Park Junmo, Bong Sungmin, Park Jaehyun, Lee Eunji, Ju Sang-Yong
Department of Chemistry, Yonsei University, 50 Yonsei-ro, Seodaemun-Gu, Seoul 03722, Republic of Korea.
School of Materials Science and Engineering, Gwangju Institute of Science and Technology, 123 Cheomdangwagi-ro, Buk-gu, Gwangju 61005, Republic of Korea.
ACS Appl Mater Interfaces. 2022 Oct 26. doi: 10.1021/acsami.2c12592.
Although various methods have been developed to disperse transition metal dichalcogenides (TMDCs) in aqueous environments, the methodology to generate stable TMDC dispersions remains challenging. Here, we developed a hierarchical van der Waals (vdW) heterostructure-based strategy to disperse few-layered TMDCs (WS, MoS, WSe, and MoSe) using both hexagonal boron nitride (hBN) and sodium cholate (SC) as synergistic vdW surfactants. By showing long-term stability of up to 3 years, the extinction spectra of these TMDC/hBN/SC dispersions exhibit the most blue-shifted excitonic transitions, low background extinction, good colloidal stability, and dispersion stability upon ultracentrifugation compared to other dispersion methods. Hierarchical stacking having TMDCs and hBN/SC as core and shell parts is probed by electrostatic/atomic force microscopy and zeta potential, and its origin was attributed to surface energy matches. Along with the synergetic effect between TMDCs and hBN, the blue shift was ascribed to compressive strain on the TMDCs caused by hBN wrapping. The results of transmission electron microscopy show that the TMDCs in the dispersions have defective, few-layered structures with flake sizes that are less than a few hundred nm. Raman spectroscopy is used to study not only the existence of compressive strain but also various interlayer coupling between TMDC and hBN. The hierarchical structures of TMDC/hBN/SC are discussed in terms of surface energies and topographies. This method is invaluable to provide a general methodology to disperse various surface-corrugated dimensional materials for various dispersion-based applications.
尽管已经开发出各种方法来将过渡金属二卤化物(TMDCs)分散在水性环境中,但生成稳定的TMDC分散体的方法仍然具有挑战性。在这里,我们开发了一种基于分层范德华(vdW)异质结构的策略,使用六方氮化硼(hBN)和胆酸钠(SC)作为协同vdW表面活性剂来分散少层TMDCs(WS、MoS、WSe和MoSe)。通过显示长达3年的长期稳定性,与其他分散方法相比,这些TMDC/hBN/SC分散体的消光光谱表现出最大的蓝移激子跃迁、低背景消光、良好的胶体稳定性和超速离心后的分散稳定性。通过静电/原子力显微镜和zeta电位探测了以TMDCs和hBN/SC为核壳部分的分层堆叠,其起源归因于表面能匹配。除了TMDCs和hBN之间的协同效应外,蓝移归因于hBN包裹对TMDCs造成的压缩应变。透射电子显微镜结果表明,分散体中的TMDCs具有缺陷的少层结构,薄片尺寸小于几百纳米。拉曼光谱不仅用于研究压缩应变的存在,还用于研究TMDC和hBN之间的各种层间耦合。从表面能和形貌方面讨论了TMDC/hBN/SC的分层结构。该方法对于为各种基于分散的应用提供一种分散各种表面有波纹的尺寸材料的通用方法非常有价值。