科研之友
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摘要
Kinetic and isotopic methods were used to establish the identity and kinetic relevance of elementary steps and the effects of cluster size for NO oxidation on supported Pd catalysts. O(2) activation on vacancies within nearly saturated oxygen adlayers is the sole kinetically relevant step. Water, present in combustion effluents, inhibits NO oxidation via reversible adsorption on vacancies to form unreactive OH species. The coverage and chemical potential of oxygen are determined by the NO(2)/NO ratios prevalent during catalysis; they are rigorously described by O(2) virtual pressures accessible to measurement. At a given oxygen chemical potential, O(2) activation during (16)O(2)-(18)O(2) exchange and NO oxidation occurs at similar rates, indicating that NO-assisted O(2) activation is not required for NO oxidation turnovers. These findings confirm the rigor and relevance of O(2) virtual pressure as a measurable surrogate for the oxygen chemical potential during catalysis, as well as the role of mobile oxygen species, which allow O(2) dissociation to occur on isolated vacancies. Oxygen chemical potentials prevalent during NO oxidation cause active clusters to exist as PdO at all relevant conditions, consistent with steady-state turnover rates that are insensitive to reductive or oxidative treatments. NO oxidation turnover rates decrease as PdO clusters become smaller because of stronger oxygen binding and lower vacancy concentrations in small clusters. The catalytic consequences of size are similar on PdO and Pt clusters, despite their different oxidation state, consistent with a common requirement for surface vacancies in O(2) activation steps on both catalysts. Such requirements lead to strong NO(2) inhibition effects and to a marked increase in NO oxidation rates when NO(2) adsorbents, present as physical mixtures, decrease NO(2) concentrations near active sites.
- 出版日期2010-5-25
