Reactivity and selectivity descriptors of dioxygen activation routes on metal oxides

• Published in: Journal of catalysis Vol. 377; no. C; pp. 692 - 710
• Main Authors: Kwon, Stephanie, Deshlahra, Prashant, Iglesia, Enrique
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01-09-2019; Elsevier
• Subjects: Density functional theory; Dioxygen activation; Metal oxides; Oxidation catalysis; Redox cycle; Metal oxides; Density functional theory; Redox cycle; Oxidation catalysis; Dioxygen activation
• ISSN: 0021-9517; 1090-2694
• DOI: 10.1016/j.jcat.2019.07.048

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•Two-electron reduced centers formed on metal oxides in redox cycles activate O2 via inner or outer sphere routes.•Inner sphere routes form bound peroxo species at O-vacancies.•Outer sphere routes form H2O2(g) at vicinal OH pairs, formed via H2O dissociation on O-vacancies.•The O-atoms in more reducible oxides exhibit a greater preference for the inner sphere routes.•The large charge-balancing cations influence the O2 activation selectivity of the vicinal O-atoms.
The activation of dioxygen at typically isolated two-electron reduced centers can lead to the formation of electrophilic superoxo or peroxo species, providing an essential route to form reactive O2-derived species in biological, organometallic, and heterogeneous catalysts. Alternatively, O2 activation can proceed via outer sphere routes, circumventing the formation of bound peroxo (OO*) species during oxidation catalysis by forming H2O2(g), which can react with another reduced center to form H2O. The electronic and binding properties of metal oxides that determine the relative rates of these activation routes are assessed here by systematic theoretical treatments using density functional theory (DFT). These methods are combined with conceptual frameworks based on thermochemical cycles and crossing potential models to assess the most appropriate descriptors for the activation barriers for each route using Keggin polyoxometalates as illustrative examples. In doing so, we show that inner sphere routes, which form OO* species via O2 activation on the O-vacancies (*) formed in the reduction part of redox cycles, are mediated by early transition states that only weakly sense the oxide binding properties. Outer sphere routes form H2O2(g) via O2 activation on OH pairs (H/OH*) formed by dissociation of H2O on O-vacancies; their rates and activation barriers reflect the rates of the first H-atom transfer from H/OH* to O2. The activation barriers for this H-transfer step depend on the binding energy of more weakly-bound H-atom in H/OH* pairs (HAE2) and on the OOH-surface interaction energy at its product state (Eint0). The Eint0 values are similar among oxides unless a large charge-balancing cation is present and interacts with OOH; consequently, HAE2 acts as an appropriate descriptor of the outer sphere dynamics. HAE2 also determines the thermodynamics of H2O dissociation on O-vacancies, which influence the inner and outer sphere rates by setting the relative coverage of * and H/OH*. These results, in turn, show that HAE2 is a complete descriptor of the reactivity and selectivity of oxides for O2 activation; the O-atoms in more reducible oxides (more negative HAE2) exhibit a greater preference for the inner sphere routes and for the formation of electrophilic OO* intermediates that mediate epoxidation and O-insertion reactions during catalytic redox cycles. Large charge-balancing cations locally modify Eint0 values that determine the outer sphere rates and thus can be used to alter the preference of O-atoms to either inner or outer sphere routes.