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Universal Oriented van der Waals Epitaxy of 1D Cyanide Chains on Hexagonal 2D Crystals

机译:六角形二维晶体上一维氰化物链的万向取向范德华外延

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摘要

The atomic or molecular assembly on 2D materials through the relatively weak van der Waals interaction is quite different from the conventional heteroepitaxy and may result in unique growth behaviors. Here, it is shown that straight 1D cyanide chains display universal epitaxy on hexagonal 2D materials. A universal oriented assembly of cyanide crystals (AgCN, AuCN, and Cu Au CN) is observed, where the chains are aligned along the three zigzag lattice directions of various 2D hexagonal crystals (graphene, h‐BN, WS , MoS , WSe , MoSe , and MoTe ). The potential energy landscape of the hexagonal lattice induces this preferred alignment of 1D chains along the zigzag lattice directions, regardless of the lattice parameter and surface elements as demonstrated by first‐principles calculations and parameterized surface potential calculations. Furthermore, the oriented microwires can serve as crystal orientation markers, and stacking‐angle‐controlled vertical 2D heterostructures are successfully fabricated by using them as markers. The oriented van der Waals epitaxy can be generalized to any hexagonal 2D crystals and will serve as a unique growth process to form crystals with orientations along the zigzag directions by epitaxy.
机译:通过相对较弱的范德华相互作用,二维材料上的原子或分子组装与常规异质外延有很大不同,并且可能导致独特的生长行为。在此,表明直链一维氰化物链在六角形二维材料上显示通用外延。观察到一个通用取向的氰化物晶体组装体(AgCN,AuCN和Cu Au CN),其中链沿各种2D六角形晶体(石墨烯,h-BN,WS,MoS,WSe,MoSe的三个之字形晶格方向排列)和MoTe)。六边形晶格的势能态势导致沿锯齿形晶格方向的一维链的这种首选对齐方式,无论晶格参数和表面元素如何,如第一性原理计算和参数化的表面电势计算所示。此外,取向的微丝可以用作晶体取向标记,并且通过将它们用作标记成功地制造了堆叠角度控制的垂直二维异质结构。定向范德华外延可以推广到任何六边形2D晶体,并将作为独特的生长过程来形成通过外延沿锯齿形方向取向的晶体。

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