Large-scale solution synthesis of narrow graphene nanoribbons
Timothy H. Vo,
Mikhail Shekhirev,
Donna A. Kunkel,
Martha D. Morton,
Eric Berglund,
Lingmei Kong,
Peter M. Wilson,
Peter A. Dowben,
Axel Enders and
Alexander Sinitskii ()
Additional contact information
Timothy H. Vo: University of Nebraska–Lincoln
Mikhail Shekhirev: University of Nebraska–Lincoln
Donna A. Kunkel: University of Nebraska–Lincoln
Martha D. Morton: University of Nebraska–Lincoln
Eric Berglund: University of Nebraska–Lincoln
Lingmei Kong: University of Nebraska–Lincoln
Peter M. Wilson: University of Nebraska–Lincoln
Peter A. Dowben: University of Nebraska–Lincoln
Axel Enders: University of Nebraska–Lincoln
Alexander Sinitskii: University of Nebraska–Lincoln
Nature Communications, 2014, vol. 5, issue 1, 1-8
Abstract:
Abstract According to theoretical studies, narrow graphene nanoribbons with atomically precise armchair edges and widths of 10 nm and have limited control over their edge structure. Here we demonstrate a novel bottom–up approach that yields gram quantities of high-aspect-ratio graphene nanoribbons, which are only ~1 nm wide and have atomically smooth armchair edges. These ribbons are shown to have a large electronic bandgap of ~1.3 eV, which is significantly higher than any value reported so far in experimental studies of graphene nanoribbons prepared by top–down approaches. These synthetic ribbons could have lengths of >100 nm and self-assemble in highly ordered few-micrometer-long ‘nanobelts’ that can be visualized by conventional microscopy techniques, and potentially used for the fabrication of electronic devices.
Date: 2014
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms4189
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DOI: 10.1038/ncomms4189
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