Abstract

Chiral graphene nanoribbons are extremely interesting structures due to their narrow band gaps and potential development of spin-polarized edge states. Here, we study their band structure on low work function silver surfaces. The use of a curved Ag single crystal provides, within the same sample, regions of disparate step structure and step density. Whereas the former leads to distinct azimuthal growth orientations of the graphene nanoribbons atop, the latter modulates the substrate’s work function and thereby the interface energy level alignment. In turn, we disclose the associated charge transfer from the substrate to the ribbon and assess its effect on the nanoribbon’s properties and the edge state magnetization.

Highlights

  • IntroductionCarbon-based nanostructures can display exceptionally varied properties depending on their precise bonding structure

  • Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations

  • Carbon-based nanostructures can display exceptionally varied properties depending on their precise bonding structure. This includes graphene nanoribbons (GNRs) [1,2,3], in which a graphene lattice is confined to narrow, one-dimensional stripes

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Summary

Introduction

Carbon-based nanostructures can display exceptionally varied properties depending on their precise bonding structure. This includes graphene nanoribbons (GNRs) [1,2,3], in which a graphene lattice is confined to narrow, one-dimensional stripes. Zigzag and even chiral GNRs are quasi-metallic and develop spin-polarized edge states [2,3,4,5], unless they are exceedingly narrow In this case, the edge states from either side hybridize with one another, which quenches the spin polarization and confers the ribbons a conventional semiconducting band structure [6,7]

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