Issue 43, 2017

Langmuir films and uniform, large area, transparent coatings of chemically exfoliated MoS2 single layers

Abstract

By manipulating colloidal dispersions of chemically exfoliated molybdenum disulfide (MoS2) into an appropriate spreading solvent, we demonstrate, for the first time, the ability to form stable, floating MoS2 Langmuir films without the use of surfactants or significant material loss into the aqueous sub-phase. While the floating sheets can be compressed into a densely tiled film by the barriers of a traditional Langmuir–Blodgett trough, we also report an edge-to-edge aggregation and spreading driven densification phenomena that allows the film to be built up from the outside of the trough inwards during the deposition process. Continued deposition allows us to fill the entire trough with a dense (85–95% coverage) film of discretely tiled 1T MoS2 nanosheets and to coat substrates as large as 130 cm2. The transfer efficiency is found to be as high as 120 m2 of coated area per gram of deposited MoS2. Comparing the transfer efficiency to the theoretical specific surface area of MoS2 provides a method to estimate film thickness and exfoliation efficiency. Atomic force microscopy and optical absorption measurements are used to corroborate this estimate of 2.7 layers for the traditional n-butyllithium exfoliation method used. We demonstrate that the films can be built up layer-by-layer and investigate the optical and electrical properties of the films before and after conversion from the 1T to 2H polymorph.

Graphical abstract: Langmuir films and uniform, large area, transparent coatings of chemically exfoliated MoS2 single layers

  • This article is part of the themed collection: 2D Materials

Supplementary files

Article information

Article type
Paper
Submitted
13 6 2017
Accepted
17 7 2017
First published
17 7 2017

J. Mater. Chem. C, 2017,5, 11275-11287

Langmuir films and uniform, large area, transparent coatings of chemically exfoliated MoS2 single layers

Y. Zhang, L. Xu, W. R. Walker, C. M. Tittle, C. J. Backhouse and M. A. Pope, J. Mater. Chem. C, 2017, 5, 11275 DOI: 10.1039/C7TC02637D

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