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单层水和异丙醇在二硫化钼纳米片之间的去湿现象。

Dewetting of monolayer water and isopropanol between MoS nanosheets.

作者信息

Wang Beibei, Kalia Rajiv K, Nakano Aiichiro, Vashishta Priya D

机构信息

Collaboratory of Advanced Computing and Simulations, University of Southern California, Los Angeles, USA.

Department of Physics and Astronomy, University of Southern California, Los Angeles, USA.

出版信息

Sci Rep. 2018 Nov 12;8(1):16704. doi: 10.1038/s41598-018-35163-3.

Abstract

Understanding dewetting of solvent molecules confined to layered material (LM) interfaces is crucial to the synthesis of two-dimensional materials by liquid-phase exfoliation. Here, we examine dewetting behavior of water and isopropanol/water (IPA/HO) mixtures between molybdenum disulfide (MoS) membranes using molecular dynamics (MD) simulations. We find that a monolayer of water spontaneously ruptures into nanodroplets surrounded by dry regions. The average speed of receding dry patches is close to the speed of sound in air. In contrast, monolayer mixtures of IPA/HO between MoS membranes slowly transform into percolating networks of nanoislands and nanochannels in which water molecules diffuse inside and IPA molecules stay at the periphery of islands and channels. These contrasting behaviors may explain why IPA/HO mixtures are much more effective than HO alone in weakening interlayer coupling and exfoliating MoS into atomically thin sheets.

摘要

了解限制在层状材料(LM)界面的溶剂分子的去湿对于通过液相剥离合成二维材料至关重要。在这里,我们使用分子动力学(MD)模拟研究了二硫化钼(MoS)膜之间水和异丙醇/水(IPA/H₂O)混合物的去湿行为。我们发现单层水会自发破裂成被干燥区域包围的纳米液滴。后退干燥斑块的平均速度接近空气中的声速。相比之下,MoS膜之间的IPA/H₂O单层混合物会缓慢转变为纳米岛和纳米通道的渗流网络,其中水分子在内部扩散,IPA分子则留在岛和通道的周边。这些截然不同的行为可能解释了为什么IPA/H₂O混合物在削弱层间耦合以及将MoS剥离成原子薄片方面比单独的H₂O有效得多。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e742/6232136/96a0abb74650/41598_2018_35163_Fig1_HTML.jpg

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