Van der Waals interactions studied by density functional theory

Abstract

A new density functional theory (DFT) for calculations of van der Waals (vdW) complexes is presented. In this scheme, a long-range-corrected exchange-correlation functional is combined with a new damping method of the Andersson–Langreth–Lundqvist (ALL) vdW correlation functional for dealing with molecules containing various types of atoms. The long-range correction (LC) scheme for the exchange functional was used in this method. This LC-DFT+ALL method was applied to calculations of rare-gas dimers and vdW complexes, consisting of diatomic molecules and He atoms. The present method reproduces very accurate potential energy surfaces of these systems. In particular, for CO–He complexes, LC-DFT+ALL gives an equilibrium bending structure in agreement with experiment without using a particular basis function, while the collinear structure is given by conventional DFT and high-level ab initio molecular orbital methods without using a bond function. By comparing LC-DFT and ALL component energies, it was found that LC plays a major role in the determination of vdW complex structures. This LC-DFT+ALL method has proved to be a powerful tool for quantitative calculations of large weakly bound systems because it requires much less computational time than high-level ab initio methods.

Acknowledgements

Sincere thanks to Professor Nicholas C. Handy for his longstanding encouragement. This research was supported by a Grant-in-Aid for Scientific Research on a Priority Area (A) from the Japanese Ministry of Education, Science, Sports, and Culture and by a grant from the Genesis Research Institute, Inc.

Notes

This paper is dedicated to Professor Nicholas C. Handy.

Additional information

Notes on contributors

K. Hirao *

This paper is dedicated to Professor Nicholas C. Handy.