离子液体
材料科学
离子电导率
纳米尺度
电导率
离子键合
薄膜
基质(水族馆)
纳米-
化学物理
分子动力学
纳米技术
化学工程
复合材料
离子
电解质
物理化学
化学
计算化学
有机化学
电极
工程类
催化作用
地质学
海洋学
作者
Shingo Maruyama,Ida Bagus Hendra Prastiawan,Kaho Toyabe,Yuji Higuchi,Tomoyuki Koganezawa,Momoji Kubo,Yuji Matsumoto
出处
期刊:ACS Nano
[American Chemical Society]
日期:2018-09-10
卷期号:12 (10): 10509-10517
被引量:38
标识
DOI:10.1021/acsnano.8b06386
摘要
Thin film approaches are powerful methods for gaining a nanoscale understanding of interfacial ionic liquids (ILs) in the vicinity of solids. These approaches are used to directly elucidate the interfacial contributions to the physical properties of ILs as nanoscale thin films have significant proportions of the surface or interface region with respect to their total volume. Here, we report the growth of a uniform [emim][TFSA] thin film ionic liquid on a chemically modified, well-wettable sapphire, thereby allowing the in situ measurement of its ionic conductivity on the nanoscale. We observed the thickness-dependent behavior of the ionic conductivity, which gradually decreased especially when the thickness was less than 10 nm, and found it to be quantitatively analyzed well by using an empirical two-layer model. The molecular dynamics (MD) simulations show that the thickness-dependent ionic conductivity originates from the solid-like structuring of the IL near the substrate, reproducing a thickness-dependent ionic conductivity. The MD simulation results suggest that the thickness of the low conductivity region determined in the two-layer model should roughly correspond to the thickness of the solid-like structuring of the IL near the substrate.
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