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dc.creatorOtal, E.H.es
dc.creatorKim, M.L.es
dc.creatorCalvo Roggiani, Mauricioes
dc.creatorKarvonen, L.es
dc.creatorFabregas, I.O.es
dc.creatorSierra, C.A.es
dc.creatorHinestroza, J.P.es
dc.date.accessioned2018-11-20T18:04:03Z
dc.date.available2018-11-20T18:04:03Z
dc.date.issued2016
dc.identifier.citationOtal, E.H., Kim, M.L., Calvo Roggiani, M., Karvonen, L., Fabregas, I.O., Sierra, C.A. y Hinestroza, J.P. (2016). A panchromatic modification of the light absorption spectra of metal–organic frameworks. Chemical Communications, 52, 6665-6668.
dc.identifier.issn1359-7345es
dc.identifier.issn1364-548Xes
dc.identifier.urihttps://hdl.handle.net/11441/80406
dc.description.abstractThe optical absorption of UiO-66–NH2 MOF was red-shifted using a diazo-coupling reaction. The modifications performed with naphthols and aniline yielded reddish samples, and the modifications with diphenylaniline yielded dark violet ones. The photocatalytic activity of these modified MOFs was assessed for methylene blue degradation, showing a good performance relative to traditional TiO2. The degradation performance was found to correlate with the red shift of the absorption edge. These findings suggest potential applications of these materials in photocatalysis and in dye sensitized solar cells.es
dc.formatapplication/pdfes
dc.language.isoenges
dc.publisherRoyal Society of Chemistry (Great Britain)es
dc.relation.ispartofChemical Communications, 52, 6665-6668.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleA panchromatic modification of the light absorption spectra of metal–organic frameworkses
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/acceptedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.relation.publisherversionhttp://dx.doi.org/10.1039/C6CC02319Ces
dc.identifier.doi10.1039/C6CC02319Ces
idus.format.extent4 p.es
dc.journaltitleChemical Communicationses
dc.publication.volumen52es
dc.publication.initialPage6665es
dc.publication.endPage6668es

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