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Title: Structural studies of molecular and metallic overlayers using angle- resolved photoemission extended fine structure

Thesis/Dissertation ·
DOI:https://doi.org/10.2172/10110509· OSTI ID:10110509
 [1]
  1. Univ. of California, Berkeley, CA (United States)

Angle-resolved photoemission extended fine structure (ARPEFS) was used to study molecular and metallic overlayers on metal surfaces through analysis of p2mg(2x1)CO/Ni(110) and the p(2x2)K/Ni(111) adsorption. For the dense p2mg(2x1)CO/Ni(110) surface layer, photoemission intensities from C 1s level were measured in three directions at photoelectron kinetic energies 60-400 eV. Using multiple-scattering spherical-wave (MSSW) modeling, it was found that CO molecules are adsorbed on short-bridge sites, with adjacent CO along the [110] direction displaced alternatively in opposite directions towards the [001] azimuths to form a zigzag chain geometry. The tilt angle is 16±2° from the surface normal for the direction linking the C atom and the center of the Ni bridge. The carbon C-Ni interatomic distance was determined to be 1.94±0.02Å. The first- to second-layer spacing of Ni is 1.27±0.04Å, up from 1.10Å for the clean Ni(110) surface, but close to the 1.25Å Ni interlayer spacing in the bulk. The C-O bond length and tilt angle were varied within small ranges (1.10--1.20Å and 15--23°) in our MSSW simulations. Best agreement between experiment and simulations was achieved at 1.16Å and 19°. This yields an O-O distance of 2.95Å for the two nearest CO molecules, (van der Waals` radius ~ 1.5 Å for oxygen). Two different partial-wave phase-shifts were used in MSSW, and structural results from both are in very good agreement. For the p(2x2)K/Ni(111) overlayer, ARPEFS {chi}(k) curves from K 1s level measured along [111] and [771] at 130K showed that the K atoms are preferentially adsorbed on the atop sites, in agreement with a LEED study of the same system.

Research Organization:
Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)
Sponsoring Organization:
USDOE
DOE Contract Number:
AC03-76SF00098
OSTI ID:
10110509
Report Number(s):
LBL-33040; ON: DE93004700
Resource Relation:
Other Information: TH: Thesis (Ph.D.); PBD: Oct 1992
Country of Publication:
United States
Language:
English