Effect of CeOx Crystallite Size on the Chemical Stability of CeOx Nanoparticles

CeOx is an excellent free radical scavenger to improve polymer electrolyte membrane durability. However, this metal oxide will dissolve during accelerated stress testing (AST), with the resulting cations transporting to the cathode catalyst layer (CCL) leading to performance reduction/degradation of...

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Veröffentlicht in:Journal of the Electrochemical Society 2014-01, Vol.161 (10), p.F1075-F1080
Hauptverfasser: Banham, Dustin, Ye, Siyu, Cheng, Tommy, Knights, Shanna, Stewart, S. Michael, Wilson, Mahlon, Garzon, Fernando
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container_end_page F1080
container_issue 10
container_start_page F1075
container_title Journal of the Electrochemical Society
container_volume 161
creator Banham, Dustin
Ye, Siyu
Cheng, Tommy
Knights, Shanna
Stewart, S. Michael
Wilson, Mahlon
Garzon, Fernando
description CeOx is an excellent free radical scavenger to improve polymer electrolyte membrane durability. However, this metal oxide will dissolve during accelerated stress testing (AST), with the resulting cations transporting to the cathode catalyst layer (CCL) leading to performance reduction/degradation of the PEMFC. Controlling the rate of CeOx dissolution is therefore of great importance, as it may be possible to maintain sufficient Ce cations for free radical scavenging while minimizing the impact of these cations on the CCL. Here the effect of CeOx crystallite size on CeOx dissolution was investigated. Three CeOx additives were prepared having crystallite sizes of 6, 13, or 25 nm. An ex-situ method was used to evaluate the chemical stability of these three CeOx samples, as well as one commercially available CeOx. It was determined that surface area, rather than crystallite size, is the best predictor of chemical stability. In-situ membrane electrode assembly AST cycling was then performed, demonstrating that when low loadings of CeOx (0.006 mg/cm2) are used, the ex-situ method correctly predicts trends in end of life (EOL) performance. Finally, it is shown that increasing the anode RH during AST cycling leads to significantly higher EOL performance losses.
doi_str_mv 10.1149/2.0931410jes
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