Natural Orbitals for Wave Function Based Correlated Calculations Using a Plane Wave Basis Set

Author(s)
Andreas Grüneis, George H. Booth, Martijn Marsman, James Spencer, Ali Alavi, Georg Kresse
Abstract

We demonstrate that natural orbitals allow for reducing the computational cost of wave function based correlated calculations, especially for atoms and molecules in a large box, when a plane wave basis set under periodic boundary conditions is used. The employed natural orbitals are evaluated on the level of second-order Moller-Plesset perturbation theory (MP2), which requires a computational effort that scales as O(N(5)), where N is a measure of the system size. Moreover, we find that a simple approximation reducing the scaling to O(N(4)) yields orbitals that allow for a similar reduction of the number of virtual orbitals. The MP2 natural orbitals are applied to coupled-cluster singles and doubles (CCSD) as well as full configuration interaction Quantum Monte Carlo calculations of the H(2) molecule to test our implementation. Finally, the atomization energies of the LiH molecule and solid are calculated on the level of MP2 and CCSD.

Organisation(s)
Computational Materials Physics
External organisation(s)
University of Cambridge, Imperial College London
Journal
Journal of Chemical Theory and Computation
Volume
7
Pages
2780-2785
No. of pages
6
ISSN
1549-9618
DOI
https://doi.org/10.1021/ct200263g
Publication date
2011
Peer reviewed
Yes
Austrian Fields of Science 2012
103009 Solid state physics, 103025 Quantum mechanics, 103018 Materials physics, 104022 Theoretical chemistry
Portal url
https://ucrisportal.univie.ac.at/en/publications/8053ba41-e949-4142-9c1b-6d4efa8ec5e5