Oh Jehyun, Park Minsuk, Kang Yoonbeen, Ju Sang-Yong
Department of Chemistry, Yonsei University, Seodaemun-Gu, Seoul 03722, Republic of Korea.
ACS Nano. 2024 Jul 23;18(29):19314-19323. doi: 10.1021/acsnano.4c05586. Epub 2024 Jul 13.
While the molten salt-catalyzed chemical vapor deposition (CVD) technique is recognized for its effectiveness in producing large-area transition metal chalcogenides, understanding their growth mechanisms involving alkali metals remains a challenge. Here, we investigate the kinetics and mechanism of sodium-catalyzed molybdenum disulfide (MoS) growth and etching through image analysis conducted using an integrated CVD microscope. Sodium droplets, agglomerated via the thermal decomposition of the sodium cholate dispersant, catalyze the precipitation of supersaturated MoS laminates and induce growth despite fragmentation during this process. Triangular MoS crystals display a distinct self-exhausting exponential behavior and slow growth of thermodynamically favorable crystallographic faces, exhibiting a sulfur-dominant pressure. The growth and etching processes are facilitated by the scooting of sodium droplets along grain edges, displaying comparable rates. Leveraging these kinetics makes it possible to engineer atypical MoS shapes. This combined microscope not only enhances the understanding of growth mechanisms but also contributes to the facile development of next-generation nanomaterials.
虽然熔盐催化化学气相沉积(CVD)技术因其在制备大面积过渡金属硫属化物方面的有效性而得到认可,但了解其涉及碱金属的生长机制仍然是一项挑战。在此,我们通过使用集成CVD显微镜进行图像分析,研究了钠催化二硫化钼(MoS)生长和蚀刻的动力学及机制。通过胆酸钠分散剂的热分解而团聚的钠滴,催化过饱和MoS层压板的沉淀,并在此过程中尽管发生破碎仍诱导生长。三角形MoS晶体呈现出独特的自耗尽指数行为以及热力学上有利的晶面的缓慢生长,表现出硫主导的压力。钠滴沿晶粒边缘的移动促进了生长和蚀刻过程,显示出相当的速率。利用这些动力学可以设计出非典型的MoS形状。这种组合显微镜不仅增强了对生长机制的理解,也有助于下一代纳米材料的便捷开发。