journal article·2012

Recoverable Performance Loss Due to Membrane Chemical Degradation in PEM Fuel Cells

Jingxin Zhang, Brian A. Litteer, Frank D. Coms, Rohit Makharia

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Abstract

Recoverable voltage loss was observed for a PEM fuel cell due to membrane chemical degradation under open circuit voltage (OCV) conditions. The anion analysis of the fuel cell effluent water, collected during both the OCV hold and voltage recovery stages, indicates that sulfate release rate is much higher during recovery than that during the OCV hold. The surge in sulfate anion release occurs simultaneously with the recovery of fuel cell voltage. It was found that the reversible voltage loss, and concurrent sulfate release rate during voltage recovery, is lower for Ce-mitigated NRE211 membrane compared to as-received membrane. The recoverable voltage loss is proposed to be mainly due to the sulfate anion generated by membrane chemical degradation adsorbing onto the platinum catalyst surface.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Fuel Cells and Related Materials · Electrocatalysts for Energy Conversion · Membrane-based Ion Separation Techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (35)

Show source-provided references
1. LaConti A. B. Hamadan M. McDonald R. C. , in Handbook of Fuel Cells: Fundamentals, Technology, Applications, Vielstich W. Lamm A. Gasteiger H. , Editors, p. 656, Wiley, New York (2003).
2. Liu H. Coms F. D. Zhang J. Gasteiger H. A. LaConti A. B. , in Polymer Electrolyte Fuel Cell Durability, Büchi F. N. Schmidt T. J. , Editors, p. 71, Springer, New York (2009).10.1007/978-0-387-85536-3_5 ↗
3. 10.1016/j.jpowsour.2008.03.07810.1016/j.jpowsour.2008.03.078 ↗
4. 10.1149/1.226616310.1149/1.2266163 ↗
5. 10.1016/j.jpowsour.2004.01.02310.1016/j.jpowsour.2004.01.023 ↗
6. 10.1016/j.jpowsour.2006.09.02610.1016/j.jpowsour.2006.09.026 ↗
7. 10.1149/1.278102510.1149/1.2781025 ↗
8. 10.1016/j.electacta.2006.03.00810.1016/j.electacta.2006.03.008 ↗
9. 10.1149/1.276424010.1149/1.2764240 ↗
10. 10.1149/1.221970810.1149/1.2219708 ↗
11. 10.1149/1.278102110.1149/1.2781021 ↗
12. 10.1002/fuce.20040005010.1002/fuce.200400050 ↗
13. 10.1149/1.296492410.1149/1.2964924 ↗
14. 10.1021/j100011a00110.1021/j100011a001 ↗
15. 10.1149/1.183764610.1149/1.1837646 ↗
16. 10.1016/j.jpowsour.2010.04.05210.1016/j.jpowsour.2010.04.052 ↗
17. 10.1149/1.222123710.1149/1.2221237 ↗
18. 10.1021/jp071106k10.1021/jp071106k ↗
19. 10.1021/jp003536f10.1021/jp003536f ↗
20. 10.1016/0022-0728(89)85170-810.1016/0022-0728(89)85170-8 ↗
21. 10.1021/jp960632110.1021/jp9606321 ↗
22. 10.1021/jp037593v10.1021/jp037593v ↗
23. 10.1016/j.jpowsour.2007.12.09110.1016/j.jpowsour.2007.12.091 ↗
24. 10.1016/j.jpowsour.2008.04.00910.1016/j.jpowsour.2008.04.009 ↗
25. 10.1016/j.jpowsour.2008.11.02110.1016/j.jpowsour.2008.11.021 ↗
26. 10.1149/1.358104010.1149/1.3581040 ↗
27. 10.1149/1.291644310.1149/1.2916443 ↗
28. 10.1149/1.298201510.1149/1.2982015 ↗
29. Endoh E. Terazono S. , PCT WO 2005/124911 (2005).
30. Endoh E. Terazono S. , US patent 2007/0104994 (2007).
31. 10.1149/1.298196410.1149/1.2981964 ↗
32. 10.1021/la200694a10.1021/la200694a ↗
33. 10.1149/1.278102010.1149/1.2781020 ↗
34. 10.1149/1.298185910.1149/1.2981859 ↗
35. 10.1149/1.280017110.1149/1.2800171 ↗