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dc.contributor.authorKim, Hee Soo-
dc.contributor.authorLee, Chi Ho-
dc.contributor.authorJang, Jue-Hyuk-
dc.contributor.authorKang, Min Seok-
dc.contributor.authorJin, Haneul-
dc.contributor.authorLee, Kug-Seung-
dc.contributor.authorLee, Sang Uck-
dc.contributor.authorYoo, Sung Jong-
dc.contributor.authorYoo, Won Cheol-
dc.date.accessioned2024-01-19T15:30:48Z-
dc.date.available2024-01-19T15:30:48Z-
dc.date.created2021-10-21-
dc.date.issued2021-02-21-
dc.identifier.issn2050-7488-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/117388-
dc.description.abstractThe development of non Pt-based catalysts (non-PBCs) that show excellent oxygen reduction reaction (ORR) activity for high-performance Zn-air battery (ZAB) and anion exchange membrane fuel cell (AEMFC) is highly necessitated. Here, the unprecedented single-atom ORR activity of Fe, Si, and N co-doped carbon (FeSiNC) supported on 3D interconnected mesoporous carbons (25 and 50 nm) derived from silica templates is reported. Si moieties connected to a carbon surface were involved in the formation of an atomically distributed FeSixN4-x site through substitution of Si at the N position in the Fe-N-4 site, which is the ORR active site of the conventional FeNC. FeSiNC with its larger mesopore (50 nm) exhibits outstanding ORR activity comparable to the most efficient non-Pt-based catalysts and enhanced single-cell performances due to its enhanced mass-transport property. According to theoretical calculations, the ORR activity is originated from not only FeSixN4-x sites located at the basal plane and inter-edge sites, but also C sites adjacent to the Si dopant in both edge and basal regions. Therefore, this study provides a facile strategy toward the rational design of inexpensive and highly active ORR catalysts applicable to single-cell devices.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleSingle-atom oxygen reduction reaction electrocatalysts of Fe, Si, and N co-doped carbon with 3D interconnected mesoporosity-
dc.typeArticle-
dc.identifier.doi10.1039/d0ta11208a-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF MATERIALS CHEMISTRY A, v.9, no.7, pp.4297 - 4309-
dc.citation.titleJOURNAL OF MATERIALS CHEMISTRY A-
dc.citation.volume9-
dc.citation.number7-
dc.citation.startPage4297-
dc.citation.endPage4309-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000621407000048-
dc.identifier.scopusid2-s2.0-85101563236-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryEnergy & Fuels-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEnergy & Fuels-
dc.relation.journalResearchAreaMaterials Science-
dc.type.docTypeArticle-
dc.subject.keywordPlusACTIVE-SITES-
dc.subject.keywordPlusFUEL-CELLS-
dc.subject.keywordPlusFE/N/C CATALYSTS-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusALKALINE-
dc.subject.keywordPlusIRON-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusORR-
dc.subject.keywordPlusSPHERES-
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KIST Article > 2021
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