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Estimation of interaction energy and contact stiffness in atomic-scale sliding on a model sodium chloride surface in ethanol

机译:乙醇中模型氯化钠表面上原子级滑动的相互作用能和接触刚度的估计

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摘要

Friction force microscopy (FFM) in aqueous environments has recently proven to be a very effective method for lattice-resolution imaging of crystal surfaces. Here we demonstrate the use of ethanol for similar measurements on water-soluble materials. Lattice resolved frictional stick-slip traces of a cleaved NaCl(100) surface submerged in ethanol are compared with previous obtained FFM results in ultrahigh vacuum (UHV). We use the Prandtl-Tomlinson framework to estimate the amplitude of the corrugation potential and the contact stiffness. The surface potential amplitude scales with the applied normal loads are in good agreement with data obtained for NaCl measured under UHV conditions, but demonstrates deviations from the ideal periodic potential given by the Prandtl-Tomlinson model. An additional finding is that the use of ethanol allows us to explore higher load ranges without detectable evidence of surface wear. The contact stiffness does not vary significantly with the normal load up to 38 nN, while above it a sudden increase by almost one order of magnitude was observed. Comparing this to previous results suggests that considerable atom rearrangements may occur in the contact region, although the (100) surface structure is preserved by ethanol-assisted diffusion of Na and Cl ions.
机译:最近已证明,在水性环境中使用摩擦力显微镜(FFM)是对晶体表面进行晶格分辨率成像的一种非常有效的方法。在这里,我们演示了使用乙醇对水溶性材料进行类似测量。在超高真空度(UHV)中,将浸没在乙醇中的NaCl(100)裂解表面的晶格分辨摩擦粘滑痕迹与先前获得的FFM结果进行比较。我们使用Prandtl-Tomlinson框架来估计波纹势的振幅和接触刚度。具有施加的法向载荷的表面电势振幅标度与在特高压条件下测量的NaCl数据非常吻合,但表明与Prandtl-Tomlinson模型给出的理想周期性电势存在偏差。另一个发现是乙醇的使用使我们能够探索更高的负载范围,而没有可检测到的表面磨损迹象。在最高38 nN的正常负载下,接触刚度并没有显着变化,而在此之上,观察到突然增加了近一个数量级。将其与先前的结果进行比较表明,尽管(100)表面结构通过乙醇辅助的Na和Cl离子扩散得以保留,但在接触区域中可能发生相当大的原子重排。

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