Degradation behavior of galvanostatic and galvanodynamic cells for hydrogen production from high temperature electrolysis of water

High temperature electrolysis of water using solid oxide electrochemical cells (SOEC) is a promising technology for hydrogen production with high energy efficiency and may promote decarbonization when coupled with renewable energy sources and excess heat from nuclear reactors. Apart from the technoeconomic considerations, commercial deployment of this technology critically depends on the long-term performance and durability of SOEC cells/stacks, especially under dynamic operations to withstand the intermittency of renewable energy. Herein, SOEC operation was conducted under galvanodynamic conditions and compared with galvanostatic cells to examine the effect on degradation behavior at an average current density of −0.75 A cm −2 at 750 °C. While dynamic operation shows no significant impact on the overall degradation rates compared to constant current operation, minor performance improvement was observed at potentials above 1.5 V when switched to galvanodynamic mode. The relatively lower overpotential during dynamic operation could not be explained by the negligible changes in the electrochemical impedance or cell temperature. Multiphysics modeling reveals that the oxygen partial pressure (P O2 ) in the electrolyte oscillates with the alternating current density under dynamic operations. The minor improvement in cell performance under dynamic mode might be associated with the relatively lower P O2 buildup as compared with that under galvanostatic operation. In addition, dynamic operation at high frequencies could effectively lower the extreme P O2 in the electrolyte, thus relieving stresses in the cells and alleviating cell degradation. • P O2 buildup is major cause of SOEC degradation under current driven operation. • Multiscale modeling shows dynamic operation can alleviate P O2 buildup. • Dynamic operation shows stability and minor performance improvement. • Thermal imaging setup confirms consistency in cell temperature. • Modeling results suggest greater benefit at higher frequency/current.

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Publication Details

Journal
International Journal of Hydrogen Energy
Published
2024-08-30
DOI
https://doi.org/10.1016/j.ijhydene.2024.08.019
Citations
7
Primary Topic
Advancements in Solid Oxide Fuel Cells
Type
article
Field-Weighted Citation Impact
0.82

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article

Degradation behavior of galvanostatic and galvanodynamic cells for hydrogen production from high temperature electrolysis of water

Cameron Priest, Joshua Gomez, Micah Casteel, Jeremy Hartvigsen et al.
7 citations
International Journal of Hydrogen Energy
Advancements in Solid Oxide Fuel Cells
0.82
article

Degradation behavior of galvanostatic and galvanodynamic cells for hydrogen production from high temperature electrolysis of water

Cameron Priest, Joshua Gomez, Micah Casteel, Jeremy Hartvigsen, Dong Ding, Nicholas Kane, Lu‐Cun Wang, Qian Zhang, Gang Wu
article en
7 citations

Abstract

High temperature electrolysis of water using solid oxide electrochemical cells (SOEC) is a promising technology for hydrogen production with high energy efficiency and may promote decarbonization when coupled with renewable energy sources and excess heat from nuclear reactors. Apart from the technoeconomic considerations, commercial deployment of this technology critically depends on the long-term performance and durability of SOEC cells/stacks, especially under dynamic operations to withstand the intermittency of renewable energy. Herein, SOEC operation was conducted under galvanodynamic conditions and compared with galvanostatic cells to examine the effect on degradation behavior at an average current density of −0.75 A cm −2 at 750 °C. While dynamic operation shows no significant impact on the overall degradation rates compared to constant current operation, minor performance improvement was observed at potentials above 1.5 V when switched to galvanodynamic mode. The relatively lower overpotential during dynamic operation could not be explained by the negligible changes in the electrochemical impedance or cell temperature. Multiphysics modeling reveals that the oxygen partial pressure (P O2 ) in the electrolyte oscillates with the alternating current density under dynamic operations. The minor improvement in cell performance under dynamic mode might be associated with the relatively lower P O2 buildup as compared with that under galvanostatic operation. In addition, dynamic operation at high frequencies could effectively lower the extreme P O2 in the electrolyte, thus relieving stresses in the cells and alleviating cell degradation. • P O2 buildup is major cause of SOEC degradation under current driven operation. • Multiscale modeling shows dynamic operation can alleviate P O2 buildup. • Dynamic operation shows stability and minor performance improvement. • Thermal imaging setup confirms consistency in cell temperature. • Modeling results suggest greater benefit at higher frequency/current.

International Journal of Hydrogen EnergyVol. 86
Idaho National Laboratory (US), University at Buffalo, State University of New York (US)
U.S. Department of Energy, Office of Energy Efficiency and Renewable Energy, National Renewable Energy Laboratory, Lawrence Berkeley National Laboratory, Idaho National Laboratory, Pacific Northwest National Laboratory
Clean water and sanitation
Openalex Percentile: Top 26%
Advancements in Solid Oxide Fuel Cells
0.82
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