Electrochemical durability of gas diffusion layer under simulated proton exchange membrane fuel cell conditions
An effective ex-situ method for characterizing electrochemical durability of a gas diffusion layer (GDL) under simulated polymer electrolyte membrane fuel cell (PEMFC) conditions is reported in this article. Electrochemical oxidation of the GDLs are studied following potentiostatic treatments up to...
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Veröffentlicht in: | International journal of hydrogen energy 2009-10, Vol.34 (19), p.8185-8192 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | An effective ex-situ method for characterizing electrochemical durability of a gas diffusion layer (GDL) under simulated polymer electrolyte membrane fuel cell (PEMFC) conditions is reported in this article. Electrochemical oxidation of the GDLs are studied following potentiostatic treatments up to 96
h holding at potentials from 1.0 to 1.4
V (vs.SCE) in 0.5
mol
L
−1 H
2SO
4. From the analysis of morphology, resistance, gas permeability and contact angle, the characteristics of the fresh GDL and the oxidized GDLs are compared. It is found that the maximum power densities of the fuel cells with the oxidized GDLs hold at 1.2 and 1.4
V (vs.SCE) for 96
h decreased 178 and 486
mW
cm
−2, respectively. The electrochemical impedance spectra measured at 1500
mA
cm
−2 are also presented and they reveal that the ohmic resistance, charge-transfer and mass-transfer resistances of the fuel cell changed significantly due to corrosion at high potential. |
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ISSN: | 0360-3199 1879-3487 |
DOI: | 10.1016/j.ijhydene.2009.07.085 |