Ruckhofer Adrian, Sacchi Marco, Payne Anthony, Jardine Andrew P, Ernst Wolfgang E, Avidor Nadav, Tamtögl Anton
Institute of Experimental Physics, Graz University of Technology, Graz, Austria.
Department of Chemistry, University of Surrey, Guildford GU2 7XH, UK.
Nanoscale Horiz. 2022 Oct 24;7(11):1388-1396. doi: 10.1039/d2nh00353h.
Large-area single-crystal monolayers of two-dimensional (2D) materials such as graphene and hexagonal boron nitride (h-BN) can be grown by chemical vapour deposition (CVD). However, the high temperatures and fast timescales at which the conversion from a gas-phase precursor to the 2D material appears, make it extremely challenging to simultaneously follow the atomic arrangements. We utilise helium atom scattering to discover and control the growth of novel 2D h-BN nanoporous phases during the CVD process. We find that prior to the formation of h-BN from the gas-phase precursor, a metastable (3 × 3) structure is formed, and that excess deposition on the resulting 2D h-BN leads to the emergence of a (3 × 4) structure. We illustrate that these nanoporous structures are produced by partial dehydrogenation and polymerisation of the borazine precursor upon adsorption. These steps are largely unexplored during the synthesis of 2D materials and we unveil the rich phases during CVD growth. Our results provide significant foundations for 2D materials engineering in CVD, by adjusting or carefully controlling the growth conditions and thus exploiting these intermediate structures for the synthesis of covalent self-assembled 2D networks.
诸如石墨烯和六方氮化硼(h-BN)等二维(2D)材料的大面积单晶单层可以通过化学气相沉积(CVD)生长。然而,从气相前驱体转化为二维材料所出现的高温和快速时间尺度,使得同时追踪原子排列极具挑战性。我们利用氦原子散射来发现和控制CVD过程中新型二维h-BN纳米多孔相的生长。我们发现,在从气相前驱体形成h-BN之前,会形成一种亚稳的(3×3)结构,并且在所得二维h-BN上的过量沉积会导致(3×4)结构的出现。我们表明,这些纳米多孔结构是由硼嗪前驱体在吸附时的部分脱氢和聚合产生的。在二维材料的合成过程中,这些步骤在很大程度上尚未被探索,并且我们揭示了CVD生长过程中的丰富相。我们的结果通过调整或仔细控制生长条件,从而利用这些中间结构来合成共价自组装二维网络,为CVD中的二维材料工程提供了重要基础。