Cathode Loading Impact on Voltage Cycling Induced PEMFC Degradation: A Voltage Loss Analysis

被引:129
作者
Harzer, Gregor S. [1 ,2 ]
Schwaemmlein, Jan N. [1 ,2 ]
Damjanovic, Ana Marija [3 ]
Ghosh, Sourov [1 ,2 ]
Gasteiger, Hubert A. [1 ,2 ]
机构
[1] Tech Univ Munich, Chair Tech Electrochem, Dept Chem, D-85748 Garching, Germany
[2] Tech Univ Munich, Catalysis Res Ctr, D-85748 Garching, Germany
[3] Univ Zagreb, Fac Chem Engn & Technol, Zagreb 10000, Croatia
关键词
MEMBRANE FUEL-CELLS; CO-STRIPPING VOLTAMMOGRAMS; OXYGEN-TRANSPORT RESISTANCE; ACTIVE SURFACE-AREA; X-RAY-SCATTERING; TO-CARBON RATIO; CATALYST LAYER; POTENTIAL DEPENDENCE; ELECTROCHEMICAL IMPEDANCE; PLATINUM DISSOLUTION;
D O I
10.1149/2.0161806jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
This study focuses on voltage cycling induced degradation of cathodes with different loading (0.4 and 0.1 mg(Pt)/cm(2)) when applying square wave or triangular wave based accelerated stress tests (ASTs) between 0.6 and 1.0 V-RHE. The degradation of the H-2/O-2 and H-2/air performance upon extended voltage cycling (up to 30000 cycles) was analyzed in terms of the voltage loss contributions from ORR kinetics, O-2 mass transport resistances and proton conduction resistances in the cathode. The extent of cathode thinning due to carbon support corrosion was determined by post mortem electrode thickness measurements. Square waves were found to cause a more rapid loss of ECSA and mass activity compared to triangular waves, which was shown to be due to the longer hold periods at high potentials rather than to the rate of the potential transient. The observed increase of the O2 mass transport resistance with voltage cycling was found to mainly depend on the available Pt surface area, while mass transport resistances due to carbon corrosion were found to be insignificant. Finally, it was shown that by lowering the upper potential limit to 0.85 V-RHE, low-loaded catalyst layers can sustain 30000 potential cycles without degradation of the H-2/air performance. (C) The Author(s) 2018. Published by ECS.
引用
收藏
页码:F3118 / F3131
页数:14
相关论文
共 64 条
  • [1] Dynamics of Particle Growth and Electrochemical Surface Area Loss due to Platinum Dissolution
    Ahluwalia, Rajesh K.
    Arisetty, Srikanth
    Peng, Jui-Kun
    Subbaraman, Ram
    Wang, Xiaoping
    Kariuki, Nancy
    Myers, Deborah J.
    Mukundan, Rangachary
    Borup, Rodney
    Polevaya, Olga
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2014, 161 (03) : F291 - F304
  • [2] Catalyst Durability in PEM Fuel Cells with Low Platinum Loading
    Arisetty, S.
    Wang, X.
    Ahluwalia, R. K.
    Mukundan, R.
    Borup, R.
    Davey, J.
    Langlois, D.
    Gambini, F.
    Polevaya, O.
    Blanchet, S.
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2012, 159 (05) : B455 - B646
  • [3] Measurement of Oxygen Transport Resistance in PEM Fuel Cells by Limiting Current Methods
    Baker, Daniel R.
    Caulk, David A.
    Neyerlin, Kenneth C.
    Murphy, Michael W.
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2009, 156 (09) : B991 - B1003
  • [4] Temperature and pressure dependence of O2 reduction at Pt | Nafion® 117 and Pt | BAM® 407 interfaces
    Beattie, PD
    Basura, VI
    Holdcroft, S
    [J]. JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1999, 468 (02): : 180 - 192
  • [5] Borup Rodney L., 2015, ECS Transactions, V69, P1029, DOI 10.1149/06917.1029ecst
  • [6] PEM fuel cell electrocatalyst durability measurements
    Borup, Rod L.
    Davey, John R.
    Garzon, Fernando H.
    Wood, David L.
    Inbody, Michael A.
    [J]. JOURNAL OF POWER SOURCES, 2006, 163 (01) : 76 - 81
  • [7] Carter R., 2007, ECS T, V11, P403, DOI DOI 10.1149/1.2780954
  • [8] Heat and Water Transport in Hydrophobic Diffusion Media of PEM Fuel Cells
    Caulk, David A.
    Baker, Daniel R.
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2010, 157 (08) : B1237 - B1244
  • [9] Dissolution of Noble Metals during Oxygen Evolution in Acidic Media
    Cherevko, Serhiy
    Zeradjanin, Aleksandar R.
    Topalov, Angel A.
    Kulyk, Nadiia
    Katsounaros, Ioannis
    Mayrhofer, Karl J. J.
    [J]. CHEMCATCHEM, 2014, 6 (08) : 2219 - 2223
  • [10] Compton R.G., 1996, ELECT POTENTIALS, V1st