Kinetics of oxygen reduction reaction on nanostructured thin-film platinum alloy catalyst

被引:18
作者
Ahluwalia, R. K. [1 ]
Wang, X. [1 ]
Lajunen, A. [2 ]
Steinbach, A. J. [3 ]
Hendricks, S. M. [3 ]
Kurkowski, M. J. [3 ]
Debe, M. K. [3 ]
机构
[1] Argonne Natl Lab, Argonne, IL 60439 USA
[2] Aalto Univ, Sch Engn, Aalto, Finland
[3] 3M Fuel Cell Components Program, St Paul, MN USA
关键词
Polymer electrolyte fuel cells; Alloy catalysts; Oxygen reduction reaction kinetics; Mass activity; Specific activity; RELATIVE-HUMIDITY; CURRENT-DENSITY; ORR;
D O I
10.1016/j.jpowsour.2012.04.077
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
The kinetics of the oxygen reduction reaction (ORR) on nanostructured thin-film (NSTF) ternary PtCoMn catalyst was investigated in 50 cm(2) proton-exchange membrane single cell fixtures. The investigation covered a wide range of oxygen partial pressures (0.2-0.5 atm), temperatures (30-90 degrees C), relative humidities (25-100%), and Pt loadings (0.05-0.2 mg cm(-2)) in the cathode catalyst. The kinetic data were derived from cell polarization curves measured during Galvanodynamic scans from near open-circuit to a high current density and back to near open-circuit. The kinetic data were correlated with a single Tafel equation and a transfer coefficient that is a function of the relative humidity (RH). The correlation indicates a 0.36 order for the O-2 partial pressure, 39.5 kJ mol(-1) activation energy for the temperature dependence, and an additional 0.9 order for RH dependence. The calculated mass activities and specific activities at 0.9 V Ohmic resistance corrected cell voltage, 1 atm H-2 and O-2 partial pressures, 80 degrees C and 100% RH agree well with the measured values of 0.13-0.25 A mg(pt)(-1) and 1.7-2.0 mA cm(pt)(-2) for the cells with different Pt loading. Published by Elsevier B.V.
引用
收藏
页码:77 / 88
页数:12
相关论文
共 19 条
[1]   Oxygen reduction activity of Pt and Pt-Mn-Co electrocatalysts sputtered on nano-structured thin film support [J].
Bonakdarpour, Arman ;
Stevens, Krystal ;
Vernstrom, George D. ;
Atanasoski, Radoslav ;
Schmoeckel, Alison K. ;
Debe, Mark K. ;
Dahn, Jeff R. .
ELECTROCHIMICA ACTA, 2007, 53 (02) :688-694
[2]  
Debe M.K., 2006, ECS T, V3, P835
[3]  
Debe M.K., 2006, ECS T, V1, P51
[4]  
Debe M.K., 2003, Handbook of Fuel Cells: Fundamentals, Technology and Applications, V3
[5]  
Debe M. K., 2005, FUEL CELL SEM PALM S
[6]   High voltage stability of nanostructured thin film catalysts for PEM fuel cells [J].
Debe, Mark K. ;
Schmoeckel, Alison K. ;
Vernstrorn, George D. ;
Atanasoski, Radoslav .
JOURNAL OF POWER SOURCES, 2006, 161 (02) :1002-1011
[7]   Effect of Electrode Surface Area Distribution on High Current Density Performance of PEM Fuel Cells [J].
Debe, Mark K. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2012, 159 (01) :B54-B67
[8]  
DEBE MK, 2006, FUEL CELL SEM HON HI
[9]  
Gasteiger H.A., 2007, J POWER SOURCES, V154, P162
[10]   Study of the exchange current density for the hydrogen oxidation and evolution reactions [J].
Neyerlin, K. C. ;
Gu, Wenbin ;
Jorne, Jacob ;
Gasteiger, Hubert A. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2007, 154 (07) :B631-B635