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石墨烯上的分子自组装。

Molecular self-assembly on graphene.

机构信息

Centre Énergie Matériaux Télécommunications, Institut national de la recherche scientifique, 1650 Boul. Lionel-Boulet, Varennes, QC, J3X 1S2, Canada.

出版信息

Small. 2014 Mar 26;10(6):1038-49. doi: 10.1002/smll.201301982. Epub 2013 Oct 24.

DOI:10.1002/smll.201301982
PMID:24155272
Abstract

The formation of ordered arrays of molecules via self-assembly is a rapid, scalable route towards the realization of nanoscale architectures with tailored properties. In recent years, graphene has emerged as an appealing substrate for molecular self-assembly in two dimensions. Here, the first five years of progress in supramolecular organization on graphene are reviewed. The self-assembly process can vary depending on the type of graphene employed: epitaxial graphene, grown in situ on a metal surface, and non-epitaxial graphene, transferred onto an arbitrary substrate, can have different effects on the final structure. On epitaxial graphene, the process is sensitive to the interaction between the graphene and the substrate on which it is grown. In the case of graphene that strongly interacts with its substrate, such as graphene/Ru(0001), the inhomogeneous adsorption landscape of the graphene moiré superlattice provides a unique opportunity for guiding molecular organization, since molecules experience spatially constrained diffusion and adsorption. On weaker-interacting epitaxial graphene films, and on non-epitaxial graphene transferred onto a host substrate, self-assembly leads to films similar to those obtained on graphite surfaces. The efficacy of a graphene layer for facilitating planar adsorption of aromatic molecules has been repeatedly demonstrated, indicating that it can be used to direct molecular adsorption, and therefore carrier transport, in a certain orientation, and suggesting that the use of transferred graphene may allow for predictible molecular self-assembly on a wide range of surfaces.

摘要

通过自组装形成有序分子排列是实现具有定制性质的纳米结构的快速、可扩展途径。近年来,石墨烯作为二维分子自组装的有吸引力的基底而出现。本文综述了在石墨烯上超分子组织的前五年进展。自组装过程可以根据所使用的石墨烯类型而有所不同:在金属表面原位生长的外延石墨烯和转移到任意基底上的非外延石墨烯,可能对最终结构产生不同的影响。在外延石墨烯上,该过程对外延石墨烯与基底之间的相互作用很敏感。在与基底强烈相互作用的情况下,如石墨烯/Ru(0001),石墨烯莫尔超晶格的不均匀吸附景观为指导分子组织提供了独特的机会,因为分子经历空间受限的扩散和吸附。在外延石墨烯薄膜较弱相互作用的情况下,以及转移到基底上的非外延石墨烯上,自组装导致类似于在石墨表面上获得的薄膜。石墨烯层促进芳香族分子平面吸附的功效已被反复证明,表明它可用于以特定取向引导分子吸附,从而引导载流子传输,这表明转移石墨烯的使用可能允许在广泛的表面上进行可预测的分子自组装。

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