| Abstrakt: |
The recent development of new synthesis techniques has allowed the production of monodisperse metal clusters composed of a few atoms. Follow-up experimental spectroscopic characterization has indicated the stability of these atomic metal clusters (AMCs). Despite the common assumption that the occurrence of an irreversible oxidation becomes more likely as the cluster size decreases, its quenching and reversible nature has been experimentally identified in the particular case of Cu 5 clusters, making them paradigmatic. This work aims to address the influence of aggregation and the effects of a chemically inert carbon-based support on the oxidation of AMCs, considering the case of Cu 5 as a model system. For this purpose, we present an extended first-principles study of the oxidation of Cu 5 -Cu 5 and circumpyrene-supported Cu 5 , comparing it with that of unsupported Cu 5 , and combine dispersion-corrected density-functionals, first principles thermochemistry, and ab initio molecular dynamics (AIMD) simulations within an adiabatic approach. Our results indicate that a molecular chemisorption/desorption model is sensible upon consideration of aggregation and support effects in such a way that the predicted ( p - T )-phase diagrams do not differ significantly from those obtained for unsupported Cu 5 . We also provide insights into the decoupling of the Cu 5 -Cu 5 dimer into Cu 5 sub-units through activated fluxional rotational motion, upon heating, as well as the adsorption of multiple O 2 molecules at high oxygen gas pressures. Furthermore, numerical evidence shows the likelihood of a support-mediated mechanism leading to the dissociation of chemisorbed peroxo O 2 2- species, delivering states with very similar energies to those characterized by molecular chemisorption. A Boltzmann-weighted average of the free energies of formation is computed as well, coming up with a diagram of the dominant copper oxidation states as a function of temperature and oxygen gas pressure. |
