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碳纳米管中温度对离子水合作用影响的分子模拟研究

Molecular simulation study of temperature effect on ionic hydration in carbon nanotubes.

作者信息

Shao Qing, Huang Liangliang, Zhou Jian, Lu Linghong, Zhang Luzheng, Lu Xiaohua, Jiang Shaoyi, Gubbins Keith E, Shen Wenfeng

机构信息

State Key Laboratory of Materials-oriented Chemical Engineering, Nanjing University of Technology, Nanjing 210009, China.

出版信息

Phys Chem Chem Phys. 2008 Apr 14;10(14):1896-906. doi: 10.1039/b719033f. Epub 2008 Feb 25.

Abstract

Molecular dynamics simulations have been performed to investigate the hydration of Li(+), Na(+), K(+), F(-), and Cl(-) inside the carbon nanotubes at temperatures ranging from 298 to 683 K. The structural characteristics of the coordination shells of ions are studied, including the ion-oxygen radial distribution functions, the coordination numbers, and the orientation distributions of the water molecules. Simulation results show that the first coordination shells of the five ions still exist in the nanoscale confinement. Nevertheless, the first coordination shell structures of cations change more significantly than those of anions because of the preferential orientation of the water molecules induced by the carbon nanotube. The first coordination shells of cations are considerably less ordered in the nanotube than in the bulk solution, whereas the change of the first coordination shell structures of the anions is minor. Furthermore, the confinement induces the anomalous behavior of the coordination shells of the ions with temperature. The first coordination shell of K(+) are found to be more ordered as the temperature increases only in the carbon nanotube with the effective diameter of 1.0 nm, implying the enhancement of the ionic hydration with temperature. This is contrary to that in the bulk solution. The coordination shells of the other four ions do not have such behavior in the carbon nanotube with the effective diameter ranging from 0.73 to 1.00 nm. The easier distortion of the coordination shell of K(+) and the match of the shell size and the nanotube size may play roles in this phenomenon. The exchange of water molecules in the first coordination shells of the ions with the solution and the ion diffusion along the axial direction of the nanotube are also investigated. The mobility of the ions and the stability of the coordination shells are greatly affected by the temperature in the nanotube as in the bulk solutions. These results help to understand the biological and chemical processes at the high temperature.

摘要

已进行分子动力学模拟,以研究在298至683 K温度范围内,碳纳米管内Li(+)、Na(+)、K(+)、F(-)和Cl(-)的水合作用。研究了离子配位壳的结构特征,包括离子-氧径向分布函数、配位数和水分子的取向分布。模拟结果表明,这五种离子的第一配位壳在纳米尺度限制下仍然存在。然而,由于碳纳米管诱导的水分子优先取向,阳离子的第一配位壳结构变化比阴离子更显著。阳离子的第一配位壳在纳米管中比在本体溶液中有序程度低得多,而阴离子的第一配位壳结构变化较小。此外,限制作用会导致离子配位壳随温度出现反常行为。仅在有效直径为1.0 nm的碳纳米管中,发现K(+)的第一配位壳随着温度升高而变得更有序,这意味着离子水合作用随温度增强。这与本体溶液中的情况相反。在有效直径为0.73至1.00 nm的碳纳米管中,其他四种离子的配位壳没有这种行为。K(+)配位壳更容易变形以及壳尺寸与纳米管尺寸的匹配可能在这一现象中起作用。还研究了离子第一配位壳中的水分子与溶液的交换以及离子沿纳米管轴向的扩散。与本体溶液一样,纳米管中的温度对离子迁移率和配位壳稳定性有很大影响。这些结果有助于理解高温下的生物和化学过程。

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