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正交电场作用下狭窄疏水通道的浸润与去浸润:不同水模型的结构、自由能及动力学

Wetting and dewetting of narrow hydrophobic channels by orthogonal electric fields: Structure, free energy, and dynamics for different water models.

作者信息

Kayal Abhijit, Chandra Amalendu

机构信息

Department of Chemistry, Indian Institute of Technology, Kanpur 208016, India.

出版信息

J Chem Phys. 2015 Dec 14;143(22):224708. doi: 10.1063/1.4936939.

Abstract

Wetting and dewetting of a (6,6) carbon nanotube in presence of an orthogonal electric field of varying strengths are studied by means of molecular dynamics simulations using seven different models of water. We have looked at filling of the channel, occupancy and structure of water inside it, associated free energy profiles, and also dynamical properties like the time scales of collective dipole flipping and residence dynamics. For the current systems where the entire simulation box is under the electric field, the nanotube is found to undergo electrodrying, i.e., transition from filled to empty states on increase of the electric field. The free energy calculations show that the empty state is the most stable one at higher electric field as it raptures the hydrogen bond environment inside the carbon nanotube by reorienting water molecules to its direction leading to a depletion of water molecules inside the channel. We investigated the collective flipping of water dipoles inside the channel and found that it follows a fast stepwise mechanism. On the dynamical side, the dipole flipping is found to occur at a faster rate with increase of the electric field. Also, the rate of water flow is found to decrease dramatically as the field strength is increased. The residence time of water molecules inside the channel is also found to decrease with increasing electric field. Although the effects of electric field on different water models are found to be qualitatively similar, the quantitative details can be different for different models. In particular, the dynamics of water molecules inside the channel can vary significantly for different water models. However, the general behavior of wetting and dewetting transitions, enhanced dipole flips, and shorter residence times on application of an orthogonal electric field hold true for all water models considered in the current work.

摘要

利用七种不同的水模型,通过分子动力学模拟研究了在不同强度正交电场存在下(6,6)碳纳米管的润湿和去湿过程。我们研究了通道的填充情况、其中水的占有率和结构、相关的自由能分布,以及诸如集体偶极翻转的时间尺度和驻留动力学等动力学性质。对于当前整个模拟盒处于电场中的系统,发现碳纳米管会发生电干燥现象,即随着电场增强,从填充状态转变为空状态。自由能计算表明,在较高电场下空状态是最稳定的,因为它通过将水分子重新定向到其方向破坏了碳纳米管内部的氢键环境,导致通道内水分子的耗尽。我们研究了通道内水分子的集体翻转,发现它遵循快速的逐步机制。在动力学方面,发现随着电场增强,偶极翻转的速率加快。此外,随着场强增加,水流速率显著降低。通道内水分子的驻留时间也随着电场增加而减少。虽然发现电场对不同水模型的影响在定性上相似,但不同模型的定量细节可能不同。特别是,对于不同的水模型,通道内水分子的动力学可能有显著差异。然而,对于当前工作中考虑的所有水模型,在施加正交电场时润湿和去湿转变、增强的偶极翻转以及较短的驻留时间的一般行为都是成立的。

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