Giant edge state splitting at atomically precise graphene zigzag edges

Zigzag edges of graphene nanostructures host localized electronic states that are predicted to be spin-polarized. However, these edge states are highly susceptible to edge roughness and interaction with a supporting substrate, complicating the study of their intrinsic electronic and magnetic structu...

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Published inNature communications Vol. 7; no. 1; p. 11507
Main Authors Wang, Shiyong, Talirz, Leopold, Pignedoli, Carlo A., Feng, Xinliang, Müllen, Klaus, Fasel, Roman, Ruffieux, Pascal
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 16.05.2016
Nature Publishing Group
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Summary:Zigzag edges of graphene nanostructures host localized electronic states that are predicted to be spin-polarized. However, these edge states are highly susceptible to edge roughness and interaction with a supporting substrate, complicating the study of their intrinsic electronic and magnetic structure. Here, we focus on atomically precise graphene nanoribbons whose two short zigzag edges host exactly one localized electron each. Using the tip of a scanning tunnelling microscope, the graphene nanoribbons are transferred from the metallic growth substrate onto insulating islands of NaCl in order to decouple their electronic structure from the metal. The absence of charge transfer and hybridization with the substrate is confirmed by scanning tunnelling spectroscopy, which reveals a pair of occupied/unoccupied edge states. Their large energy splitting of 1.9 eV is in accordance with ab initio many-body perturbation theory calculations and reflects the dominant role of electron–electron interactions in these localized states. The zigzag edges of graphene host edge-localized electronic states with aligned electron spins, but these states strongly interact with metallic substrates. Here, the authors measure the electronic structure of graphene nanoribbons after transferring them to an insulating support.
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These authors contributed equally to this work
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms11507