Photoemission Studies of Time-Resolved Surface Reactions: Isothermal Desorption of Co from Ni (111).

Abstract

A new dynamic approach to spectroscopic studies of surface reactions is described. A fast-acting UHV gas dosing system is employed to prepare the adsorbed species in an initial chemisorption state under reaction conditions of elevated temperature and/or pressure (to approximately 1 torr). Individual reaction steps are then resolved in time using photoemission spectroscopy to probe the surface electronic structure, yielding information about the kinetics of individual reaction steps, the nature of chemisorbed species, and the surface reaction path. As a result application of this approach, the kinetics of isothermal desorption of CO from Ni(111) is studied for temperatures up to approximately 230 degrees C. The coverage-dependence of the rate constants is revealed directly in the shape of each desorption curve. Preexponential (frequency) factors as well as desorption activation energies show significant variation with coverage. (Author)

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Document Details

Document Type
Technical Report
Publication Date
Feb 27, 1979
Accession Number
ADA074953

Entities

People

  • G. W. Rubloff

Organizations

  • IBM Thomas J. Watson Research Center

Tags

Communities of Interest

  • Energy and Power Technologies

DTIC Thesaurus Topics

  • Adsorption
  • Chemistry
  • Desorption
  • Energy
  • Frequency
  • Heat Of Activation
  • Kinetics
  • Measurement
  • Military Research
  • Mining Engineering
  • New York
  • Photoelectric Emission
  • Physics
  • Reaction Time
  • Saturation
  • Spectroscopy
  • Surface Reactions

Fields of Study

  • Physics

Readers

  • Electrochemical Engineering/ Fuel Cell Technologies
  • Molecular Photonics/Laser Physics
  • Thin Film Deposition Science.

Technology Areas

  • Microelectronics