A new method for analysis of reactive adsorbed intermediates: Bismuth postdosing in thermal desorption mass spectroscopy
- 15 May 1988
- journal article
- conference paper
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 88 (10) , 6585-6593
- https://doi.org/10.1063/1.454445
Abstract
A new method which should have relatively general applicability for the identification and quantitative analysis of reactive adsorbed molecular intermediates in surface reactions will be described, and the first examples of its application will be presented. When a reactive intermediate is generated on a surface, it often has a tendency to dissociate before desorbing. Since dissociation generally requires additional free sites on the surface, dissociation can be suppressed and desorption correspondingly enhanced if the free sites on the surface can be properly poisoned. We have found that bismuth adatoms are very good inert site blockers, which can be postdosed to the surface of a transition metal containing a reactive adsorbed hydrocarbon without destroying the hydrocarbon. Whereas in the absence of bismuth, the hydrocarbon would completely dehydrogenate during thermal desorption spectroscopy (TDS) and liberate only H2 into the gas phase, after bismuth postdosing the reactive hydrocarbon desorbs intact for mass spectral identification and quantitative analysis. This method has been used to prove that adsorbed benzene is the initial product of the dehydrogenation of cyclohexane on Pt(111) at ∼235 K. In the absence of bismuth, this benzene all dissociates during TDS to liberate only H2, leaving graphitic carbon residue on the surface. When one‐third monolayer of Bi is postdosed at 110 K, the dehydrogenation pathway is sterically poisoned and the adsorbed benzene quantitatively desorbs during TDS, where it is unambiguously identified by mass spectroscopy. By briefly heating the reactive adsorbed intermediate to increasing temperatures prior to Bi deposition, the thermal stability limits of the intermediate and the kinetic parameters for its dissociation can be established. This is demonstrated for the dehydrogenation reaction of adsorbed cyclopentene on Pt(111). Bismuth postdosing in thermal desorption mass spectroscopy (BPTDS) should be a very useful but inexpensive addition to surface analytical capabilities.Keywords
This publication has 12 references indexed in Scilit:
- Stabilization of C2Dx fragments by CO on Ni(100)Surface Science, 1987
- A tabulation of the infrared spectra of species adsorbed on well-defined surfacesJournal of Electron Spectroscopy and Related Phenomena, 1986
- Vibrations measured at surfaces by high resolution electron energy loss spectroscopy : updated review (1982–1985)Journal of Electron Spectroscopy and Related Phenomena, 1986
- Ethylene and acetylene adsorption on a Pt(111) face: Comparative Δφ and coverage measurementsSurface Science, 1986
- Hydrogen isotope exchange in alkylidynes on Pt(111)Surface Science, 1986
- Bonding and reactivity of cyclopentene on Pt(111)Surface Science, 1984
- The interaction of oxygen with Bi(0001): Kinetic, electronic, and structural featuresSurface Science, 1983
- Mass spectrometry at low electron beam energies: A sensitive probe of vibrational excitationChemical Physics Letters, 1982
- Dehydrogenation processes on nickel and platinum surfaces. Conversion of cyclohexane, cyclohexene, and cyclohexadiene to benzeneJournal of the American Chemical Society, 1982
- CH Vibration Softening and the Dehydrogenation of Hydrocarbon Molecules on Ni(111) and Pt(111)Physical Review Letters, 1978