Kinetics and Thermodynamics of Hydrogen Oxidation and Oxygen Reduction in Hydrophobic Room-Temperature Ionic Liquids

被引:22
|
作者
Rollins, Julie B. [1 ]
Conboy, John C. [1 ]
机构
[1] Univ Utah, Dept Chem, Salt Lake City, UT 84112 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
attenuated total reflection; current density; electrochemistry; electrolytes; Fourier transform spectra; infrared spectra; ionic conductivity; liquid structure; organic compounds; oxidation; reduction (chemical); thermodynamics; FREQUENCY VIBRATIONAL SPECTROSCOPY; PROTON CONDUCTING MEMBRANE; FUEL-CELL ELECTROLYTES; BRONSTED-ACID; MOLTEN-SALTS; PHYSICOCHEMICAL PROPERTIES; ELECTROCHEMICAL-BEHAVIOR; PLATINUM-ELECTRODES; PHYSICAL-PROPERTIES; IMIDAZOLIUM CATION;
D O I
10.1149/1.3143122
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In this study 1-dodecyl-3-methylimidazolium (C(12)mim) bis(pentafluoroethylsulfonyl)imide (BETI) and 1-dodecylimidazolium (C(12)im) BETI hydrophobic room-temperature ionic liquids (RTILs) were synthesized and used as proton-conducting electrolytes in a nonhumidified feed gas electrochemical cell. The ionic conductivities of C(12)mimBETI and C(12)imBETI were similar and increased linearly with an increase in temperature from 20 to 130 degrees C. However, when used in the electrochemical system the protic water-equilibrated C(12)imBETI had a larger maximum current and power density compared to the aprotic water-equilibrated C(12)mimBETI. The effect of water content on the reaction rates and thermodynamics of these hydrophobic RTILs was also examined. The efficiency of the C(12)mimBETI increased upon removal of water while that of the C(12)imBETI decreased in efficiency when water was removed. The water structure in these RTILs was examined using attenuated total internal reflection Fourier transform IR spectroscopy and depended on the chemical structure of the cation. These studies give further insight into the possible mechanism of proton transport in these RTIL systems.
引用
收藏
页码:B943 / B954
页数:12
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