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首页> 外文期刊>Nano letters >Liquids with Lower Wettability Can Exhibit Higher Friction on Hexagonal Boron Nitride: The Intriguing Role of Solid-Liquid Electrostatic Interactions
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Liquids with Lower Wettability Can Exhibit Higher Friction on Hexagonal Boron Nitride: The Intriguing Role of Solid-Liquid Electrostatic Interactions

机译:具有较低润湿性的液体可以在六边形氮化物上表现出更高的摩擦:固液静电相互作用的有趣作用

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We investigate the wetting and frictional behavior of polar (water and ethylene glycol) and nonpolar (diiodomethane) liquids on the basal plane of hexagonal boron nitride (hBN) using molecular dynamics simulations. Our results for the wettability of water on the hBN basal plane (contact angle 81 degrees) are in qualitative agreement with the experimentally deduced mild hydrophilicity of the hBN basal plane (contact angle 66 degrees). We find that water exhibits the lowest wettability, as quantified by the highest contact angle, but the highest friction coefficient of (1.9 +/- 0.4) x 10(5) N-s/m(3) on the hBN basal plane among the three liquids considered. This intriguing finding is explained in terms of the competition between dispersion and electrostatic interactions operating between the hBN basal plane and the three liquids. We find that electrostatic interactions do not affect the wetting behavior appreciably, as quantified by a less than 3 degrees change in the respective contact angles of the three liquids considered. On the other hand, electrostatic interactions are found to increase the friction coefficients of the three liquids in contact with hBN to different extents, indicating that despite the increased friction of water on hBN, relative to that on graphene, nonpolar liquids may exhibit similar friction coefficients on hBN and graphene. Our findings reveal that the increase in the friction coefficient, upon incorporation of solid-liquid electrostatic interactions, is brought about by a greater increase in the solid-liquid mean-squared total lateral force, as compared to a smaller reduction in the decorrelation time of the solid-liquid force.
机译:我们使用分子动力学模拟研究了使用分子动力学模拟的极性(水和乙二醇)和非极性(二碘甲烷)液体对六边形氮化物(HBN)的基础平面的润湿和摩擦行为。我们对HBN基础平面(接触角81度)上的水润湿性的结果与实验推导的HBN基底平面(接触角66度)的温和亲水性进行定性协议。我们发现水表现出最低的润湿性,通过最高的接触角来量化,但是三种液体中HBN基底平面上的(1.9 +/- 0.4)×10(5)ns / m(3)的最高摩擦系数经过考虑的。在HBN基底平面和三种液体之间运行的色散和静电相互作用之间的竞争来解释这种有趣的发现。我们发现静电相互作用不会显着影响润湿行为,如所考虑的三种液体的相应接触角的相应接触角度的量化量小于3度。另一方面,发现静电相互作用将三个液体与HBN接触的摩擦系数增加到不同的范围,表明尽管HBN上的水摩擦增加,相对于石墨烯,但非极性液体可能表现出类似的摩擦系数在HBN和石墨烯上。我们的发现表明,在掺入固体型静电相互作用时,摩擦系数的增加由固体均匀的全侧向的较大增加,与较小的去相关时间的减少相比固液力。

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