journal article·2021-04-26Open access

Compressive Creep of Polymer Electrolyte Membranes: A Case Study for Electrolyzers

Claire Arthurs, Ahmet Kusoglu

ACS Applied Energy Materials· Volume 4· Issue 4

Abstract

For proton-exchange membrane (PEM) water electrolyzers to be commercially feasible, PEMs must perform over long lifetimes in liquid environments under compression while maintaining mechanical stability. A hydrated environment, while inherent for operation and conductivity, undermines PEM stability. Mechanical stability of PEMs is commonly characterized in tension, which is not applicable to electrolyzers, wherein PEMs could undergo high pressures. In this study, a compression creep procedure is developed using a custom-designed setup to monitor creep response of hydrated PEMs. Our results show that PEMs exhibit continuous creep response under compression over 24 h, with a dependence on the applied pressure and hydration state.
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Research context

OpenAlex topics: Fuel Cells and Related Materials · Hybrid Renewable Energy Systems · Advanced battery technologies research

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Affiliations

Energy Conversion Group, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States

Department of Mechanical Engineering, University of California Berkeley, Berkeley, California 94720, United States

Funding

Fuel Cell Technologies Office

References (30)

Show source-provided references
1. 10.1016/j.cattod.2015.10.01910.1016/j.cattod.2015.10.019 ↗
2. 10.1149/1.348449610.1149/1.3484496 ↗
3. 10.1149/07514.0395ecst10.1149/07514.0395ecst ↗
4. 10.1016/j.ijhydene.2013.01.15110.1016/j.ijhydene.2013.01.151 ↗
5. 10.1149/2.1441704jes10.1149/2.1441704jes ↗
6. 10.1149/2.1451910jes10.1149/2.1451910jes ↗
7. Department of Energy. Department of Energy Hydrogen Program Plan, 2020; pp 1–51.
8. Cropley C. C. · 200810.2172/926321 ↗
9. 10.1007/s10800-012-0490-510.1007/s10800-012-0490-5 ↗
10. 10.1023/a:100347730533610.1023/a:1003477305336 ↗
11. 10.1021/acs.chemrev.6b0015910.1021/acs.chemrev.6b00159 ↗
12. 10.1016/j.memsci.2012.07.02710.1016/j.memsci.2012.07.027 ↗
13. 10.1021/ma301419s10.1021/ma301419s ↗
14. 10.1016/j.jpowsour.2009.08.01010.1016/j.jpowsour.2009.08.010 ↗
15. 10.1002/polb.2160810.1002/polb.21608 ↗
16. 10.1016/j.msea.2006.03.05510.1016/j.msea.2006.03.055 ↗
17. 10.1590/s0104-1428200200020000810.1590/s0104-14282002000200008 ↗
18. 10.1115/1.297106910.1115/1.2971069 ↗
19. 10.1016/j.jpowsour.2010.03.04710.1016/j.jpowsour.2010.03.047 ↗
20. 10.1016/j.jpowsour.2007.09.09310.1016/j.jpowsour.2007.09.093 ↗
21. 10.1002/pen.2047810.1002/pen.20478 ↗
22. 10.1021/ma802106g10.1021/ma802106g ↗
23. 10.1021/ma200865p10.1021/ma200865p ↗
24. 10.1016/j.polymer.2015.02.04610.1016/j.polymer.2015.02.046 ↗
25. 10.1016/s1007-0214(10)70077-810.1016/s1007-0214(10)70077-8 ↗
26. 10.1149/2.097112jes10.1149/2.097112jes ↗
27. 10.1021/ma801811m10.1021/ma801811m ↗
28. 10.1088/2053-1591/ab008b10.1088/2053-1591/ab008b ↗
29. 10.1002/polb.2085710.1002/polb.20857 ↗
30. 10.1021/acs.macromol.6b0162510.1021/acs.macromol.6b01625 ↗