Evidence for an Oxygen Intermediate in the Catalytic Reduction of NO by CO on Rhodium Surfaces.

Abstract

Evidence for an oxygen intermediate in the reaction of NO and CO to form N2 and CO2 over rhodium surfaces is presented. High resolution electron energy loss spectroscopy (ELS) measurements indicate that both NO and CO molecules associatively adsorb on the Rh(331) single crystal surface at 300 K. Chemisorbed NO readily dissociates on this surface upon heating at 450 K. At 700 K high resolution ELS and Auger electron spectroscopy (AES) both indicate that only oxygen is present on the catalyst surface. N2 desorption below this temperature is easily detected by mass spectroscopy. The addition of CO to this surface oxygen at 700 K results in the formation of gaseous CO2 and the removal of the surface oxygen species. Similar results were obtained when O2 was substituted for NO as a control indicating that oxygen is indeed a surface intermediate under our experimental conditions. (Author)

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Document Details

Document Type
Technical Report
Publication Date
Jul 29, 1980
Accession Number
ADA088045

Entities

People

  • G. A. Somorjai
  • L. H. Dubois
  • Paul K. Hansma

Organizations

  • University of California, Santa Barbara

Tags

Communities of Interest

  • Energy and Power Technologies

DTIC Thesaurus Topics

  • Auger Electron Spectroscopy
  • Auger Electrons
  • Carbon Monoxide
  • Catalysis
  • Chemical Reactions
  • Chemistry
  • Dielectric Gases
  • Electron Energy
  • Electron Spectroscopy
  • Mass Spectrometers
  • Materials
  • Materials Science
  • Nitrogen Oxides
  • Spectra
  • Spectrometry
  • Spectroscopy
  • Vibrational Spectra

Readers

  • Electrochemical Engineering/ Fuel Cell Technologies

Technology Areas

  • Microelectronics