In Situ Probing of Ion Ordering at an Electrified Ionic Liquid/Au Interface

被引:15
|
作者
Sitaputra, Wattaka [1 ]
Stacchiola, Dario [1 ]
Wishart, James F. [2 ]
Wang, Feng [3 ]
Sadowski, Jerzy T. [1 ]
机构
[1] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
[2] Brookhaven Natl Lab, Chem Div, Upton, NY 11973 USA
[3] Brookhaven Natl Lab, Sustainable Energy Technol Dept, Upton, NY 11973 USA
关键词
electric double layers; ionic liquids; photoemission electron microscopy; DOUBLE-LAYER; SURFACE; METALLIZATION; ELECTROLYTES; SPECTROSCOPY; ADSORPTION; DEPOSITION; MOBILITY; AU(111); FILMS;
D O I
10.1002/adma.201606357
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Charge transport at the interface of electrodes and ionic liquids is critical for the use of the latter as electrolytes. A room-temperature ionic liquid, 1-ethyl-2,3-dimethylimidazolium bis(trifluoromethanesulfonyl)imide (EMMIM TFSI), is investigated in situ under applied bias voltage with a novel method using low-energy electron and photoemission electron microscopy. Changes in photoelectron yield as a function of bias applied to electrodes provide a direct measure of the dynamics of ion reconfiguration and electrostatic responses of the EMMIM TFSI. Long-range and correlated ionic reconfigurations that occur near the electrodes are found to be a function of temperature and thickness, which, in turn, relate to ionic mobility and different configurations for out-of-plane ordering near the electrode interfaces, with a critical transition in ion mobility for films thicker than three monolayers.
引用
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页数:7
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