Experimental Evidence of Long-Lived Electric Fields of Ionic Liquid Bilayers

被引:40
作者
Belotti, Mattia [1 ]
Lyu, Xin [1 ]
Xu, Longkun [2 ]
Halat, Peter [3 ]
Darwish, Nadim [1 ]
Silvester, Debbie S. [1 ]
Goh, Ching [1 ]
Izgorodina, Ekaterina I. [3 ]
Coote, Michelle L. [2 ]
Ciampi, Simone [1 ]
机构
[1] Curtin Univ, Sch Mol & Life Sci, Bentley, WA 6102, Australia
[2] Australian Natl Univ, ARC Ctr Excellence Electromat Sci, Res Sch Chem, Canberra, ACT 2601, Australia
[3] Monash Univ, Sch Chem, Clayton, Vic 3800, Australia
基金
澳大利亚研究理事会;
关键词
FREQUENCY GENERATION SPECTROSCOPY; DOUBLE-LAYER; DIFFERENTIAL CAPACITANCE; ELECTROSTATIC CATALYSIS; FREE ANALYZER; INTERFACE; ELECTROLYTE; COEFFICIENTS; RELAXATION; MONOLAYERS;
D O I
10.1021/jacs.1c06385
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein we demonstrate that ionic liquids can form long-lived double layers, generating electric fields detectable by straightforward open circuit potential (OCP) measurements. In imidazolium-based ionic liquids an external negative voltage pulse leads to an exceedingly stable near-surface dipolar layer, whose field manifests as long-lived (similar to 1-100 h) discrete plateaus in OCP versus time traces. These plateaus occur within an ionic liquid-specific and sharp potential window, defining a simple experimental method to probe the onset of interfacial ordering phenomena, such as overscreening and crowding. Molecular dynamics modeling reveals that the OCP arises from the alignment of the individual ion dipoles to the external electric field pulse, with the magnitude of the resulting OCP correlating with the product of the projected dipole moment of the cation and the ratio between the cation diffusion coefficient and its volume. Our findings also reveal that a stable overscreened structure is more likely to form if the interface is first forced through crowding, possibly accounting for the scattered literature data on relaxation kinetics of near-surface structures in ionic liquids.
引用
收藏
页码:17431 / 17440
页数:10
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