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使用四硫代钼酸根插层层状双氢氧化物作为前驱体制备单层二硫化钼的空间限制合成。

Space-confined synthesis of monolayer molybdenum disulfide using tetrathiomolybdate intercalated layered double hydroxide as precursor.

机构信息

Key Laboratory of Colloid and Interface Chemistry (Ministry for Education), Shandong University, Jinan 250100, PR China.

National Engineering Research Center for Colloidal Materials, Shandong University, Jinan 250100, PR China.

出版信息

J Colloid Interface Sci. 2019 Apr 1;541:183-191. doi: 10.1016/j.jcis.2019.01.079. Epub 2019 Jan 21.

Abstract

Monolayer molybdenum disulfide (M-MoS) nanosheets (NSs) have attracted tremendous attention owing to their extraordinary properties and extensive potential applications. However, the large-scale and cost-effective fabrication of uniform M-MoS NSs remains challenging. Herein, a novel space-confined synthesis strategy was developed for M-MoS NSs, using the interlayer spaces of layered double hydroxides (LDHs) as nanoreactors. The 2H-phase M-MoS NSs dispersed in water were obtained with a high production yield of ∼98.7%, a quite high monolayer ratio of ∼95%, a homogenous lateral size of ∼89 nm, and a large monodispersed concentration of ∼0.41 g L. The so-obtained M-MoS exhibits excellent electrocatalytic activity towards the hydrogen evolution reaction compared with bulk MoS. This work provides an effective route for large-scale fabrication of two-dimensional transition-metal dichalcogenide nanomaterials.

摘要

单层二硫化钼(M-MoS)纳米片(NSs)由于其非凡的性质和广泛的潜在应用而引起了极大的关注。然而,均匀的 M-MoS NSs 的大规模和具有成本效益的制造仍然具有挑战性。在此,开发了一种新的空间受限合成策略,使用层状双氢氧化物(LDHs)的层间空间作为纳米反应器来制备 M-MoS NSs。以高产率约 98.7%、相当高的单层比例约 95%、均匀的横向尺寸约 89nm 和大的单分散浓度约 0.41g/L 的方式,在水中获得了分散的 2H 相 M-MoS NSs。与体相 MoS 相比,所获得的 M-MoS 对析氢反应表现出优异的电催化活性。这项工作为二维过渡金属二卤化物纳米材料的大规模制造提供了一条有效途径。

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