Dipartimento di Fisica, Universita' di Roma La Sapienza, Piazzale A. Moro 2, I-00185 Rome, Italy.
J Chem Phys. 2012 Sep 7;137(9):094908. doi: 10.1063/1.4749571.
Structure and dynamics of water confined in channels of diameter of few nanometer in size strongly differ from the ones of water in the bulk phase. Here, we present radiowave dielectric relaxation measurements on water-filled single-walled carbon nanotubes, with the aim of highlighting some aspects on the molecular electric dipole organization of water responding to high spatial confinement in a hydrophobic environment. The observed dielectric spectra, resulting into two contiguous relaxation processes, allow us to separate the confined water in the interior of the nanotubes from external water, providing support for the existence in the confinement region of water domains held together by hydrogen bonds. Our results, based on the deconvolution of the dielectric spectra due to the presence of a bulk and a confined water phase, furnish a significantly higher Kirkwood correlation factor, larger than the one of water in bulk phase, indicating a strong correlation between water molecules inside nanotubes, not seen in bulk water.
在直径只有几个纳米的通道中,水的结构和动力学与本体相中的水有很大的不同。在这里,我们展示了填充有水的单壁碳纳米管的无线电波介电弛豫测量结果,旨在突出在疏水环境中高空间限制下,水分子的分子电偶极组织的某些方面。观察到的介电谱,导致两个连续的弛豫过程,使我们能够将纳米管内部的束缚水与外部水分离,为在束缚区域中存在由氢键结合在一起的水域提供支持。我们的结果基于存在本体相和束缚水相的介电谱的解卷积,提供了一个明显更高的 Kirkwood 相关因子,大于本体相水中的相关因子,表明纳米管内水分子之间存在强烈的相关性,而在本体水中则没有观察到这种相关性。