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Adsorption and reactions of benzenethiol on the Ni(111) surface

Journal Article · · Journal of Physical Chemistry; (United States)
DOI:https://doi.org/10.1021/j100100a034· OSTI ID:6879029
;  [1]; ;  [2]
  1. Univ. of Michigan, Ann Arbor, MI (United States)
  2. Oak Ridge National Lab., TN (United States)
The adsorption and reactions of benzenethiol have been analyzed on the Ni(111) surface using TPD, XPS, LEED and HREELS. At 110 K, benzenethiol absorbs on the surface through the surface atom. The vibrational data indicate that the S-H bond in benzenethiol breaks upon adsorption at 110 K for all exposures. The primary surface intermediate observed for high coverages of benzenethiol at 190 K is phenyl thiolate. HREELS results indicate that the aromatic ring in phenyl thiolate is neither parallel nor perpendicular to the surface, but tilted. For low coverages of benzenethiol, decomposition of the molecule to gaseous hydrogen, atomic sulfur, and carbon is the favored reaction pathway, while benzene formation is the dominant reaction for higher coverages. Two pathways are observed for the desorption of the benzene product. At intermediate coverages a desorption-limited process occurs near 400 K, while at high coverages benzene desorption is limited by hydrogenolysis of phenyl thiolate at 263 K. Above 300 K, a stable aromatic hydrocarbon intermediate, most likely a phenyl fragment, is observed on the sulfur-covered Ni(111) surface. 32 refs., 6 figs., 1 tab.
OSTI ID:
6879029
Journal Information:
Journal of Physical Chemistry; (United States), Journal Name: Journal of Physical Chemistry; (United States) Vol. 98:49; ISSN JPCHAX; ISSN 0022-3654
Country of Publication:
United States
Language:
English