BROWSE

Related Scientist

nanomat's photo.

nanomat
나노입자연구단
more info

ITEM VIEW & DOWNLOAD

Structural modification of electrode for anion exchange membrane fuel cell by controlling ionomer dispersion

DC Field Value Language
dc.contributor.authorSungjun Kim-
dc.contributor.authorAhn, Chi-Yeong-
dc.contributor.authorKaruppannan, Mohanraju-
dc.contributor.authorYung-Eun Sung-
dc.contributor.authorKwon, Oh Joong-
dc.contributor.authorCho, Yong-Hun-
dc.date.accessioned2022-07-29T07:18:10Z-
dc.date.available2022-07-29T07:18:10Z-
dc.date.created2022-01-03-
dc.date.issued2022-04-
dc.identifier.issn0363-907X-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/11981-
dc.description.abstractAn appropriate electrode microstructure design should be necessary to achieve high-performance anion exchange membrane fuel cells (AEMFCs). In general, the electrodes are fabricated from catalyst slurries which contain self-assembled agglomerates of catalyst particles with ionomer dispersed in a solvent. Therefore, solvent nature greatly affects the microstructure of the electrode, such as the pore structure and the formation of triple-phase boundaries for electrochemical reactions. Here, we investigate the influence of solvent on the microstructure of I2 ionomer-based electrode and its performance using three alcohol-based solvents (ethanol, 2-propanol, and 2-methyl-2-propanol [tBuOH)) with different dielectric constants and similar boiling points. Various physical and electrochemical characterization confirmed that the electrode pore structure changes significantly depending on the type of solvent while the electrochemically active surface area hardly changes. Furthermore, the efect of the three electrodes with different pore structures on AEMFC performance is observed for anode and cathode, respectively. It is demonstrated that the porous electrode with large pores is more advantageous in performance than a dense electrode at both the anode and the cathode for AEMFC. Consequently, the membrane electrode assembly with porous tBuOH-based electrodes exhibits more than 40% higher performance (1.32 W cm(-2)) than dense ethanol-based electrodes (0.94 W cm(-2)).-
dc.language영어-
dc.publisherJohn Wiley & Sons Inc.-
dc.titleStructural modification of electrode for anion exchange membrane fuel cell by controlling ionomer dispersion-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000732984900001-
dc.identifier.scopusid2-s2.0-85121497500-
dc.identifier.rimsid77000-
dc.contributor.affiliatedAuthorSungjun Kim-
dc.contributor.affiliatedAuthorYung-Eun Sung-
dc.identifier.doi10.1002/er.7583-
dc.identifier.bibliographicCitationInternational Journal of Energy Research, v.46, no.5, pp.6471 - 6479-
dc.relation.isPartOfInternational Journal of Energy Research-
dc.citation.titleInternational Journal of Energy Research-
dc.citation.volume46-
dc.citation.number5-
dc.citation.startPage6471-
dc.citation.endPage6479-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEnergy & Fuels-
dc.relation.journalResearchAreaNuclear Science & Technology-
dc.relation.journalWebOfScienceCategoryEnergy & Fuels-
dc.relation.journalWebOfScienceCategoryNuclear Science & Technology-
dc.subject.keywordPlusOXYGEN REDUCTION-
dc.subject.keywordPlusCATALYSTS-
dc.subject.keywordPlusSOLVENT-
dc.subject.keywordAuthoranion exchange membrane fuel cell-
dc.subject.keywordAuthordispersion solvent-
dc.subject.keywordAuthormembrane-electrode assembly-
dc.subject.keywordAuthorpore-structure-
Appears in Collections:
Center for Nanoparticle Research(나노입자 연구단) > 1. Journal Papers (저널논문)
Files in This Item:
There are no files associated with this item.

qrcode

  • facebook

    twitter

  • Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
해당 아이템을 이메일로 공유하기 원하시면 인증을 거치시기 바랍니다.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse