化学物理
电解质
离子
材料科学
分子动力学
纳米技术
密闭空间
纳米尺度
同种类的
润湿
结构化
水溶液
化学
物理
电极
热力学
计算化学
物理化学
复合材料
经济
有机化学
财务
标识
DOI:10.1021/acs.jpclett.9b02139
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI