离子键合
整改
离子
纳米孔
离子流
选择性
化学物理
锥面
极化(电化学)
分析化学(期刊)
材料科学
化学
二极管
配体锥角
浓差极化
分子物理学
纳米技术
光电子学
膜
物理
热力学
物理化学
色谱法
有机化学
复合材料
功率(物理)
生物化学
催化作用
作者
Feibin Xiang,Wenchang Zhang,Xiaonan Yang,Shengfa Liang
标识
DOI:10.1021/acs.jpcb.1c10017
摘要
Originating from the ionic concentration polarization, ionic current rectification (ICR) is closely related to ion selectivity. Since it is the region with the greatest selectivity, the tip of the conical nanopore became the focus of research. However, even if the characteristic of the tip is fixed, the changes of pore length and cone angle still affect the magnitude of ICR─rectification factor (RF). This shows that only focusing on the selectivity of the tip is not comprehensive. Through the simulations based on the one-dimensional Poisson-Nernst-Planck model, it is found that the pore length and cone angle can influence the RF by changing the Dukhin number of pore base (Dubase). Here, Du is a parameter describing the ratio of excess ion concentration and bulk ion concentration. In addition, it is proved that the RF is determined by Dutip (Du of the pore tip) and Dubase together. On the basis of the results, we suggest that a uniformly charged conical nanopore can be equivalent to the series connection of many ultrashort nanochannels with different Du. The differences in Du between adjacent channels lead to unbalanced ion transport, ultimately leading to enrichment or depletion of ion concentration under different polarities. Besides, ICR in bipolar diodes also exhibits Du dependence. We anticipate that this work will provide help to understand the mechanism behind ICR.
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