AI Article Synopsis

  • The study focuses on the detailed characterization of high-energy ball-milled molybdenum disulfide (2H-MoS) to evaluate its nanostructure and stacking properties.
  • An advanced analysis of X-ray powder diffraction patterns (XRPD) offers more precise insights into stacking degrees and estimates the presence of single-layer material, complemented by a new UV-Vis spectral approach to assess layer number and crystallite size.
  • Findings indicate that longer ball-milling leads to thinner stacks and smaller lateral sizes, with high-resolution transmission electron microscopy revealing defects that other methods may miss.

Article Abstract

As a case study for the evaluation of the nanostructure of layered materials, we report on results of the comprehensive characterization of high-energy ball-milled layered molybdenum disulfide (2H-MoS) on different length scales. Analysis of X-ray powder diffraction patterns (XRPDs) including the Debye background at low scattering angles caused by uncorrelated single or few-layer MoS slabs (full scattering model), yield much more precise data about the average stacking degree than routine XRPD evaluation, and an estimation of the amount of single layer material is possible. Reflections with super Lorentzian line shape can be satisfactorily modeled assuming different stacking sequences induced by the mechanical forces exerted during the high-energy ball-mill process. An advanced analysis of UV-Vis spectra to determine layer number and lateral crystallite size, which was recently developed for liquid exfoliation materials, is used for the first time, and the results demonstrate the universal applicability of the approach. The data obtained with this analysis support the main findings of evaluation of the XRPD data. Both methods clearly evidence that increasing the duration of high-energy ball-mill treatment leads to an increase of material with decreasing average stacking and a reduction of the lateral size of the slabs. Finally, high-resolution transmission electron microscopy enabled identification of defects which can hardly be detected in XRPDs or in UV-Vis spectra.

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Source
http://dx.doi.org/10.1039/c8nr07287fDOI Listing

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