Liu Chenze, Lin Yu-Chuan, Yoon Mina, Yu Yiling, Puretzky Alexander A, Rouleau Christopher M, Chisholm Matthew F, Xiao Kai, Eres Gyula, Duscher Gerd, Geohegan David B
Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States.
Department of Materials Science and Engineering, University of Tennessee, Knoxville, Tennessee 37996, United States.
ACS Nano. 2021 May 25;15(5):8638-8652. doi: 10.1021/acsnano.1c00571. Epub 2021 Apr 30.
Understanding the bottom-up synthesis of atomically thin two-dimensional (2D) crystals and heterostructures is important for the development of new processing strategies to assemble 2D heterostructures with desired functional properties. Here, we utilize laser-heating within a transmission electron microscope (TEM) to understand the stages of crystallization and coalescence of amorphous precursors deposited by pulsed laser deposition (PLD) as they are guided by 2D crystalline substrates into van der Waals (vdW) epitaxial heterostructures. Amorphous clusters of tungsten selenide were deposited by PLD at room temperature onto graphene or MoSe monolayer crystals that were suspended on TEM grids. The precursors were then stepwise evolved into 2D heterostructures with pulsed laser heating treatments within the TEM. The lattice-matching provided by the MoSe substrate is shown to guide the formation of large-domain, heteroepitaxial vdW WSe/MoSe bilayers both during the crystallization process via direct templating and after crystallization by assisting the coalescence of nanosized domains through nonclassical particle attachment processes including domain rotation and grain boundary migration. The favorable energetics for domain rotation induced by lattice matching with the substrate were understood from first-principles calculations. These TEM studies of pulsed laser-driven nonequilibrium crystallization phenomena represent a transformational tool for the rapid exploration of synthesis and processing pathways that may occur on extremely different length and time scales and lend insight into the growth of 2D crystals by PLD and laser crystallization.
了解原子级薄的二维(2D)晶体和异质结构的自下而上合成对于开发新的加工策略以组装具有所需功能特性的2D异质结构至关重要。在这里,我们利用透射电子显微镜(TEM)内的激光加热来了解通过脉冲激光沉积(PLD)沉积的非晶前驱体的结晶和聚结阶段,因为它们在2D晶体衬底的引导下形成范德华(vdW)外延异质结构。室温下通过PLD将硒化钨的非晶团簇沉积到悬浮在TEM网格上的石墨烯或MoSe单层晶体上。然后通过TEM内的脉冲激光加热处理将前驱体逐步演变成2D异质结构。结果表明,MoSe衬底提供的晶格匹配在结晶过程中通过直接模板作用引导大尺寸异质外延vdW WSe/MoSe双层的形成,并在结晶后通过包括畴旋转和晶界迁移在内的非经典粒子附着过程协助纳米尺寸畴的聚结。通过第一性原理计算理解了与衬底晶格匹配引起的畴旋转的有利能量学。这些关于脉冲激光驱动的非平衡结晶现象的TEM研究代表了一种变革性工具,用于快速探索可能在极不同的长度和时间尺度上发生的合成和加工途径,并深入了解通过PLD和激光结晶生长2D晶体的过程。