Long-Term Stability of Nanostructured Thin Film Electrodes at Operating Potentials

被引:9
作者
Ahluwalia, R. K. [1 ]
Peng, J. -K. [1 ]
Wang, X. [1 ]
Cullen, D. A. [2 ]
Steinbach, A. J. [3 ]
机构
[1] Argonne Natl Lab, 9700 S Cass Ave, Argonne, IL 60439 USA
[2] Oak Ridge Natl Lab, Oak Ridge, TN 37831 USA
[3] 3M Fuel Cell Components Program, St Paul, MN 55144 USA
关键词
NSTF ELECTRODES; FUEL-CELLS; CATALYSTS; PERFORMANCE; DEGRADATION; DURABILITY; KINETICS;
D O I
10.1149/2.0881704jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Long-term stability of nanostructured thin film (NSTF) catalysts at operating potentials has been investigated. Compared to high surface area Pt/C catalysts, NSTF electrodes show 20-50x smaller F- emission rates (FER) because of their high specific activity for oxygen reduction reaction (ORR), but are susceptible to poisoning by the products of membrane degradation because of their low electrochemically active surface area (ECSA). The observed voltage degradation rates at potentials corresponding to 1-1.5 A/cm(2) current density are much higher than the allowable 13-14 mu V/h. Although F- is not itself responsible for performance decay, cumulative fluoride release (CFR) is a good marker for catalyst surface contamination. The observed performance decay is not only due to loss of active Pt sites but also adsorbed impurities impeding ORR kinetics. There is a strong correlation between measured CFR and observed decrease in specific ORR activity and limiting current density and increase in mass transfer overpotentials. The correlations indicate that the target of < 10% lifetime performance degradation can be achieved by restricting CFR in NSTF electrodes to 0.7 mu g/cm(2), as may be possible with more stable membranes, higher surface area NSTF catalysts, and cell operation at lower temperatures and higher relative humidities. (C) The Author(s) 2017. Published by ECS.
引用
收藏
页码:F306 / F320
页数:15
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