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Mechanisms for ethylene hydrogenation and H-D exchange over Pt(111)

Journal Article · · Journal of Physical Chemistry; (USA)
DOI:https://doi.org/10.1021/j100375a061· OSTI ID:6330977
 [1]
  1. Univ. of California, Riverside (USA)

TPD data for C{sub 2}D{sub 4} and C{sub 2}D{sub 3}H chemisorbed over Pt(111) single-crystal surfaces have provided further insight into the mechanisms of ethylene hydrogenation and H-D exchange under ultrahigh vacuum. Desorption of C{sub 2}D{sub 6} from adsorbed C{sub 2}D{sub 4} clearly proves that ethylene undergoes self-hydrogenation by starting with a C-D bond breaking step which provides deuterium atoms to other ethylene molecules. This is the rate-limiting step for both hydrogenation and ethylidyne formation. Coadsorbed hydrogen (or deuterium) increases the ethane yield and lowers the apparent activation energy for that reaction. When H{sub 2} and C{sub 2}D{sub 4} are coadsorbed, hydrogenation and H-D exchange occur simultaneously through the formation of a common intermediate which we believe is an ethyl group.

OSTI ID:
6330977
Journal Information:
Journal of Physical Chemistry; (USA), Journal Name: Journal of Physical Chemistry; (USA) Vol. 94:12; ISSN 0022-3654; ISSN JPCHA
Country of Publication:
United States
Language:
English