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arXiv physics/0702065physics.chem-ph
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模拟阳离子在水中选择性分配到带负电荷的纳米孔中

Modeling the selective partitioning of cations into negatively charged nanopores in water

Lu Yang, Shekhar Garde

摘要:

水和小溶质进入和通过纳米孔的分配和运输对于各种化学和生物过程和应用是重要的。在这里,我们研究分区的正离子的大小增加到孔隙内部使用广泛的分子动力学模拟。尽管简单的模拟系统,结果提供了新的和有用的见解的孔隙水化和离子分配。对于孔上的低负电荷密度,用于将正离子分配到孔中的驱动力是弱的,并且没有观察到分配。孔电荷逐渐增加导致正离子进入孔的分区。有趣的是,在一系列的中间负电荷密度,纳米孔显示出热力学以及动力学的选择性分配较大的K+和Cs+离子进入其内部的较小的Na+离子。热力学驱动力和平均分配时间随孔电荷密度的变化表明,在分配过程中存在自由能垒。我们讨论了离子水合作用在体和在孔内部,以及在确定离子分区和所观察到的热力学和动力学选择性的势垒高度的孔水合作用。

英文摘要:

Partitioning and transport of water and small solutes into and through nanopores is important to a variety of chemical and biological processes and applications. Here we study the partitioning of positive ions of increasing size into the pore interior using extensive molecular dynamics simulations. Despite the simplicity of the simulation system, the results provide new and useful insights on both the pore hydration and ion partitioning. For low negative charge densities on the pore, the driving force for partitioning of positive ions into the pore is weak, and no partitioning is observed. Increasing the pore charge gradually leads to partitioning of positive ions into the pore. Interestingly, over a range of intermediate negative charge densities, nanopores display both thermodynamic as well as kinetic selectivity toward partitioning of the larger K+ and Cs+ ions into their interior over the smaller Na+ ions. The variation of thermodynamic driving force and the average partitioning time with the pore charge density together suggest the presence of free energy barriers in the partitioning process. We discuss the role of ion hydration in the bulk and in the pore interior as well as of the pore hydration in determining the barrier heights for ion partitioning and the observed thermodynamic and kinetic selectivity.

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