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Unidirectional molecular assembly alignment on graphene enabled by nanomechanical symmetry breaking

机译:通过纳米力学对称性断裂实现石墨烯上的单向分子组装排列

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摘要

Precise fabrication of molecular assemblies on a solid surface has long been of central interest in surface science. Their perfectly oriented growth only along a desired in-plane direction, however, remains a challenge, because of the thermodynamical equivalence of multiple axis directions on a solid-surface lattice. Here we demonstrate the successful fabrication of an in-plane, unidirectional molecular assembly on graphene. Our methodology relies on nanomechanical symmetry breaking effects under atomic force microscopy tip scanning, which has never been used in molecular alignment. Individual one-dimensional (1D) molecular assemblies were aligned along a selected symmetry axis of the graphene lattice under finely-tuned scanning conditions after removing initially-adsorbed molecules. Experimental statistics and computational simulations suggest that the anisotropic tip scanning locally breaks the directional equivalence of the graphene surface, which enables nucleation of the unidirectional 1D assemblies. Our findings will open new opportunities in the molecular alignment control on various atomically flat surfaces.
机译:长期以来,在固体表面上精确组装分子组件一直是表面科学的主要兴趣所在。然而,由于在固体表面晶格上多轴方向的热力学等价性,它们仅沿期望的面内方向的完美定向生长仍然是一个挑战。在这里,我们演示了在石墨烯上成功制作面内,单向分子组装体的过程。我们的方法依赖于原子力显微镜尖端扫描下的纳米力学对称性断裂效应,该效应从未用于分子比对。去除初始吸附的分子后,在微调的扫描条件下,沿石墨烯晶格的选定对称轴排列各个一维(1D)分子组件。实验统计和计算模拟表明,各向异性尖端扫描会局部破坏石墨烯表面的方向等效性,从而使单向一维组件成核。我们的发现将为在各种原子平面上的分子排列控制提供新的机会。

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