纳米流体学
化学物理
离子
离子键合
电导率
离子电导率
纳米技术
溶剂化
材料科学
石墨烯
离子液体
纳米尺度
离子运输机
分子动力学
电解质
导电体
电化学
化学
电极
计算化学
物理化学
复合材料
有机化学
催化作用
作者
Ke Zhou,Shuping Jiao,Yan Chen,Huasong Qin,Yilun Liu
出处
期刊:Langmuir
[American Chemical Society]
日期:2021-10-21
卷期号:37 (43): 12577-12585
被引量:8
标识
DOI:10.1021/acs.langmuir.1c01876
摘要
The ionic transport in nanoscale channels with the critical size comparable to ions and solvents shows excellent performance on electrochemical desalination, ion separation, and supercapacitors. However, the key quantity ionic conductivity (σ) in the nanochannel that evaluates how easily the electric current is driven by an external voltage is still unknown because of the challenges in experimental measurement. In this work, we present an atomistic simulation-based study, which shows that how the ion concentration, nanoconfinement, and heterogeneous solvation modify the ionic conductivity in a two-dimensional graphene nanochannel. We find that σ in the confined channel is lower than that in the bulk (σb) at the same concentration along with enhanced ion-ion correlation. However, surprisingly, the local σ near the channel wall is more conductive than σb and is about 2-3 folds of the inner layer due to the highly concentrated charge carriers. Based on the layered feature of σ along the width of the channel, we propose a model that contains two dead (or depletion) layers, two highly conductive layers, and one inner layer to describe the ionic dynamics in the nanochannels. Our findings may open the way to unique nanofluidic functionalities, such as energy harvesting/storage and controlling transport at single-molecule and ion levels using the liquid layer near the wall.
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