A new insight into the chemical degradation of proton exchange membranes in water electrolyzers
The chemical degradation of the proton exchange membrane (PEM) in a water electrolyzer is a significant issue that can lead to device failure and pose safety risks due to increased gas permeability. Currently, it is generally believed that chemical degradation of PEMs occurs primarily at the cathode...
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Published in | Journal of materials chemistry. A, Materials for energy and sustainability Vol. 12; no. 16; pp. 9563 - 9573 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
23.04.2024
|
Subjects | |
Online Access | Get full text |
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Summary: | The chemical degradation of the proton exchange membrane (PEM) in a water electrolyzer is a significant issue that can lead to device failure and pose safety risks due to increased gas permeability. Currently, it is generally believed that chemical degradation of PEMs occurs primarily at the cathode. However, there is a lack of research on the actual location of degradation and more in-depth investigation into the mechanisms of membrane degradation. By investigating the chemical degradation in different operation modes, as well as the
in situ
electrochemical H
2
O
2
detection, we discovered that both the cathode and anode electrodes can generate H
2
O
2
during operation. Furthermore, membrane degradation can be effectively mitigated by doping CeO
2
in either catalyst layer. Based on the analysis and summary of the observed phenomena in the durability tests, we propose a new model for the membrane degradation process, encompassing H
2
O
2
formation and fluoride emission. A 1-D model was also established for quantitative comprehension of the model. This model considers both cathodic and anodic membrane degradation, which could be beneficial for the design of highly durable PEM water electrolyzers.
A new insight to interpret the PEM degradation process in both electrodes of a PEMWE. |
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Bibliography: | Electronic supplementary information (ESI) available. See DOI https://doi.org/10.1039/d3ta05224a |
ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d3ta05224a |