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范德华固体在晶格导向滑动过程中的摩擦。

Friction between van der Waals Solids during Lattice Directed Sliding.

机构信息

U.S. Naval Research Laboratory, Code 6177, Washington, DC 20375, United States.

Department of Chemistry and Chemical Biology, Harvard University , Cambridge, Massachusetts 02138, United States.

出版信息

Nano Lett. 2017 Jul 12;17(7):4116-4121. doi: 10.1021/acs.nanolett.7b00871. Epub 2017 Jun 9.

Abstract

Nanometer-scale crystals of the two-dimensional oxide molybdenum trioxide (MoO) were formed atop the transition metal dichalcogenides MoS and MoSe. The MoO nanocrystals are partially commensurate with the dichalcogenide substrates, being aligned only along one of the substrate's crystallographic axes. These nanocrystals can be slid only along the aligned direction and maintain their alignment with the substrate during motion. Using an AFM probe to oscillate the nanocrystals, it was found that the lateral force required to move them increased linearly with nanocrystal area. The slope of this curve, the interfacial shear strength, was significantly lower than for macroscale systems. It also depended strongly on the duration and the velocity of sliding of the crystal, suggesting a thermal activation model for the system. Finally, it was found that lower commensuration between the nanocrystal and the substrate increased the interfacial shear, a trend opposite that predicted theoretically.

摘要

二维氧化物三氧化钼(MoO)的纳米级晶体在过渡金属二硫化物 MoS 和 MoSe 上形成。MoO 纳米晶体与二硫化物衬底部分共格,仅沿着衬底的一个晶轴取向。这些纳米晶体只能沿着取向方向滑动,并在运动过程中保持与衬底的取向一致。使用原子力显微镜探针来振荡纳米晶体,发现移动它们所需的侧向力与纳米晶体的面积呈线性增加。该曲线的斜率,即界面剪切强度,明显低于宏观系统。它还强烈依赖于晶体滑动的持续时间和速度,这表明该系统的热激活模型。最后,发现纳米晶体与衬底之间的共格程度越低,界面剪切强度越高,这与理论预测的趋势相反。

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