On the accuracy of density functionals and their basis set dependence: An extensive study on the main group homonuclear diatomic molecules Li2 to Br2
✍ Scribed by Roland H. Hertwig; Wolfram Koch
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 943 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0192-8651
No coin nor oath required. For personal study only.
✦ Synopsis
The equilibrium bond distances, harmonic frequencies, and bond dissociation energies of the 21 homonuclear diatomics Li,-F,, Na,-Cl,, and K,-Br, have been determined using approximate density functional theory (DFT) employing various widely used functionals and basis sets ranging from single zeta to triple zeta plus polarization quality. The results are in general much less sensitive to the size of the basis set as in conventional ab initio molecular orbital (MO) theory, while the choice of the functional is of much more significance. For one basis set (6-311G*), the performance of the DFT-based calculations has been compared and found to be superior to Hartree-Fock (HF) Mdler Plesset second order perturbation theory (MP2), or configuration interaction with single and double excitations (CISD) calculations. Particularly, no pathological cases, such as the group 2 dimers (Be,, Mg,, Ca,), are observed. 0 1995 by John Wiley & Sons, Inc.
tional ab initio methods for the calculation of molecular properties like binding energies, equilibrium geometries, or harmonic frequencies has increased dramatically over the last decade.',' It is not the aim of this article to review developments in density functional theory, but to introduce the terminology and to enable the reader to place the remainder Of this article into a broader context, we