Effect of Temperature and Pressure on the Kinetics of the Oxygen Reduction Reaction

被引:39
|
作者
Tse, Edmund C. M. [1 ]
Gewirth, Andrew A. [1 ,2 ]
机构
[1] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[2] Kyushu Univ, Int Inst Carbon Neutral Energy Res WPI I2CNER, Fukuoka 8128581, Japan
来源
JOURNAL OF PHYSICAL CHEMISTRY A | 2015年 / 119卷 / 08期
关键词
PEM FUEL-CELL; LASER-INDUCED FLUORESCENCE; BATTERY ELECTRIC VEHICLES; RING-DISK ELECTRODE; IN-SITU FTIR; SUPERCRITICAL FLUIDS; POLYCRYSTALLINE PLATINUM; HYDROGEN ADSORPTION; HYDROXYL RADICALS; SINGLE-CRYSTALS;
D O I
10.1021/acs.jpca.5b00572
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Fundamental understanding of the oxygen reduction reaction in aqueous medium at temperatures above 100 °C is lacking due to the practical limitations related to the harsh experimental conditions. In this work, the challenge to suppress water from boiling was overcome by conducting the electrochemical investigation under pressurized conditions. A striking improvement in the kinetics of the electrocatalytic reduction of O2 by about 150 fold relative to room temperature and pressure was recorded under an O2 pressure of 3.4 MPa at 200°C in basic aqueous environment. To deconvolute the combined effect of temperature and pressure, the underlying variables that dictate the observed O2 reduction kinetics of Pt and carbon electrodes were examined individually. O2 availability at the electrode-solution interface was controlled by the interplay between the diffusion coefficient and concentration of O2. Accurate knowledge of the temperature and pressure dependence of O2 availability at the electrode surface, the Tafel slope, the transfer coefficient, and the electrochemical active surface area was required to correctly account for the enhanced O2 reduction kinetics. © 2015 American Chemical Society.
引用
收藏
页码:1246 / 1255
页数:10
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