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在液-液界面室温制备纳米晶二硫化钼(MoS)

Room-Temperature Production of Nanocrystalline Molybdenum Disulfide (MoS) at the Liquid-Liquid Interface.

作者信息

Higgins Eliott P C, McAdams Simon G, Hopkinson David G, Byrne Conor, Walton Alex S, Lewis David J, Dryfe Robert A W

机构信息

National Graphene Institute, School of Chemistry, School of Materials, and Photon Science Institute, University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom.

出版信息

Chem Mater. 2019 Aug 13;31(15):5384-5391. doi: 10.1021/acs.chemmater.8b05232. Epub 2019 Jul 18.

Abstract

Scalable synthesis of 2D materials is a prerequisite for their commercial exploitation. Here, a novel method of producing nanocrystalline molybdenum disulfide (MoS) at the liquid-liquid interface is demonstrated by decomposing a molecular precursor (tetrakis(diethyldithiocarbamato) molybdenum(IV)) in an organic solvent. The decomposition occurs over a few hours at room temperature without stirring or the addition of any surfactants, producing MoS which can be isolated onto substrates of choice. The formation of MoS at the liquid-liquid interface can be accelerated by the inclusion of hydroxide ions in the aqueous phase, which we propose to act as a catalyst. The precursor concentration was varied to minimize MoS thickness, and the organic solvent was chosen to optimize the speed and quality of formation. The kinetics of the MoS formation has been investigated, and a reaction mechanism has been proposed. The synthesis method is, to the best of our knowledge, the first reported room-temperature synthesis of transition-metal dichalcogenides, offering a potential solution to scalable 2D material production.

摘要

二维材料的可扩展合成是其商业开发的前提条件。在此,通过在有机溶剂中分解分子前驱体(四(二乙基二硫代氨基甲酰基)钼(IV)),展示了一种在液-液界面制备纳米晶二硫化钼(MoS)的新方法。分解在室温下无需搅拌或添加任何表面活性剂的情况下进行数小时,生成的MoS可分离到选定的基底上。通过在水相中加入氢氧根离子可加速MoS在液-液界面的形成,我们认为氢氧根离子起到了催化剂的作用。改变前驱体浓度以最小化MoS的厚度,并选择有机溶剂以优化形成速度和质量。研究了MoS形成的动力学,并提出了反应机理。据我们所知,该合成方法是首次报道的室温合成过渡金属二硫属化物,为二维材料的可扩展生产提供了一种潜在的解决方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/babc/7011726/64d06bda9282/cm8b05232_0007.jpg

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