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Atomic-Scale Deformations at the Interface of a Mixed-Dimensional van der Waals Heterostructure

机译:在混合维范van der waals异质结构的界面处的原子尺度变形

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摘要

Molecular self-assembly due to chemical interactions is the basis of bottom-up nanofabrication, whereas weaker intermolecular forces dominate on the scale of macromolecules. Recent advances in synthesis and characterization have brought increasing attention to two and mixed-dimensional heterostructures, and it has been recognized that van der Waals (vdW) forces within the structure may have a significant impact on their morphology. Here, we suspend single-walled carbon nanotubes (SWCNTs) on graphene to create a model system for the study of a 1D-2D molecular interface through atomic-resolution scanning transmission electron microscopy observations. When brought into contact, the radial deformation of SWCNTs and the emergence of long-range linear grooves in graphene revealed by the three-dimensional reconstruction of the heterostructure are observed. These topographic features are strain-correlated but show no sensitivity to carbon nanotube helicity, electronic structure, or stacking order. Finally, despite the random deposition of the nanotubes, we show that the competition between strain and vdW forces results in aligned carbon carbon interfaces spanning hundreds of nanometers.
机译:由于化学相互作用的分子自组装是自下而上的纳米制作的基础,而弱分子间力占据巨大的大分子量表。合成和表征的最新进展使得越来越关注两个和混合尺寸异质结构,并且已经认识到该结构内的范德华(VDW)力可能对其形态产生显着影响。这里,我们在石墨烯上悬挂单壁碳纳米管(SWCNTS),以通过原子分辨率扫描透射电子显微镜观察来创建用于研究1D-2D分子界面的模​​型系统。当与接触接触时,观察到SWCNT的径向变形以及石墨烯中的长距离线性凹槽的出现通过异质结构的三维重建显示。这些地形特征是应变相关的,但对碳纳米管螺旋,电子结构或堆叠顺序没有敏感性。最后,尽管纳米管的随机沉积,但我们表明应变和VDW力之间的竞争导致跨越数百纳米的对齐碳碳接口。

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