Premium
Large basis sets and geometry optimizations in embedded cluster calculations
Author(s) -
Teunissen E. H.,
Jansen A. P. J.
Publication year - 1995
Publication title -
international journal of quantum chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.484
H-Index - 105
eISSN - 1097-461X
pISSN - 0020-7608
DOI - 10.1002/qua.560540110
Subject(s) - basis set , cluster (spacecraft) , basis (linear algebra) , adsorption , chemistry , crystal (programming language) , geometry , basis function , boundary (topology) , set (abstract data type) , crystallography , molecular physics , computational chemistry , mathematics , mathematical analysis , computer science , density functional theory , programming language
In the embedded cluster method, a cluster is embedded in a correction potential. This potential adds the long‐range electrostatic forces of the crystal and subtracts the electrostatic potential of the boundary errors of the cluster. The correction potential is calculated from the wave function of the cluster and the crystal. So far, the method has only been used on a cluster having the same geometry and basis set as that of the crystal. Here, we calculated the adsorption energies of NH 3 and NH 4 + on an embedded zeolite cluster with different basis sets and modified geometries. We showed that a mixed basis set, a basis set having a large basis set on the atoms around the adsorption site and a minimal basis set on the atoms of the boundary of the cluster, yields adsorption energies close to that of the large basis set. The optimized geometries of the zeolite acidic site were almost equal for the nonembedded cluster, the embedded cluster, and the crystal. By combining the mixed basis set with a partial geometry optimization, an improved description of the adsorption process is obtained. © 1995 John Wiley & Sons, Inc.