No Chemisorption on Ni(111): Coverage Effects, Site Preferences and Adsorption Geometry.

Abstract

Several possible rationales for the different NO adsorption states observed on a Ni(111) surface are discussed, based on the tight binding calculations of the extended Huckel type. In the two-fold bridge site, as the coverage of NO increases, for perpendicularly adsorbed NO the N-O bonding increases and N-Ni bonding decreases. For slightly bent NO at low coverage and perpendicular NO at high coverage the same trends are obtained. These trends are consistent with the observed N-O, N-Ni stretching frequency change. At coverage 1/3, and in the perpendicular geometry, both N-O bonding and N-Ni bonding increase when NO changes adsorption sites form three-fold to two-fold or from two-fold to on-top. In the on-top site we calculate that both N-O bonding and N-Ni bonding increase when NO changes geometry from bent to perpendicular. In the two-fold bridge site the effect of bending is to produce similar but smaller trends. (Author)

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Document Details

Document Type
Technical Report
Publication Date
Sep 03, 1985
Accession Number
ADA159110

Entities

People

  • P. A. Thiel
  • Robert R. Hoffman
  • S. S. Sung

Organizations

  • Cornell University Department of Chemistry and Chemical Biology

Tags

Communities of Interest

  • Energy and Power Technologies

DTIC Thesaurus Topics

  • Adsorption
  • Band Structures
  • Chemisorption
  • Chemistry
  • Crystal Structure
  • D Band
  • Electron Density
  • Electrons
  • Energy Bands
  • Fermi Levels
  • Frequency
  • Frequency Shift
  • Geometry
  • Spectra
  • Transition Metals
  • Transitions
  • Vibrational Spectra

Readers

  • Quantum Chemistry
  • Thin Film Deposition Science.