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Oxidation kinetics for Ni(111) and the structure of the oxide layers

Journal Article · · Physical Review. B, Condensed Matter and Materials Physics
 [1]; ; ;  [2]
  1. National Institute of Advanced Industrial Science and Technology, AIST Kansai, Midorigaoka, Ikeda, Osaka 563-8577 (Japan)
  2. Department of Physics, Ritsumeikan University, Kusatsu, Shiga-ken 525-8577 (Japan)
The oxidation kinetics for Ni(111) surface and the structure of the oxide layers grown at room temperature were analyzed by high-resolution medium energy ion scattering using isotopically labeled {sup 18}O{sub 2}. Initially, the surface showed a reflection high energy electron diffraction (RHEED) pattern of the Ni(111)-(2x2)-O chemisorption structure at an oxygen exposure of a few langmuir (1 L:10{sup -6} Torr s) and started to form NiO(111) layers above 10 L. The oxide thickness was saturated with six atomic layers at oxygen exposure of 160 L. The saturated NiO(111) surface shows a (1x1) RHEED pattern not p(2x2) and consists of two domains: NiO(111)-[112]//Ni(111)-[112] (primary) and NiO(111)-[110]//Ni(111)-[112](a small fraction). The elemental depth profile corresponds to the octopolar reconstruction terminated with Ni (0.25 ML) [1 ML=1.33x10{sup 15} atoms/cm{sup 2}: areal density of NiO(111)]. The oxide surface grown epitaxially probably takes a precursor state of the octopolar structure with significant distortion because of a large lattice mismatch of 19% between NiO(111) and Ni(111). Tow step oxidation using {sup 18}O{sub 2} and {sup 16}O{sub 2} clearly indicates that oxidation takes place at the top surface obeying the Cabrera-Mott mechanism. The potential barrier for the jump from Ni into the NiO layer is derived to be 2.36 eV.
OSTI ID:
20976653
Journal Information:
Physical Review. B, Condensed Matter and Materials Physics, Journal Name: Physical Review. B, Condensed Matter and Materials Physics Journal Issue: 3 Vol. 75; ISSN 1098-0121
Country of Publication:
United States
Language:
English