1. Density functional investigations of the properties and thermochemistry of UF6 and UF5 using valence-electron and all-electron approaches
- Author
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Gustavo E. Scuseria, Richard L. Martin, Juan E. Peralta, P. Jeffrey Hay, and Enrique R. Batista
- Subjects
Chemistry ,General Physics and Astronomy ,Electron ,Bond-dissociation energy ,Hybrid functional ,symbols.namesake ,Chemical thermodynamics ,Thermochemistry ,symbols ,Density functional theory ,Physical and Theoretical Chemistry ,Atomic physics ,Hamiltonian (quantum mechanics) ,Valence electron - Abstract
The structural properties and thermochemistry of UF6 and UF5 have been investigated using both Hartree-Fock and density functional theory (DFT) approximations. Within the latter approach, the local spin-density approximation, the generalized gradient approximation, and hybrid density functionals were considered. To describe the uranium atom we employed small-core (60 electrons) and large-core (78 electrons) relativistic effective core potentials (RECPs), as well as the all-electron approximation based on the two-component third-order Douglas-Kroll-Hess Hamiltonian. For structural properties, we obtained very good agreement with experiment with DFT and both large and small-core RECPs. The best match with experiment is given by the hybrid functionals with the small-core RECP. The bond dissociation energy (BDE) was obtained from the relative energies of the fragments [UF6 --> UF5 + F], corrected for zero-point energy and spin-orbit interaction. Very good agreement was found between the BDE obtained from all-electron calculations and those calculated with the small-core RECP, while those from the large-core RECP are off by more than 50%. In order to obtain good agreement with experiment in the BDE it is imperative to work with hybrid density functionals and a small-core RECP.
- Published
- 2004