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In Situ Observations of the Atomistic Mechanisms of Ni Catalyzed Low Temperature Graphene Growth

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http://pubman.mpdl.mpg.de/cone/persons/resource/persons21743

Knop-Gericke,  Axel
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons22071

Schlögl,  Robert
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Citation

Patera, L., Africh, C., Weatherup, R., Blume, R., Bhardwaj, S., Castellarin-Cudia, C., et al. (2013). In Situ Observations of the Atomistic Mechanisms of Ni Catalyzed Low Temperature Graphene Growth. ACS Nano, 7(9), 7901-7912. doi:10.1021/nn402927q.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0014-1CFC-5
Abstract
The key atomistic mechanisms of graphene formation on Ni for technologically relevant hydrocarbon exposures below 600°C are directly revealed via complementary in situ scanning tunneling microscopy and X-ray photoelectron spectroscopy. For clean Ni(111) below 500°C, two different surface carbide (Ni2C) conversion mechanisms are dominant which both yield epitaxial graphene, whereas above 500°C graphene predominantly grows directly on Ni(111) via replacement mechanisms leading to embedded epitaxial and/or rotated graphene domains. Upon cooling, additional carbon structures form exclusively underneath rotated graphene domains. The dominant graphene growth mechanism also critically depends on the near-surface carbon concentration and hence is intimately linked to the full history of the catalyst and all possible sources of contamination. The detailed XPS fingerprinting of these processes allows a direct link to high pressure XPS measurements of a wide range of growth conditions, including polycrystalline Ni catalysts and recipes commonly used in industrial reactors for graphene and carbon nanotube CVD. This enables an unambiguous and consistent interpretation of prior literature and an assessment of how the quality/structure of as-grown carbon nanostructures relates to the growth modes.