TY - JOUR
T1 - Hydrogen oxidation and evolution reaction kinetics on platinum
T2 - Acid vs alkaline electrolytes
AU - Sheng, Wenchao
AU - Gasteiger, Hubert A.
AU - Shao-Horn, Yang
PY - 2010
Y1 - 2010
N2 - 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 α=0.5, 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 HClO4 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 80°C 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 (<130 mV at 0.05 mgPt/cmanode2and 1.5 A/cmanode2), contrary to what is reported for proton exchange membrane fuel cells.
AB - 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 α=0.5, 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 HClO4 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 80°C 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 (<130 mV at 0.05 mgPt/cmanode2and 1.5 A/cmanode2), contrary to what is reported for proton exchange membrane fuel cells.
UR - http://www.scopus.com/inward/record.url?scp=77957692480&partnerID=8YFLogxK
U2 - 10.1149/1.3483106
DO - 10.1149/1.3483106
M3 - Article
AN - SCOPUS:77957692480
SN - 0013-4651
VL - 157
SP - B1529-B1536
JO - Journal of the Electrochemical Society
JF - Journal of the Electrochemical Society
IS - 11
ER -