYME-REACTIONS [J].
CHA, Y ;
MURRAY, CJ ;
KLINMAN, JP .
SCIENCE, 1989, 243 (4896) :1325-1330
[8]   Development of Electron-Proton Density Functionals for Multicomponent Density Functional Theory [J].
Chakraborty, Arindam ;
Pak, Michael V. ;
Hammes-Schiffer, Sharon .
PHYSICAL REVIEW LETTERS, 2008, 101 (15)
[9]   Inclusion of explicit electron-proton correlation in the nuclear-electronic orbital approach using Gaussian-type geminal functions [J].
Chakraborty, Arindam ;
Pak, Michael V. ;
Hammes-Schiffer, Sharon .
JOURNAL OF CHEMICAL PHYSICS, 2008, 129 (01)
[10]   Toward the multi-component quantum theory of atoms in molecules: a variational derivation [J].
Goli, Mohammad ;
Shahbazian, Shant .
THEORETICAL CHEMISTRY ACCOUNTS, 2013, 132 (06) :1-17