A Comprehensive Analysis of the Overpotential Losses in Polymer Electrolyte Fuel Cells

被引:4
|
作者
Fikry, Meriem [1 ]
Garcia-Padilla, Alvaro
Herranz, Juan [1 ]
Khavlyuk, Pavel [2 ]
Eychmueller, Alexander [2 ]
Schmidt, Thomas J. [1 ,3 ]
机构
[1] Paul Scherrer Inst, Electrochem Lab, CH-5232 Villigen, Switzerland
[2] Tech Univ Dresden, Phys Chem, D-01062 Dresden, Germany
[3] Swiss Fed Inst Technol, Inst Mol Phys Sci, CH-8093 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
overpotential; mass transport; Pt-Niaerogel; catalysts; electrochemistry; fuelcell; OXYGEN REDUCTION REACTION; TO-CARBON RATIO; PT-NI AEROGELS; RELATIVE-HUMIDITY; TRANSITION-METALS; OXIDE COVERAGE; SURFACE-AREA; MEMBRANE; TEMPERATURE; PLATINUM;
D O I
10.1021/acscatal.3c04797
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
Polymer electrolyte fuel cells (PEFCs) are expected to play a pivotal role in heavy-duty transportation, but careful benchmarking of the kinetics of the O-2-reduction reaction (ORR) and mass transport properties dictating their performance is needed to render them market-competitive. This assessment generally relies on the extrapolation of the kinetic behavior observed at low current densities to the high currents at which mass transport limitations become significant. However, this kinetic regime is generally assumed to obey a simple Tafel law that does not consider the impact of the relative humidity (RH) on the availability of ORR-active sites. To shed light on the implications of this simplified approach, in this study, we compare the ORR parameters and mass transport losses derived from it with those computed using a more complex kinetic model that incorporates site-availability effects. Our results provide an original insight on the impact of the relative humidity on the ORR-performance of catalysts with different active site distributions and show that the mass transport resistances derived by these two quantification procedures are essentially identical as long as the slope of the kinetic Tafel line is adjusted according to the RH.
引用
收藏
页码:1903 / 1913
页数:11
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