铂金
交换电流密度
化学
阳极
电解质
氢
动力学
旋转圆盘电极
质子交换膜燃料电池
无机化学
分析化学(期刊)
碱性燃料电池
标准氢电极
电化学
催化作用
电极
循环伏安法
物理化学
参比电极
膜
物理
有机化学
量子力学
生物化学
色谱法
塔菲尔方程
作者
Wenchao Sheng,Hubert A. Gasteiger,Yang Shao‐Horn
出处
期刊:Journal of The Electrochemical Society
[The Electrochemical Society]
日期:2010-01-01
卷期号:157 (11): B1529-B1529
被引量:1541
摘要
The kinetics of the hydrogen oxidation reaction (HOR) and hydrogen evolution reaction (HER) on polycrystalline platinum [Pt(pc)] and high surface area carbon-supported platinum nanoparticles (Pt/C) were studied in 0.1 M KOH using rotating disk electrode (RDE) measurements. After corrections of noncompensated solution resistance from ac impedance spectroscopy and of hydrogen mass transport in the HOR branch, the kinetic current densities were fitted to the Butler–Volmer equation using a transfer coefficient of , from which HOR/HER exchange current densities on Pt(pc) and Pt/C were obtained, and the HOR/HER mechanisms in alkaline solution were discussed. Unlike the HOR/HER rates on Pt electrodes in alkaline solution, the HOR/HER rates on a Pt electrode in 0.1 M were limited entirely by hydrogen diffusion, which renders the quantification of the HOR/HER kinetics impossible by conventional RDE measurements. The simulation of the hydrogen anode performance based on the specific exchange current densities of the HOR/HER at illustrates that in addition to the oxygen reduction reaction cell voltage loss on the cathode, the slow HOR kinetics are projected to cause significant anode potential losses in alkaline fuel cells for low platinum loadings ( at and ), contrary to what is reported for proton exchange membrane fuel cells.
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