Graphene nanoribbons (GNRs) with an unprecedented “necklace-like” structure were synthesized through a bottom-up chemical approach, based on the oxidative cyclodehydrogenation of tailor-made polyphenylene precursors. A polycyclic aromatic hydrocarbon consisting of 84 sp2 carbons (C84) was also synthesized and characterized as a model compound. Characterizations by a combination of MALDI-TOF MS and FTIR, Raman, and UV/Vis absorption spectroscopy validated the formation of the necklace-like GNRs. The absorption spectrum and DFT calculations revealed a bandgap of approximately 1.4 eV for this novel GNR system, which has not been attained with other GNR structures, enabling further fine-tuning of GNR bandgaps by structural modulation.

Bottom-Up Synthesis of Necklace-Like Graphene Nanoribbons

MAGHSOUMI, ALI;CASTIGLIONI, CHIARA;TOMMASINI, MATTEO MARIA SAVERIO;
2015-01-01

Abstract

Graphene nanoribbons (GNRs) with an unprecedented “necklace-like” structure were synthesized through a bottom-up chemical approach, based on the oxidative cyclodehydrogenation of tailor-made polyphenylene precursors. A polycyclic aromatic hydrocarbon consisting of 84 sp2 carbons (C84) was also synthesized and characterized as a model compound. Characterizations by a combination of MALDI-TOF MS and FTIR, Raman, and UV/Vis absorption spectroscopy validated the formation of the necklace-like GNRs. The absorption spectrum and DFT calculations revealed a bandgap of approximately 1.4 eV for this novel GNR system, which has not been attained with other GNR structures, enabling further fine-tuning of GNR bandgaps by structural modulation.
2015
Dehydrogenation; Graphene; Nanostructures; Polycycles; Vibrational spectroscopy; Chemistry (all)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11311/969598
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