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在石墨上取向排列的大尺寸六方氮化硼单晶的非催化异质外延生长。

Non-catalytic heteroepitaxial growth of aligned, large-sized hexagonal boron nitride single-crystals on graphite.

作者信息

Arai Hayato, Inoue Taiki, Xiang Rong, Maruyama Shigeo, Chiashi Shohei

机构信息

Department of Mechanical Engineering, The University of Tokyo, Tokyo 113-8656, Japan.

出版信息

Nanoscale. 2020 May 14;12(18):10399-10406. doi: 10.1039/d0nr00849d.

Abstract

Although van der Waals heterostructures composed of graphene and hexagonal boron nitride (h-BN) have attracted wide interest, it is still challenging to prepare them with high quality and controllability. Since contamination induced by transfer cannot be avoided in the case of growth on a metal catalyst, the non-catalytic growth of graphene and h-BN is highly desired. However, unlike graphene, few studies have reported the non-catalytic growth of h-BN, and the lack of controllability in terms of crystal orientation and nucleation density, and size of h-BN has hindered the practical applications of the heterostructures. In this work, we demonstrate the heteroepitaxial growth of aligned monolayer h-BN single-crystals on exfoliated graphite by chemical vapour deposition (CVD) without a metal catalyst. Triangular shaped domains were aligned with each other, which suggests the epitaxy between h-BN and the underlying graphite. Characterisation by Raman spectroscopy, Auger electron spectroscopy, and X-ray photoelectron spectroscopy also confirmed that the h-BN/graphite samples were of high quality. A growth kinetics study over different temperatures indicated an increase in the growth rate at high temperature. Control of nucleation density was realised by changing the hydrogen pressure during CVD or by the heating temperature in air before CVD. Under the optimised growth conditions, the edge length of h-BN single-crystals grew to ∼1 μm, which is the largest size to date for non-catalytic growth. These results will help to obtain structure-controlled, large-area, and impurity-free heterostructures based on h-BN and graphene.

摘要

尽管由石墨烯和六方氮化硼(h-BN)组成的范德华异质结构已引起广泛关注,但高质量且可控地制备它们仍然具有挑战性。由于在金属催化剂上生长时无法避免转移过程中引起的污染,因此非常需要石墨烯和h-BN的非催化生长。然而,与石墨烯不同,很少有研究报道h-BN的非催化生长,并且h-BN在晶体取向、成核密度和尺寸方面缺乏可控性,这阻碍了异质结构的实际应用。在这项工作中,我们展示了通过化学气相沉积(CVD)在剥离的石墨上无金属催化剂的情况下,取向排列的单层h-BN单晶的异质外延生长。三角形区域相互对齐,这表明h-BN与下层石墨之间存在外延关系。拉曼光谱、俄歇电子能谱和X射线光电子能谱表征也证实了h-BN/石墨样品的高质量。对不同温度下的生长动力学研究表明,高温下生长速率增加。通过在CVD过程中改变氢气压力或在CVD之前在空气中的加热温度来实现对成核密度的控制。在优化的生长条件下,h-BN单晶的边长增长到约1μm,这是迄今为止非催化生长的最大尺寸。这些结果将有助于获得基于h-BN和石墨烯的结构可控、大面积且无杂质的异质结构。

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