The effect of platinum on carbon corrosion behavior in polymer electrolyte fuel cells

被引:129
作者
Linse, Nicolas [1 ]
Gubler, Lorenz [1 ]
Scherer, Guenther G. [1 ]
Wokaun, Alexander [1 ]
机构
[1] Paul Scherrer Inst, Electrochem Lab, CH-5232 Villigen, Switzerland
关键词
Carbon corrosion; Polymer electrolyte fuel cell; Platinum; Start/stop induced degradation; Catalyst support degradation; OXIDE-FILM FORMATION; START-UP; INDUCED DEGRADATION; SUPPORTED PLATINUM; PEMFC ELECTRODES; REST POTENTIALS; TEMPERATURE; DISSOLUTION; STABILITY; MECHANISM;
D O I
10.1016/j.electacta.2011.06.093
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
To assess the catalytic effect of platinum on the corrosion of the high surface area carbon support, single triangular potential sweeps with various upper and lower limits were applied to fuel cells comprising electrodes having different Pt/C compositions. Carbon loss rates in H-2/N-2 and air/air mode were determined by integration of the resulting CO2 concentration peaks in the exhaust gas of the positive electrode. Generally, the contribution of platinum catalyzed carbon corrosion to total CO2 evolution was found to decrease with increasing upper potential limit. Similar carbon loss rates obtained for Pt/C and pure carbon electrodes in case of lower potential limits of 1.0 V indicate that the catalytic activity of platinum is substantially lowered by the formation of a passivating oxide layer on the platinum particles. Changes in corrosion behavior in the potential range below 0.6 V. which cannot be attributed to platinum effects, are suggested to originate from modifications in carbon surface oxide composition. Due to the high oxygen equilibrium potential of approximately 1 V, carbon corrosion in air/air mode is significantly influenced by platinum oxide formation. However, the polarization of the negative electrode and the influence of platinum oxidation on the equilibrium potential results in a passivating effect that is less pronounced than expected from measurements in H-2/N-2 mode. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7541 / 7549
页数:9
相关论文
共 45 条
[1]   Comprehensive study of the growth of thin oxide layers on Pt electrodes under well-defined temperature, potential, and time conditions [J].
Alsabet, M ;
Grden, M ;
Jerkiewicz, G .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2006, 589 (01) :120-127
[2]  
APPLEBY AJ, 1972, J ELECTROANAL CHEM, V35, P193, DOI 10.1016/S0022-0728(72)80307-3
[3]   An investigation into factors affecting the stability of carbons and carbon supported platinum and platinum/cobalt alloy catalysts during 1.2 V potentiostatic hold regimes at a range of temperatures [J].
Ball, S. C. ;
Hudson, S. L. ;
Thompsett, D. ;
Theobald, B. .
JOURNAL OF POWER SOURCES, 2007, 171 (01) :18-25
[4]   The effect of humidity and oxygen partial pressure on degradation of Pt/C catalyst in PEM fuel cell [J].
Bi, Wu ;
Sun, Qunhui ;
Deng, Win ;
Fuller, Thomas F. .
ELECTROCHIMICA ACTA, 2009, 54 (06) :1826-1833
[5]   PEM fuel cell electrocatalyst durability measurements [J].
Borup, Rod L. ;
Davey, John R. ;
Garzon, Fernando H. ;
Wood, David L. ;
Inbody, Michael A. .
JOURNAL OF POWER SOURCES, 2006, 163 (01) :76-81
[6]   Study of electrochemical instabilities of PEMFC electrodes in aqueous solution by means of membrane inlet mass spectrometry [J].
Chaparro, A. M. ;
Mueller, N. ;
Atienza, C. ;
Daza, L. .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2006, 591 (01) :69-73
[7]   Model study on the stability of carbon support materials under polymer electrolyte fuel cell cathode operation conditions [J].
Colmenares, L. C. ;
Wurth, A. ;
Jusys, Z. ;
Behm, R. J. .
JOURNAL OF POWER SOURCES, 2009, 190 (01) :14-24
[8]   ELECTROCHEMICAL OXIDE FILM FORMATION AT NOBLE-METALS AS A SURFACE-CHEMICAL PROCESS [J].
CONWAY, BE .
PROGRESS IN SURFACE SCIENCE, 1995, 49 (04) :331-452
[9]  
Dam VAT, 2007, J ELECTROCHEM SOC, V154, pB494, DOI 10.1149/1.2714327
[10]  
Dross R., 2007, ECS T, V11, P1059