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氮掺杂多孔石墨烯纳米带的自下而上合成

Bottom-up Synthesis of Nitrogen-Doped Porous Graphene Nanoribbons.

作者信息

Pawlak Rémy, Liu Xunshan, Ninova Silviya, D'Astolfo Philipp, Drechsel Carl, Sangtarash Sara, Häner Robert, Decurtins Silvio, Sadeghi Hatef, Lambert Colin J, Aschauer Ulrich, Liu Shi-Xia, Meyer Ernst

机构信息

University of Basel, Department of Physics, Klingelbergstrasse 82, Basel CH 4056, Switzerland.

Department of Chemistry and Biochemistry, University of Bern, Freiestrasse 3, Bern, CH 3012, Switzerland.

出版信息

J Am Chem Soc. 2020 Jul 22;142(29):12568-12573. doi: 10.1021/jacs.0c03946. Epub 2020 Jul 2.

Abstract

Although methods for a periodic perforation and heteroatom doping of graphene sheets have been developed, patterning closely spaced holes on the nanoscale in graphene nanoribbons is still a challenging task. In this work, nitrogen-doped porous graphene nanoribbons (N-GNRs) were synthesized on Ag(111) using a silver-assisted Ullmann polymerization of brominated tetrabenzophenazine. Insights into the hierarchical reaction pathways from single molecules toward the formation of one-dimensional organometallic complexes and N-GNRs are gained by a combination of scanning tunneling microscopy (STM), atomic force microscopy (AFM) with CO-tip, scanning tunneling spectroscopy (STS), and density functional theory (DFT).

摘要

尽管已经开发出了对石墨烯片进行周期性穿孔和杂原子掺杂的方法,但在石墨烯纳米带中以纳米尺度图案化紧密间隔的孔仍然是一项具有挑战性的任务。在这项工作中,使用溴化四苯并菲的银辅助乌尔曼聚合反应在Ag(111)上合成了氮掺杂多孔石墨烯纳米带(N-GNRs)。通过扫描隧道显微镜(STM)、带CO针尖的原子力显微镜(AFM)、扫描隧道谱(STS)和密度泛函理论(DFT)相结合的方法,深入了解了从单分子到形成一维有机金属配合物和N-GNRs的分级反应途径。

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