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Title: Infrared spectroscopic investigation of the ethylene chemisorption reaction on supported metallic catalyst surfaces: ethylidyne formation on Pt, Rh, Pd, and Ru supported on alumina

Journal Article · · J. Phys. Chem.; (United States)
DOI:https://doi.org/10.1021/j100286a003· OSTI ID:6874795

The reaction of ethylene with Pt, Rh, Pd, and Ru supported on alumina has been studied at 300 K by transmission infrared spectroscopy. Small metal particles of all four elements form the ethylidyne species, identical with CCH/sub 3/, and the vibrational frequencies of these species are in close agreement with those reported for ethylidyne adsorbed on the close-packed faces of single crystals of these same metals. The authors PT and Rh surface produce ethylidyne IR bands of higher intensity than Pd and Ru. This is consistent with the presence of smaller Pt and Rh average particle sizes, where quantitative CO adsorption measurements indicate an approximately 2- to 3-fold greater chemisorption capacity of Pt and Rh surfaces than Pd and Ru surfaces. In addition, Pt and Rh surfaces exhibit relatively strong ethylidyne asymmetric modes (nu/sub as/(CH/sub 3/) and sigma/sub as/(CH/sub 3/)), indicating that the surface-dipole selection rule is not strictly in operation on these surfaces. This weakening of the selection rule for Pt and Rh surfaces is consistent with the small average particle sizes for Pt and Rh (19 and 28 A, respectively) compared to larger average particle sizes for Pd and Rh (84 and 66 A, respectively).

Research Organization:
Univ. of Pittsburgh, PA
OSTI ID:
6874795
Journal Information:
J. Phys. Chem.; (United States), Vol. 91:2
Country of Publication:
United States
Language:
English