Mitigating p hosphoric acid migration in high temperature polymer electrolyte membrane fuel cells with hydrophobic polysilsesquioxane-based binders

Cross-linkable organosilsesquioxanes were synthesized for application as catalyst binders in high temperature polymer electrolyte membrane fuel cells (HT-PEMFCs). Four different organic functional groups were examined including methyl, phenyl, fluoroalkyl, and fluorophenyl and their chemical, physic...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2023-08, Vol.11 (34), p.18426-18433
Hauptverfasser: Yoo, Dong-Yeop, Jung, Jiyoon, Park, Young Sang, Choi, Gwan Hyun, Yoon, Ho Gyu, Hwang, Seung Sang, Lee, Albert S.
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Sprache:eng
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Zusammenfassung:Cross-linkable organosilsesquioxanes were synthesized for application as catalyst binders in high temperature polymer electrolyte membrane fuel cells (HT-PEMFCs). Four different organic functional groups were examined including methyl, phenyl, fluoroalkyl, and fluorophenyl and their chemical, physical, surface, and electrochemical properties were characterized. The effect of surface hydrophobicity on a HT-PEMFC membrane electrode assembly was elucidated, showing that organosilsesquioxanes with lower surface tension or higher hydrophobicity towards water and phosphoric acid could be considered as a key parameter for HT-PEMFC performance. Fuel cell tests showed that the pentafluorophenyl-functionalized organosilsesquioxane showed improved H 2 /air performance (a peak power density of 527 mW cm −2 at 0.4 V) compared to the MEA with PTFE (a peak power density of 425 mW cm −2 at 0.4 V). Short term durability tests for 500 h showed that membrane electrode assemblies with alternative binders were stable and the developed organosilsesquioxane binders are a viable alternative to PTFE-based binders, all the while having additional advantages in vastly simplified ink slurry preparation through increased dispersibility in alcohol–water mixtures.
ISSN:2050-7488
2050-7496
DOI:10.1039/D3TA03592A