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Thermal Disproportionation of Oxo-Functionalized Graphene
Authors:Fabian Grote  Christoph Gruber  Dr. Felix Börrnert  Prof. Dr. Ute Kaiser  Prof. Dr. Siegfried Eigler
Affiliation:1. Department of Chemistry and Pharmacy and Central Institute of Materials and Processes (ZMP), Friedrich-Alexander-Universität Erlangen-Nürnberg, FAU, Dr.-Mack Strasse 81, 90762 Fürth, Germany;2. Materialwissenschaftliche Elektronenmikroskopie, Universität Ulm, Albert-Einstein-Allee 11, 89081 Ulm, Germany

IFW Dresden, PF 270116, 01171 Dresden, Germany;3. Materialwissenschaftliche Elektronenmikroskopie, Universität Ulm, Albert-Einstein-Allee 11, 89081 Ulm, Germany;4. Institute of Chemistry and Biochemistry, Freie Universität Berlin, Takustrasse 3, 14195 Berlin, Germany

Abstract:Graphene production by wet chemistry is an ongoing scientific challenge. Controlled oxidation of graphite introduces oxo functional groups; this material can be processed and converted back to graphene by reductive defunctionalization. Although thermal processing yields conductive carbon, a ruptured and undefined carbon lattice is produced as a consequence of CO2 formation. This thermal process is not understood, but it is believed that graphene is not accessible. Here, we thermally process oxo-functionalized graphene (oxo-G) with a low (4–6 %) and high degree of functionalization (50–60 %) and find on the basis of Raman spectroscopy and transmission electron microscopy performed at atomic resolution (HRTEM) that thermal processing leads predominantly to an intact carbon framework with a density of lattice defects as low as 0.8 %. We attribute this finding to reorganization effects of oxo groups. This finding holds out the prospect of thermal graphene formation from oxo-G derivatives.
Keywords:graphene  oxo-functionalized graphene  Raman spectroscopy  reduction  transmission electron microscopy
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