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On the equilibrium contact angle of sessile liquid drops from molecular dynamics simulations

机译:关于分子动力学模拟的术术液滴的平衡接触角

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We present a new methodology to estimate the contact angles of sessile drops from molecular simulations by using the Gaussian convolution method of Willard and Chandler [J. Phys. Chem. B 114, 1954-1958 (2010)] to calculate the coarse-grained density from atomic coordinates. The iso-density contour with average coarse-grained density value equal to half of the bulk liquid density is identified as the average liquid-vapor (LV) interface. Angles between the unit normal vectors to the average LV interface and unit normal vector to the solid surface, as a function of the distance normal to the solid surface, are calculated. The cosines of these angles are extrapolated to the three-phase contact line to estimate the sessile drop contact angle. The proposed methodology, which is relatively easy to implement, is systematically applied to three systems: (i) a Lennard-Jones (LJ) drop on a featureless LJ 9-3 surface; (ii) an SPC/E water drop on a featureless LJ 9-3 surface; and (iii) an SPC/E water drop on a graphite surface. The sessile drop contact angles estimated with our methodology for the first two systems are shown to be in good agreement with the angles predicted from Young's equation. The interfacial tensions required for this equation are computed by employing the test-area perturbation method for the corresponding planar interfaces. Our findings suggest that the widely adopted spherical-cap approximation should be used with caution, as it could take a long time for a sessile drop to relax to a spherical shape, of the order of 100 ns, especially for water molecules initiated in a lattice configuration on a solid surface. But even though a water drop can take a long time to reach the spherical shape, we find that the contact angle is well established much faster and the drop evolves toward the spherical shape following a constant-contact-angle relaxation dynamics. Making use of this observation, our methodology allows a good estimation of the sessile drop contact ang
机译:我们提出了一种新方法来估计通过使用威拉德和钱德勒的高斯卷积法从分子模拟中估计术中的接触角[J.物理。化学。 B 114,1954-1958(2010)]计算原子坐标的粗粒粒度密度。具有平均粗粒浓度的等值轮廓等于散装液体密度的一半的粗粒浓度值被鉴定为平均液体 - 蒸气(LV)界面。计算到平均LV接口的单位正常界面和单位正常矢量与固体表面的函数的角度,以正常到固体表面的函数。这些角度的余弦被推断为三相接触线以估计无梗塞接触角。所提出的方法是相对容易实现的,系统地应用于三个系统:(i)在无特色LJ 9-3表面上的Lennard-Jones(LJ)掉落; (ii)无特色LJ 9-3表面上的SPC / E水滴; (iii)石墨表面上的SPC / E水滴。与我们的前两个系统的方法估计的术语掉落接触角估计,与年轻方程的预测的角度达成良好。通过采用相应的平面界面的测试区域扰动方法来计算该等式所需的界面张力。我们的研究结果表明,广泛采用的球形帽近似应谨慎使用,因为它可能需要很长时间才能放松到球形的球形,尤其是在格子中发起的水分子在实心表面上配置。但即使水滴可能需要很长时间才能达到球形形状,我们发现接触角度很快,并且在恒定接触角松弛动态之后,下降朝向球形形状发展。利用这种观察,我们的方法允许良好地估计无柄液滴接触

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