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Surface refinement and electronic properties of graphene layers grown on copper substrate: An XPS, UPS and EELS study

  1. 1.
    SYSNO ASEP0362878
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleSurface refinement and electronic properties of graphene layers grown on copper substrate: An XPS, UPS and EELS study
    Author(s) Siokou, A. (GR)
    Ravani, F. (GR)
    Karakalos, S. (GR)
    Frank, Otakar (UFCH-W) RID, ORCID
    Kalbáč, Martin (UFCH-W) RID, ORCID
    Galiotis, C. (GR)
    Source TitleApplied Surface Science. - : Elsevier - ISSN 0169-4332
    Roč. 257, č. 23 (2011), s. 9785-9790
    Number of pages6 s.
    Languageeng - English
    CountryNL - Netherlands
    Keywordsgraphene ; XPS ; EELS
    Subject RIVCG - Electrochemistry
    R&D ProjectsLC510 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    IAA400400911 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    CEZAV0Z40400503 - UFCH-W (2005-2011)
    UT WOS000293883400016
    DOI10.1016/j.apsusc.2011.06.017
    AnnotationThe present work focuses on the assessment of two surface treatment procedures employed under ultra high vacuum conditions in order to obtain atomically clean graphene layers without disrupting the morphology and the two dimensional character of the films. Graphene layers grown by chemical vapor deposition on polycrystalline Cu were stepwise annealed up to 750 °C or treated by mild Ar+ sputtering. The effectiveness of both methods and the changes that they induce on the surface morphology and electronic structure of the films were systematically studied by X-ray photoelectron spectroscopy, and electron energy loss spectroscopy. Ultraviolet photoelectron spectroscopy was employed for the study of the electronic properties of the as received sample and in combination with the work function measurements, indicated the hybridization of the C–π network with Cu d-orbitals. Mild Ar+ sputtering sessions were found to disrupt the sp2 network and cause amorphisation of the graphitic carbon.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2012
Number of the records: 1  

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