Contributing to the need for new
graphene nanoribbon (GNR) structures
that can be synthesized with atomic precision, we have designed a
reactant that renders chiral (3,1)-GNRs after a multistep reaction
including Ullmann coupling and cyclodehydrogenation. The nanoribbon
synthesis has been successfully proven on different coinage metals,
and the formation process, together with the fingerprints associated
with each reaction step, has been studied by combining scanning tunneling
microscopy, core-level spectroscopy, and density functional calculations.
In addition to the GNR’s chiral edge structure, the substantial
GNR lengths achieved and the low processing temperature required to
complete the reaction grant this reactant extremely interesting properties
for potential applications.
On-surface covalent self-assembly of organic molecules is a very promising bottom–up approach for producing atomically controlled nanostructures. Due to their highly tuneable properties, these structures may be used as building blocks in electronic carbon-based molecular devices. Following this idea, here we report on the electronic structure of an ordered array of poly(para-phenylene) nanowires produced by surface-catalysed dehalogenative reaction. By scanning tunnelling spectroscopy we follow the quantization of unoccupied molecular states as a function of oligomer length, with Fermi level crossing observed for long chains. Angle-resolved photoelectron spectroscopy reveals a quasi-1D valence band as well as a direct gap of 1.15 eV, as the conduction band is partially filled through adsorption on the surface. Tight-binding modelling and ab initio density functional theory calculations lead to a full description of the band structure, including the gap size and charge transfer mechanisms, highlighting a strong substrate–molecule interaction that drives the system into a metallic behaviour.
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