4.6 Article

Microcalorimetry of oxygen adsorption on fcc Co{110}

期刊

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 14, 期 20, 页码 7528-7532

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2cp40549k

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资金

  1. Cambridge Commonwealth Trust
  2. Shell Global Solutions International B.V.
  3. EPSRC
  4. EPSRC [EP/E039782/1] Funding Source: UKRI
  5. Engineering and Physical Sciences Research Council [EP/E039782/1] Funding Source: researchfish

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The coverage dependent heats of adsorption and sticking probabilities for oxygen on fcc Co{110} have been measured at 300 K using single crystal adsorption calorimetry (SCAC). Initial adsorption is consistent with dissociative chemisorption at low coverage followed by oxide formation above 0.6 ML coverage. The initial heat of adsorption of 633 kJ mol(-1) is similar to heat values calorimetrically measured on other ferromagnetic metal surfaces, such as nickel and iron. As the coverage increases, the heat of adsorption and sticking probability drop very rapidly up to the onset of oxidation. As already observed for other oxygen-metal surface systems, strong lateral adatom repulsions are responsible for the transition from the chemisorption regime to oxide film formation at higher coverage. The heat of oxide formation at the onset is 475 kJ mol(-1), which is consistent with the formation of CoO crystallites. The oxide film formation is discussed in terms of nucleation and island growth, and the Mott-Cabrera mechanisms, the latter being evidenced by the relatively constant heat of adsorption and sticking probability in contrast to the nickel and iron oxidation cases.

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