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PEMFC Cathode Contamination Evaluation with Membrane Conductivity Cell, CA, CP, CV, EIS, GC/MS and ISE - Acetonitrile
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Acetonitrile contamination in proton exchange membrane fuel cells (PEMFCs) was studied in situ with chronoamperometry, chronopotentiometry, cyclic voltammetry, electrochemical impedance spectroscopy, gas chromatography/mass spectroscopy, and ex situ with a membrane conductivity cell, ion selective electrode. PEMFCs significantly lost and partially regained performance for all tested electrodes. A significant effect on the membrane proton conductivity was noted in PEMFC but not in conductivity cells. The impact was dependent on the applied potential. Acetonitrile adsorption inhibits the hydrogen oxidation/evolution and the Pt oxidation and PtOx reduction reactions. Several peaks located at 0.17/0.22, 0.40/0.58, 0.65/0.78 V, and 0.9 V vs the hydrogen reference electrode were attributed to the redox of acetonitrile intermediates and products. Clear mechanistic insights were highlighted but a more complete integration of all these results and others obtained with a rotating ring/disc electrode (RRDE) will lead to a more definitive version of the acetonitrile contamination mechanism.
Title: PEMFC Cathode Contamination Evaluation with Membrane Conductivity Cell, CA, CP, CV, EIS, GC/MS and ISE - Acetonitrile
Description:
Acetonitrile contamination in proton exchange membrane fuel cells (PEMFCs) was studied in situ with chronoamperometry, chronopotentiometry, cyclic voltammetry, electrochemical impedance spectroscopy, gas chromatography/mass spectroscopy, and ex situ with a membrane conductivity cell, ion selective electrode.
PEMFCs significantly lost and partially regained performance for all tested electrodes.
A significant effect on the membrane proton conductivity was noted in PEMFC but not in conductivity cells.
The impact was dependent on the applied potential.
Acetonitrile adsorption inhibits the hydrogen oxidation/evolution and the Pt oxidation and PtOx reduction reactions.
Several peaks located at 0.
17/0.
22, 0.
40/0.
58, 0.
65/0.
78 V, and 0.
9 V vs the hydrogen reference electrode were attributed to the redox of acetonitrile intermediates and products.
Clear mechanistic insights were highlighted but a more complete integration of all these results and others obtained with a rotating ring/disc electrode (RRDE) will lead to a more definitive version of the acetonitrile contamination mechanism.
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