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首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Comparative Study of Water-Mediated Interactions between Hydrophilic and Hydrophobic Nanoscale Surfaces
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Comparative Study of Water-Mediated Interactions between Hydrophilic and Hydrophobic Nanoscale Surfaces

机译:水中含水型纳米级表面水介导的相互作用的比较研究

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摘要

Self-assembly processes in aqueous solutions, such as protein folding and nanoparticle aggregation, are driven by water-mediated interactions (WMIs). The most common of such interactions are the attractive forces between hydrophobic units. While numerous studies have focused on hydrophobic interactions, WMIs between hydrophilic moieties and pairs of hydrophilic-hydrophobic surfaces have received much less attention. In this work, we perform molecular dynamics simulations to study the WMI between nanoscale (i) hydrophobic-hydrophobic, (ii) hydrophilic-hydrophilic, and (iii) hydrophilic-hydrophobic pairs of (hydroxylated/nonhydroxylated) graphene-based surfaces. We find that in all cases, the potential of mean force (PMF) between the plates exhibits oscillations as a function of the plate separations r, up to r approximate to 1-1.5 nm. The local minima of the PMF, which define the stable/metastable states of the system, correspond to plates' separations at which water molecules arrange into n = 0, 1, 2, ... layers between the plates. In case (i), the stable state of the system corresponds to the plates in contact with one another. Instead, in cases (ii) and (iii), water is never removed between the plates. The free-energy barriers separating the stable/metastable states of the system vary with the hydrophilicity/hydrophobicity of the interacting plates. However, the effective forces between the plates are comparable in magnitude. This strongly suggests that hydrophilic-hydrophilic and hydrophilic-hydrophobic interactions can play a relevant role in self-assembly processes in aqueous solutions, alike hydrophobic interactions. Interestingly, we find that the WMIs between hydrophilic-hydrophilic and hydrophilic-hydrophobic plates are similar, suggesting that only one hydrophilic surface is sufficient to induce hydrophilic-like WMI. We also briefly discuss the role of surface polarity on the WMI. In particular, we show that depending on the surface polarity, WMI can exhibit mixed features characteristic of hydrophobic and hydrophilic interactions. Our results suggest that the forces between hydrophobic, hydrophilic, and hydrophobic/hydrophilic surfaces are all relevant in driving a self-assembly system toward its final state, but it is the hydrophobic interaction that provides stability to such a final state.
机译:水溶液中的自组装过程,例如蛋白质折叠和纳米颗粒聚集,由水介导的相互作用(WMI)驱动。这种相互作用中最常见的是疏水单元之间的吸引力。虽然许多研究专注于疏水相互作用,但亲水性部分和亲水性 - 疏水表面的对的WMIs受到了更少的关注。在这项工作中,我们进行分子动力学模拟,以研究纳米级(I)疏水性 - 亲水性(II)亲水 - 亲水性的WMI和(III)亲水 - 疏水对(羟基化/非羟基化)石墨烯基表面。我们发现在所有情况下,板之间的平均力(PMF)的电位显示为板间分离R的函数,直至1-1.5nm。 PMF的局部最小值,其定义系统的稳定/亚稳态状态,对应于平板的分离,水分子在板之间布置在n = 0,1,2,...层。在(i)的情况下,系统的稳定状态对应于彼此接触的板。相反,在(ii)和(iii)中,从未在板之间移除水。分离系统的稳定/稳定状态的自由能屏障随着相互作用板的亲水性/疏水性而变化。然而,板之间的有效力量的幅度相当。这强烈表明,亲水亲水和亲水 - 疏水相互作用可以在水溶液中的自组装过程中发挥相关作用,相似疏水相互作用。有趣的是,我们发现亲水 - 亲水和亲水 - 疏水板之间的WMI是相似的,表明只有一种亲水性表面足以诱导亲水性的WMI。我们还简要介绍了表面极性对WMI的作用。特别地,我们表明,取决于表面极性,WMI可以表现出疏水性和亲水性相互作用的混合特征。我们的研究结果表明,疏水性,亲水和疏水性/亲水性表面之间的力在驱动自组装系统朝向其最终状态时都是相关的,但是疏水相互作用,其为这种最终状态提供稳定性。

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