Main Page
About Science
Faculty Deanship
Letter of Dean
Overview of Deanship
Vice Deans
Vice Dean
Letter of Vice-dean
Overview of Vice-deanship
Vice Dean for Graduate Studies
Letter of Vice Dean for Graduate Studies
Overview of Vice Dean of Postgraduate Studies
Research and Innovation Unit
Vice Dean for Girls Campus
Faculty Management
Letter of Managing Director-Boys Campus
Letter of Managing Director-Girls Campus
Overview of Management
Educational Affairs
Males Campus
Staff
Females Campus
Contact Us
Research
عربي
English
About
Admission
Academic
Research and Innovations
University Life
E-Services
Search
Faculty of Sciences
Document Details
Document Type
:
Article In Journal
Document Title
:
On the formulation of a density matrix functional for Van der Waals interaction of like- and opposite-spin electrons in the helium dimer
On the formulation of a density matrix functional for Van der Waals interaction of like- and opposite-spin electrons in the helium dimer
Document Language
:
English
Abstract
:
Whereas a density functional that incorporates dispersion interaction has remained elusive to date, we demonstrate that in principle the dispersion energy can be obtained from a density matrix functional. In density matrix functional theory one tries to find suitable approximations to the two-particle reduced density matrix (2RDM) in terms of natural orbitals (NOs) and natural orbital occupation numbers (ONs). The total energy is then given as a function(al) of the NOs and ONs, i.e., as an implicit functional of the 1RDM. The left-right correlation in a (dissociating) bond, as well as various types of dynamical correlation, can be described accurately with a NO functional employing only J and K integrals (JK-only functional). We give a detailed analysis of the full CI wavefunction of the He-2 dimer, from which the dispersion part of the two-particle density matrix is obtained. It emerges that the entirely different physics embodied in the dispersion interaction leads to an essentially different type of exchange-correlation orbital functional for the dispersion energy (non-JK). The distinct NO functionals for the different types of correlation imply that they can be used in conjunction without problems of double counting. Requirements on the (primitive) basis set for Van der Waals bonding appear to be more modest than for other types of correlation
ISSN
:
0021-9606
Journal Name
:
JOURNAL OF CHEMICAL PHYSICS
Volume
:
137
Issue Number
:
20
Publishing Year
:
1433 AH
2012 AD
Article Type
:
Article
Added Date
:
Wednesday, July 12, 2017
Researchers
Researcher Name (Arabic)
Researcher Name (English)
Researcher Type
Dr Grade
Email
l Mentel
Mentel, l
Researcher
x Sheng
Sheng, x
Researcher
o Gritsenko
Gritsenko, o
Researcher
e Baerends
Baerends, e
Researcher
Files
File Name
Type
Description
42073.pdf
pdf
Back To Researches Page