Oxygen adsorption on the LaB6(100), (110) and (111) surfaces

R. Nishitani*, C. Oshima, M. Aono, T. Tanaka, S. Kawai, H. Iwasaki, S. Nakamura

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    26 Citations (Scopus)

    Abstract

    Oxygen adsorption on the LaB6(100), (110) and (111) clean surfaces has been studied by means of UPS, XPS and LEED. The results on oxygen adsorption will be discussed on the basis of the structurs and the electronic states on the LaB6(100), (110) and (111) clean surfaces. The surface states on LaB6(110) disappear at the oxygen exposure of 0.4 L where a c(2 × 2) LEED pattern disappears and a (1 × 1) LEED pattern appears. The work function on LaB6(110) is increased to ∼3.8 eV by an oxygen exposure of ∼2 L. The surface states on LaB6(111) disappear at an oxygen exposure of ∼2 L where the work function has a maximum value of ∼4.4 eV. Oxygen is adsorbed on the surface boron atoms of LaB6(111) until an exposure of ∼2 L. Above this exposure, oxygen is adsorbed on another site to lower the work function from ∼4.4 to ∼3.8 eV until an oxygen exposure of ∼100L. The initial sticking coefficient on LaB6(110) has the highest value of ∼1 among the (100), (110) and (111) surfaces. The (100) surface is most stable to oxygen among these surfaces. It is suggested that the dangling bonds of boron atoms play an important role in oxygen adsorption on the LaB6 surfaces.

    Original languageEnglish
    Pages (from-to)48-60
    Number of pages13
    JournalSurface Science
    Volume115
    Issue number1
    DOIs
    Publication statusPublished - 1982 Feb 2

    ASJC Scopus subject areas

    • Physical and Theoretical Chemistry
    • Condensed Matter Physics
    • Surfaces and Interfaces

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