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Electrolytes under Inhomogeneous Nanoconfinement: Water Structuring-Mediated Local Ion Accumulation

机译:非均匀纳米序列下的电解质:水结构介导的局部离子积聚

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The behaviors of aqueous electrolytes confined in nanoscale spaces impact a broad range of biological processes and industrial applications. Our current microscopic understanding of confined electrolytes relies primarily on ideal model systems featuring homogeneous nanoconfinement. Here, we investigate the structure and dynamics of various electrolytes subject to inhomogeneous nanoconfinement, i.e., confined in two-dimensional nanochannels with gradually varying local channel heights, by means of molecular dynamics simulations. Our results reveal unexpected local ion accumulation in the inhomogeneous space occurring at boundaries between coexisting structured water phases, including trilayer, four-layer, and bulk-like waters. This contrasts markedly with the intuition that hydrated ions are more favorable to weakly confined regimes due to a steric exclusion effect. We further show that the location and intensity of the water structuring-mediated ion accumulation are sensitive to the nanochannel's geometry and surface wettability. The revealed anomalous ion behaviors in inhomogeneous nanoconfinement should help to improve our understanding of the microscopic mechanism underlying the operation of biological ion channels and to develop functional nanofluidic devices.
机译:纳米级空间内限制的水性电解质的行为影响了广泛的生物方法和工业应用。我们目前对受限电解质的显微镜理解主要依赖于具有均匀纳米纯净的理想模型系统。在这里,我们研究了通过分子动力学模拟逐渐变化的局部通道高度的两维纳米纳米镍的各种电解质的结构和动力学。我们的结果揭示了在共存结构水相之间发生的非均匀空间中的意外的局部离子积聚,包括三层,四层和散装水。由于由于空间排除效应,水合离子更有利于水合离子更有利地对比。我们进一步表明,水结构介导的离子积聚的位置和强度对纳米通道的几何形状和表面润湿性敏感。非均匀纳米核的揭示的异常离子行为应该有助于改善我们对生物离子通道操作的微观机制的理解,并开发功能性纳米流体装置。

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