Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, TN, 37831, USA.
Department of Mechanical and Nuclear Engineering, The Pennsylvania State University, University Park, PA, 16802, USA.
Nat Commun. 2018 Jun 11;9(1):2266. doi: 10.1038/s41467-018-04610-0.
Developing strategies for atomic-scale controlled synthesis of new two-dimensional (2D) functional materials will directly impact their applications. Here, using in situ aberration-corrected scanning transmission electron microscopy, we obtain direct insight into the homoepitaxial Frank-van der Merwe atomic layer growth mechanism of TiC single adlayers synthesized on surfaces of TiC MXene substrates with the substrate being the source material. Activated by thermal exposure and electron-beam irradiation, hexagonal TiC single adlayers form on defunctionalized surfaces of TiC MXene at temperatures above 500 °C, generating new 2D materials TiC and TiC. The growth mechanism for a single TiC adlayer and the energies that govern atom migration and diffusion are elucidated by comprehensive density functional theory and force-bias Monte Carlo/molecular dynamics simulations. This work could lead to the development of bottom-up synthesis methods using substrates terminated with similar hexagonal-metal surfaces, for controllable synthesis of larger-scale and higher quality single-layer transition metal carbides.
开发原子尺度控制合成新型二维(2D)功能材料的策略将直接影响它们的应用。在这里,我们使用原位像差校正扫描透射电子显微镜,直接观察到 TiC 单层自组装在 TiC MXene 衬底表面的范德瓦尔斯-弗兰克(Frank-van der Merwe)同质外延原子层生长机制,其中衬底作为源材料。在高于 500°C 的温度下,通过热暴露和电子束辐照,TiC 单层在 TiC MXene 的去功能化表面上形成,生成新的二维材料 TiC 和 TiC。通过综合密度泛函理论和力偏置蒙特卡罗/分子动力学模拟,阐明了单个 TiC 单层的生长机制以及控制原子迁移和扩散的能量。这项工作可能会导致使用具有类似六方金属表面的衬底的自下而上合成方法的发展,从而可控合成更大规模和更高质量的单层过渡金属碳化物。