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Enhanced chemical durability of polymer electrolyte membrane fuel cells by crown ether grafted carbon nanotube

Low chemical stability of membrane-electrode assembly (MEA) remains a major obstacle to commercialization of polymer electrolyte membrane fuel cells (PEMFCs) for fuel cell electric vehicles (FCEVs). In this study, we doubly anchored cerium-ion in the catalyst layer by forming a complex with the 15-c...

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Published in:Journal of alloys and compounds 2022-12, Vol.928, p.167227, Article 167227
Main Authors: Oh, Keun-Hwan, Goo, Youngmo, Kim, Myounghwan, Park, Jiyoung, Nam, Kwan Woo, Kim, Heejin
Format: Article
Language:English
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Summary:Low chemical stability of membrane-electrode assembly (MEA) remains a major obstacle to commercialization of polymer electrolyte membrane fuel cells (PEMFCs) for fuel cell electric vehicles (FCEVs). In this study, we doubly anchored cerium-ion in the catalyst layer by forming a complex with the 15-crown-5-ether and additionally grafting to the multiwall carbon nanotube (Ce/CRE-graft-CNT) as a long-lasting radical scavenger. To confirm the effect of Ce/CRE-graft-CNT on chemical durability, the binding energy between the cerium-ion and crown ether was identified with DFT calculations. The incorporation of Ce/CRE-graft-CNT into catalyst layer decreases decay rate of open circuit voltage (OCV) by 4 times from 2.13 to 0.56 mV h−1 for 210 h operation. The performance retention of the Ce/CRE-graft-CNT (70.8 %) at 0.6 V is also higher than that of the Ce/CRE-blend-CNT (44.8 %). The results indicate that the doubly anchored Ce/CRE-graft-CNT has a more retention capability as a radical scavenger. Therefore, a tightly bounded cerium-ion/crown ether complex with CNT can provide a strategy to improve the chemical durability of MEAs. •The cerium-ion/crown ether complex is grafted to the multiwall carbon nanotube.•The binding energy among the Ce, CRE, and CNT is calculated from DFT method.•The chemical durability is improved by the Ce/CRE-graft-CNTs as a radical scavenger.
ISSN:0925-8388
1873-4669
DOI:10.1016/j.jallcom.2022.167227