A FRAGMENT MULTIPOLE APPROACH TO LONG-RANGE COULOMB INTERACTIONS IN HARTREE-FOCK CALCULATIONS ON LARGE SYSTEMS
Artikel i vetenskaplig tidskrift, 1992

An efficient ab initio method for electronic structure calculations on extended molecular systems is presented, along with some illustrative applications. A division of the system into subunits allows the interactions to be separated into short- and long-range contributions, leading to a reduction of the computational effort from the original fourth-power size-dependence to one that is approximately quadratic. The short-range contributions to the Fock matrix are obtained in an essentially conventional fashion, while the long-range interactions are evaluated using a two-center multipole expansion formalism. The number of short-range contributions grows only linearly with the number of subunits, while the long-range contributions grow as N2. Systematic studies of the computational efforts for systems of up to 99 water molecules organized as one-stranded chains, three-stranded chains, and three-dimensional clusters, as well as alkane chains with up to 69 carbon atoms, have been performed. In these model systems, the overall computational effort grows as N(K) where 1 < K < 2.

Författare

Itai Panas

Chalmers, Institutionen för oorganisk miljökemi

Jan Almlöf

International Journal of Quantum Chemistry

0020-7608 (ISSN) 1097-461X (eISSN)

Vol. 43 1073-1089

Ämneskategorier

Teoretisk kemi

DOI

10.1002/qua.560420438