The formation of methanol adsorbate as a structure sensitive process was studied on platinum single crystal surfaces. The measurements were performed on reproducibly prepared, clean and either well ordered ("undisturbed") or cycled ("disturbed") Pt(100) and Pt(ll1) single crystal electrodes. Essenti
Microcalorimetric study of ethylene adsorption on the Pt{111} surface
β Scribed by Y.Y. Yeo; A. Stuck; C.E. Wartnaby; D.A. King
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 709 KB
- Volume
- 259
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
The reaction of C2H 4 on Pt{111} at 300 K has been investigated by single crystal adsorption calorimetry. The initial heats of adsorption and the initial sticking probability are 174 kJ/mol and 0.67 respectively. The adsorption heat versus coverage data shows a remarkable minimum which serves as a basis for a mechanism involving ethylidene (CHCH 3) as an intermediate for the formation of ethylidyne (C2H 3) on the Pt{111} surface. The coverage-dependent sticking probability strongly indicates that adsorption is precursor mediated and is well-fitted by the King and Wells expression. From the structure of the decomposition species known to form on the Pt{111} surface, the average C-Pt bond strength is found to be about 245 kJ/mol, although the actual value is found to be species-dependent.
π SIMILAR VOLUMES
HydrogenadsorptiononPt(lOO),Pt(ll 1 l)(6(l00)~(1ll)),Pt(llO)andPt(lll)electrodesurfaceswasstudiedbyboth voltammetry and in situ infrared reflection absorption spectroscopy. The terminal hydrogens adsorbed on Pt( 100)) Pt ( 11 1 1) and Pt( 110) electrodes were observed at 1990-2080 cm-' as bands appe
The coadsorption of C,H, with Hz and CO on Pd(ll1) has been investigated at 300 and 330 K\_ At 300 2; two forms of adsorbed ethylene coexist on the surface in the presence of ethylene gas: a molecular iorm desorbing 3s C2 & at 330 K and a dissociatively adsorbed form (giving only hydrogen in dcsorpt