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  • Title: Hydrazine decomposition over Irn/Al2O3 model catalysts prepared by size-selected cluster deposition.
    Author: Lee S, Fan C, Wu T, Anderson SL.
    Journal: J Phys Chem B; 2005 Jan 13; 109(1):381-8. PubMed ID: 16851026.
    Abstract:
    Hydrazine decomposition chemistry was probed over a temperature range from 100 to 800 K for a series of model catalysts prepared by mass-selected Ir(n)(+) deposition on planar Al(2)O(3)/NiAl(110). Two sets of experiments are reported. Temperature-programmed desorption (TPD) was used to study hydrazine desorption and decomposition on Al(2)O(3)/NiAl(110) and on a model catalyst prepared by deposition of Ir(+) on Al(2)O(3)/NiAl(110) at a density large enough (5 x 10(14) cm(-2)) that formation of a distribution of small Ir(n) clusters on the surface is expected. This model catalyst was found to have hydrazine decomposition properties qualitatively similar to those observed on single-crystal Ir and polycrystalline Rh. This catalyst was also studied by X-ray photoelectron spectroscopy (XPS), to probe TPD-induced changes in the samples. A substantial decrease in the Ir XPS intensity suggests that considerable sintering takes place when the samples are heated to 800 K. In addition, a significant fraction of the nitrogen contained in the hydrazine is converted to an aluminum nitride (or mixed Al(x)O(y)N(z)) compound. Continuous flow experiments were used to probe relative reactivity at 300 and 400 K of samples prepared by depositing differently sized Ir(n)(+) clusters. At 300 K, samples prepared with preformed Ir(n)(+) (n = 5, 7, 10) are about twice as active, per Ir atom, as samples prepared with Ir(+) deposition, and there is a weaker trend to higher activity with increasing cluster size. At 400 K the trends are similar, but weaker, suggesting that thermal modification of the samples is already significant.
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