Number of the records: 1  

Angle Resolved X-ray Photoelectron Spectroscopy Study of Au Deposited on Pt and Re Surfaces

  1. 1.
    SYSNO ASEP0101118
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JOstatní články
    TitleAngle Resolved X-ray Photoelectron Spectroscopy Study of Au Deposited on Pt and Re Surfaces
    TitleStudium Au deponovaného na Pt a Re površích metodou úhlově rozlišené fotoelektronové spektroskopie s excitací X-zářením
    Author(s) Bastl, Zdeněk (UFCH-W) RID, ORCID
    Pick, Štěpán (UFCH-W)
    Source TitleSurface Science. - : Elsevier - ISSN 0039-6028
    566-568, - (2004), s. 832-836
    Number of pages5 s.
    Languageeng - English
    CountryNL - Netherlands
    Keywordsphotoelectron spectroscopy ; metal-metal interfaces ; gold and platinum
    Subject RIVCF - Physical ; Theoretical Chemistry
    R&D ProjectsKSK4040110 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    AnnotationThe growth of Au on Pt and Re sputtered and annealed surfaces was investigated by angle resolved XPS method. The shifts of Au 4f core electron binding energy were negative for Au deposited on Pt and higher in magnitude than positive shifts observed for Au on Re. The shifts did not depend on the structure of the Pt substrate surface but were affected by structure of the Re surface. More than 5 equivalent monolayers of Au on Pt were required to obtain bulk-like spectra while 2 monolayers were sufficient for Au/Re. The results suggested formation of several monolayers thick interface Au-Pt alloy in contrast to abrupt Au/Re interface. The measured trends in Au 4f core level shifts were reproduced by those calculated using local density functional method within the initial state approximation.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2005
Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.