skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Benchmark Calculations on the Electron Detachment Energies of MO₃⁻ and M₂O₆⁻ (M = Cr, Mo, W)

Journal Article · · Journal of Physical Chemistry A, 111(46):11908-11921
DOI:https://doi.org/10.1021/jp074768i· OSTI ID:959217

The research described in this product was performed in part in the Environmental Molecular Sciences Laboratory, a national scientific user facility sponsored by the Department of Energy's Office of Biological and Environmental Research and located at Pacific Northwest National Laboratory. Neutral and anionic molecules of the monomers and dimers of the group VIB transition metal oxides (MO₃ and M₂O₆) were studied with density functional theory (DFT) and coupled cluster CCSD(T) theory. Franck- Condon simulations of the photoelectron spectra were carried out for the transition from the ground state of the anion to that of the neutral molecule. Molecular structures from the DFT and CCSD(T) methods are compared. Electron detachment energies reported in the literature were evaluated. The calculated adiabatic and vertical electron detachment energies (ADEs and VDEs) were compared with the experimental results. CCSD(T) gives results within 0.12 eV for the ADEs. CCSD(T) predicts VDEs that are in error by as much as 0.3 eV for M = Cr. DFT hybrid functionals were found to give poor results for the ADEs and VDEs for M = Cr due to the substantial amount of multireference character in the wavefunction, whereas the pure DFT functionals give superior results. For M = Mo and W, excellent agreement was found for both CCSD(T) and many DFT fucntionals. The BP86 functional yields the best overall results for the VDEs of all the metal oxide clusters considered. Heats of formation calculated at the CCSD(T) level extrapolated to the complete basis set limit are also in good agreement with available experimental data.

Research Organization:
Pacific Northwest National Lab. (PNNL), Richland, WA (United States). Environmental Molecular Sciences Lab. (EMSL)
Sponsoring Organization:
USDOE
DOE Contract Number:
AC05-76RL01830
OSTI ID:
959217
Journal Information:
Journal of Physical Chemistry A, 111(46):11908-11921, Vol. 111, Issue 46; ISSN 1089-5639
Country of Publication:
United States
Language:
English