Understanding the Electrode-Electrolyte Interfaces of Ionic Liquids and Deep Eutectic Solvents

被引:10
|
作者
Coskun, Oguz Kagan [1 ]
Munoz, Miguel [1 ]
Dongare, Saudagar [1 ]
Dean, William [1 ]
Gurkan, Burcu E. [1 ]
机构
[1] Case Western Reserve Univ, Chem & Biomol Engn, Cleveland, OH 44106 USA
关键词
SINGLE-CRYSTAL ELECTRODES; DOUBLE-LAYER CAPACITANCE; ELECTRICAL DOUBLE-LAYER; ALKYL CHAIN-LENGTH; DIFFERENTIAL CAPACITANCE; IMPEDANCE SPECTROSCOPY; CARBON ELECTRODES; GOLD; CO2; ADSORPTION;
D O I
10.1021/acs.langmuir.3c03397
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Developing unconventional electrolytes such as ionic liquids (ILs) and deep eutectic solvents (DESs) has led to remarkable advances in electrochemical energy storage and conversion devices. However, the understanding of the electrode-electrolyte interfaces of these electrolytes, specifically the liquid structure and the charge/electron transfer mechanism and rates, is lacking due to the complexity of molecular interactions, the difficulty in studying the buried interfaces with nanometer-scale resolution, and the distribution of the time scales for the various interfacial events. This Feature Article outlines the standing questions in the field, summarizes some of the exciting approaches and results, and discusses our contributions to probing the electrified interfaces by electrochemical impedance spectroscopy (EIS), surface-enhanced Raman spectroscopy (SERS), and neutron reflectivity (NR). The related findings are analyzed within electrical double-layer models to provide a framework for studying ILs, DESs, and, more broadly, the concentrated hydrogen-bonded electrolytes.
引用
收藏
页码:3283 / 3300
页数:18
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