| Literature DB >> 36163268 |
James Lawrence1,2, Alejandro Berdonces-Layunta1,2, Shayan Edalatmanesh3, Jesús Castro-Esteban4, Tao Wang1,2, Alejandro Jimenez-Martin3,5,6, Bruno de la Torre3,5, Rodrigo Castrillo-Bodero2, Paula Angulo-Portugal2, Mohammed S G Mohammed1,2, Adam Matěj3,5, Manuel Vilas-Varela4, Frederik Schiller1,2, Martina Corso1,2, Pavel Jelinek7,8, Diego Peña9, Dimas G de Oteyza10,11,12,13.
Abstract
Carbon nanostructures with zigzag edges exhibit unique properties-such as localized electronic states and spins-with exciting potential applications. Such nanostructures however are generally synthesized under vacuum because their zigzag edges are unstable under ambient conditions: a barrier that must be surmounted to achieve their scalable integration into devices for practical purposes. Here we show two chemical protection/deprotection strategies, demonstrated on labile, air-sensitive chiral graphene nanoribbons. Upon hydrogenation, the chiral graphene nanoribbons survive exposure to air, after which they are easily converted back to their original structure by annealing. We also approach the problem from another angle by synthesizing a form of the chiral graphene nanoribbons that is functionalized with ketone side groups. This oxidized form is chemically stable and can be converted to the pristine hydrocarbon form by hydrogenation and annealing. In both cases, the deprotected chiral graphene nanoribbons regain electronic properties similar to those of the pristine nanoribbons. We believe both approaches may be extended to other graphene nanoribbons and carbon-based nanostructures.Entities:
Year: 2022 PMID: 36163268 DOI: 10.1038/s41557-022-01042-8
Source DB: PubMed Journal: Nat Chem ISSN: 1755-4330 Impact factor: 24.274