PEM fuel cell electrocatalyst durability measurements

被引:431
作者
Borup, Rod L.
Davey, John R.
Garzon, Fernando H.
Wood, David L.
Inbody, Michael A.
机构
[1] Los Alamos Natl Lab, Elect & Electrochem Mat & Devices Grp, Los Alamos, NM 87545 USA
[2] Univ New Mexico, Dept Chem & Nucl Engn, Albuquerque, NM USA
关键词
PEM fuel cell durability; platinum electrocatalyst; electrochemically active surface area; catalyst aging; electrochemical potential cycling; fuel cell drive cycle;
D O I
10.1016/j.jpowsour.2006.03.009
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
Electrode material durability is an important factor in limiting the commercialization of polymer electrolyte membrane fuel cells (PEMFCS). PEMFCs typically use carbon supported nanometer sized Pt and/or Pt alloy catalysts for both anode and cathode. Electrocatalyst surface area loss is due to the growth of platinum particles. Particle size growth is accelerated by potential cycling whether due to artificial potential cycling or by cycling during fuel cell operation. Catalysts were analyzed by X-ray diffraction (XRD) to detemtine the degree of electrocatalyst sintering. Cathode Pt particle size growth is a function of temperature, test length and potential. The largest increase in cathode Pt particle size was observed during potential cycling experiments and increased with increasing potential. During single cell durability testing, the cathode catalyst particle size grew from about 1.9 to 3.5 nm during the drive cycle experiments over 1200 h of testing. This extent of growth was greater than that observed during steady-state testing, where the particles grew to 2.6 nm at 900 h and 3.1 nm over 3500 h. During cycling measurements, catalyst coarsening rates exhibited a linear increase with temperature. Low relative humidity decreased platinum particle growth, but substantially increased carbon loss. Carbon corrosion of the electrode catalyst layer was found to increase with increasing potential and decreasing humidity. 0 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:76 / 81
页数:6
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