<scp>SC</scp> Cellular multiple scattering in molecular electronic structure calculations

Abstract

Abstract Recent advances in the statistical exchange approximation to the one‐electron potential and in the use of general potentials in multiple scattering are studied numerically and combined in a cellular multiple scattering calculation of the electronic structure of molecules. The particular examples of these calculations are SF 6 , H , and H 2 , the results being compared with those of previous approximations and other techniques. It is first seen that the X αβ approximation or a similar one based on the use of a universal parametrization of the statistical exchange (and some effects of correlation) part of the potential will provide the maximum of freedom in the partition of the real space of the molecules into cells. This avoids arbitrariness in the assumed value of the parameters to be used in every cell. The usefulness of the X αβ approximation in a muffin‐tin and in a cellular calculation is discussed. It is also found that the usual limitation to muffin‐tin‐like potentials, while simpler as a first approximation, can be removed without unduly increasing the computing effort. However, an accurate evaluation of the real self‐consistent potential in each cell (or even in a muffin‐tin) will increase the length of the program, the storage necessities and the computing time by a factor estimated to be between three and ten according to the geometry considered. It is concluded that the cellular multiple scattering method offers the best possibilities for a systematic use of multiple scattering techniques in molecular calculations.