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Exploiting Dynamic Opening of Apertures in a Partially Fluorinated MOF for Enhancing H-2 Desorption Temperature and Isotope Separation

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dc.contributor.authorZhang, Linda-
dc.contributor.authorJee, Seohyeon-
dc.contributor.authorPark, Jaewoo-
dc.contributor.authorJung, Minji-
dc.contributor.authorWallacher, Dirk-
dc.contributor.authorFranz, Alexandra-
dc.contributor.authorLee, Wonjoo-
dc.contributor.authorYoon, Minyoung-
dc.contributor.authorChoi, Kyungmin-
dc.contributor.authorHirscher, Michael-
dc.contributor.authorOh, Hyunchul-
dc.date.available2021-02-22T05:36:19Z-
dc.date.issued2019-11-
dc.identifier.issn0002-7863-
dc.identifier.issn1520-5126-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/2694-
dc.description.abstractDeuterium has been recognized as an irreplaceable element in industrial and scientific research. However, hydrogen isotope separation still remains a huge challenge due to the identical physicochemical properties of the isotopes. In this paper, a partially fluorinated metal-organic framework (MOF) with copper, a so-called FMOFCu, was investigated to determine the separation efficiency and capacity of the framework for deuterium extraction from a hydrogen isotope mixture. The unique structure of this porous material consists of a trimodal pore system with large tubular cavities connected through a smaller cavity with bottleneck apertures with a size of 3.6 angstrom plus a third hidden cavity connected by an even smaller aperture of 2.5 angstrom. Depending on the temperature, these two apertures show a gate-opening effect and the cavities get successively accessible for hydrogen with increasing temperature. Thermal desorption spectroscopy (TDS) measurements indicate that the locally flexible MOF can separate D-2 from anisotope mixture efficiently, with a selectivity of 14 at 25 K and 4 at 77 K.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherAMER CHEMICAL SOC-
dc.titleExploiting Dynamic Opening of Apertures in a Partially Fluorinated MOF for Enhancing H-2 Desorption Temperature and Isotope Separation-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/jacs.9b10268-
dc.identifier.scopusid2-s2.0-85076597300-
dc.identifier.wosid000503917800044-
dc.identifier.bibliographicCitationJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.141, no.50, pp 19850 - 19858-
dc.citation.titleJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.citation.volume141-
dc.citation.number50-
dc.citation.startPage19850-
dc.citation.endPage19858-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusMETAL-ORGANIC FRAMEWORKS-
dc.subject.keywordPlusGAS-ADSORPTION-
dc.subject.keywordPlusHYDROGEN-
dc.subject.keywordPlusSITES-
dc.subject.keywordPlusD-2-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/jacs.9b10268-
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