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Interaction of nitric oxide with reducing gases on the (100) plane of platinum

Thesis/Dissertation ·
OSTI ID:5593327
The NO + CO and NO + H/sub 2/ reactions on Pt(100) were studied using temperature programmed desorption (TPD), isothermal desorption mass spectrometry, low energy electron diffraction (LEED), and x-ray photoelectron spectroscopy (XPS). Mathematical models were developed to describe the thermal desorption results. These models were then analyzed in an attempt to explain the rate oscillations which occur in the NO + CO reaction on polycrystalline platinum. TPD of NO and CO coadsorbed at 120 K yields almost complete reaction, with both N/sub 2/ and CO/sub 2/ products desorbing at approx. 410 K with full widths at half maximum as narrow as 3 K. Isothermal desorption mass spectrometry yields N/sub 2/ and CO/sub 2/ rates that exhibit a maximum with time. Both experiments indicate that the reaction mechanism is autocatalytic. TPD of NO coadsorbed with H/sub 2/ yields sharp N/sub 2/ and H/sub 2/O product peaks that closely resemble the N/sub 2/ and CO/sub 2/ peaks observed in the NO + CO reaction. LEED experiments during TPD and isothermal desorption of coadsorbed NO and CO indicated that the (1 x 1) ..-->.. hex substrate phase transformation sometimes accompanies desorption of N/sub 2/ and CO/sub 2/. XPS showed that molecular NO and molecular CO are the only species on the surface prior to the onset of reaction in thermal desorption experiments.
Research Organization:
Minnesota Univ., Minneapolis (USA)
OSTI ID:
5593327
Country of Publication:
United States
Language:
English

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