Transient and Steady State Two-Phase Flow in Anodic Porous Transport Layer of Proton Exchange Membrane Water Electrolyzer
Source abstract
Abstract
Mass transport losses are one of the least understood contributors to the over potential in proton exchange membrane water electrolyzers. In order to explore the possible contribution of porous media two phase flow to these losses, we have used neutron-imaging techniques and took a closer look at water and gas distribution profiles at various current densities, ranging from kinetic to mass transport-governed regions at ambient and elevated pressures. Gas volume and velocity have been computed through quantified neutron images and the two-phase flow regime has been identified. Using sub-second imaging, information on dynamics of gas pathway establishment and re-imbibition during startup and shutdown of electrolyzers has been acquired. Using X-ray tomography and simulated mercury intrusion porosimetry coupled with capillary pressure calculations, the hydrophilicity of the internal surfaces of the porous transport layer material has been determined.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Hybrid Renewable Energy Systems · Hydrogen Storage and Materials · Fuel Cells and Related Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (42)
Show source-provided references
1. International Energy Agency IEA · World Energy Outlook · 2017 · 2017 · 24
2. 10.1016/j.ijhydene.2013.01.15110.1016/j.ijhydene.2013.01.151 ↗
3. Babic U. · J. Electrochem. Soc. · 2017 · 164 · F38710.1149/2.1441704jes ↗
4. Weiß A. · J. Electrochem. Soc. · 2019 · 166 · F48710.1149/2.0421908jes ↗
5. 10.1016/j.jpowsour.2016.01.10010.1016/j.jpowsour.2016.01.100 ↗
6. 10.1515/green-2013-000110.1515/green-2013-0001 ↗
7. 10.1016/j.apenergy.2016.01.03810.1016/j.apenergy.2016.01.038 ↗
8. 10.1016/j.renene.2015.07.06610.1016/j.renene.2015.07.066 ↗
9. 10.1016/j.rser.2017.09.00310.1016/j.rser.2017.09.003 ↗
10. 10.2533/chimia.2015.60310.2533/chimia.2015.603 ↗
11. 10.1021/acs.chemmater.6b0262510.1021/acs.chemmater.6b02625 ↗
12. Bernt M. · J. Electrochem. Soc. · 2018 · 165 · F30510.1149/2.0641805jes ↗
13. 10.1021/acs.chemmater.7b0076610.1021/acs.chemmater.7b00766 ↗
14. 10.1039/C5NJ02400E10.1039/C5NJ02400E ↗
15. 10.1039/C5SC00518C10.1039/C5SC00518C ↗
16. 10.1016/j.ijhydene.2014.02.08210.1016/j.ijhydene.2014.02.082 ↗
17. 10.1039/C9EE01018A10.1039/C9EE01018A ↗
18. Suermann M. · J. Electrochem. Soc. · 2017 · 164 · F97310.1149/2.13517109jes ↗
19. Schuler T. · J. Electrochem. Soc. · 2019 · 166 · F27010.1149/2.0561904jes ↗
20. Schuler T. · J. Electrochem. Soc. · 2019 · 166 · F55510.1149/2.1241908jes ↗
21. Greszler T. A. · J. Electrochem. Soc. · 2012 · 159 · F83110.1149/2.061212jes ↗
22. 10.1016/j.ijhydene.2016.09.11410.1016/j.ijhydene.2016.09.114 ↗
23. 10.1016/j.jpowsour.2019.22731210.1016/j.jpowsour.2019.227312 ↗
24. 10.1016/j.elecom.2015.03.00910.1016/j.elecom.2015.03.009 ↗
25. Selamet O. F. · ECS Trans. · 2011 · 41 · 34910.1149/1.3635568 ↗
26. 10.1016/j.jpowsour.2018.04.04410.1016/j.jpowsour.2018.04.044 ↗
27. Immerz C. · J. Electrochem. Soc. · 2018 · 16510.1149/2.0411816jes ↗
28. Arbabi F. · J. Electrochem. Soc. · 2016 · 163 · F306210.1149/2.0091611jes ↗
29. 10.1016/j.electacta.2018.04.14410.1016/j.electacta.2018.04.144 ↗
30. Seweryn J. · J. Electrochem. Soc. · 2016 · 163 · F300910.1149/2.0641607jes ↗
31. 10.1016/j.jpowsour.2014.02.04210.1016/j.jpowsour.2014.02.042 ↗
32. 10.1563/1548-1336(1999)025<0230:CAMODI>2.3.CO;210.1563/1548-1336(1999)025<0230:CAMODI>2.3.CO;2 ↗
33. 10.1364/OE.26.01576910.1364/OE.26.015769 ↗
34. 10.1016/j.elecom.2008.06.01610.1016/j.elecom.2008.06.016 ↗
35. 10.1080/1058975010895307510.1080/10589750108953075 ↗
36. 10.1016/j.nima.2005.01.32110.1016/j.nima.2005.01.321 ↗
37. Schuler T. · J. Electrochem. Soc. · 2019 · 166
38. 10.1017/S002211208800095310.1017/S0022112088000953 ↗
39. 10.1021/ef101732k10.1021/ef101732k ↗
40. 10.1016/j.ijhydene.2010.01.05010.1016/j.ijhydene.2010.01.050 ↗
41. Forner-Cuenca A. · J. Electrochem. Soc. · 2016 · 163 · F103810.1149/2.0511609jes ↗
42. 10.1016/j.protcy.2016.01.09410.1016/j.protcy.2016.01.094 ↗