Electronic structure study of ordering and interfacial interaction in graphene/Cu composites

Graphene CVD-grown on Cu has been studied using Raman spectroscopy, X-ray absorption spectroscopy (XAS) and X-ray emission spectroscopy (XES). Raman data indicate the presence of weak compressive strain at the interface of graphene/Cu. Compared with highly ordered pyrolytic graphite (HOPG), new elec...

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Published inCarbon (New York) Vol. 50; no. 14; pp. 5316 - 5322
Main Authors Zhang, Liang, Pollak, Elad, Wang, Wei-Cheng, Jiang, Peng, Glans, Per-Anders, Zhang, Yuegang, Cabana, Jordi, Kostecki, Robert, Chang, Chinglin, Salmeron, Miquel, Zhu, Junfa, Guo, Jinghua
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier Ltd 01.11.2012
Elsevier
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Summary:Graphene CVD-grown on Cu has been studied using Raman spectroscopy, X-ray absorption spectroscopy (XAS) and X-ray emission spectroscopy (XES). Raman data indicate the presence of weak compressive strain at the interface of graphene/Cu. Compared with highly ordered pyrolytic graphite (HOPG), new electronic states in the conduction band are observed for graphene/Cu, which are mainly ascribed to the defect states and interfacial interaction between the single graphene layer and Cu surface. Moreover, polarization dependent XAS measurements demonstrate that the graphene/Cu exhibits a high degree of alignment and weak corrugation on the surface. Significant intensity modulation in the resonant XES spectral shape upon different excitation energies near the C K-edge indicates that graphene layer preserves an intrinsic momentum as that of HOPG and the interaction between graphene and Cu shows weak influence on the valence band structure of graphene. However, broad inelastic features and subtle peak shifts are observed in the resonant XES spectra of graphene/Cu in comparison of HOPG, which can be mainly attributed to the electron–phonon scattering and charge transfer from the interfacial interaction of graphene and Cu substrate.
Bibliography:ObjectType-Article-2
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USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22)
SC0001294
ISSN:0008-6223
1873-3891
DOI:10.1016/j.carbon.2012.07.020