材料科学
成核
六方氮化硼
单层
化学工程
硼
氮化硼
纳米技术
基质(水族馆)
双层
结晶学
石墨烯
化学
膜
有机化学
工程类
地质学
海洋学
生物化学
作者
Ying Hao,Xiuting Li,Deshuai Li,Mingqiang Huang,Wen Wan,Qian Yao,Xiangping Chen,Zhiwei Wang,Yanqing Wu,Le Wang,Shanshan Chen
出处
期刊:2D materials
[IOP Publishing]
日期:2018-03-20
卷期号:5 (2): 025020-025020
被引量:13
标识
DOI:10.1088/2053-1583/aab407
摘要
The scalable synthesis of two-dimensional (2D) hexagonal boron nitride (h-BN) is of great interest for its numerous applications in novel electronic devices. Highly-crystalline h-BN films, with single-crystal sizes up to hundreds of microns, are demonstrated via a novel Ni foam assisted technique reported here for the first time. The nucleation density of h-BN domains can be significantly reduced due to the high boron solubility, as well as the large specific surface area of the Ni foam. The crystalline structure of the h-BN domains is found to be well aligned with, and therefore strongly dependent upon, the underlying Pt lattice orientation. Growth-time dependent experiments confirm the presence of a surface mediated self-limiting growth mechanism for monolayer h-BN on the Pt substrate. However, utilizing remote catalysis from the Ni foam, bilayer h-BN films can be synthesized breaking the self-limiting effect. This work provides further understanding of the mechanisms involved in the growth of h-BN and proposes a facile synthesis technique that may be applied to further applications in which control over the crystal alignment, and the numbers of layers is crucial.
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