Please use this identifier to cite or link to this item: https://doi.org/10.1002/marc.201200695
DC FieldValue
dc.titleNear-infrared responsive conjugated polymers to 1.5 μm and beyond: Synthesis and electrochromic switching application
dc.contributor.authorTang, T.
dc.contributor.authorDing, G.
dc.contributor.authorLin, T.
dc.contributor.authorChi, H.
dc.contributor.authorLiu, C.
dc.contributor.authorLu, X.
dc.contributor.authorWang, F.
dc.contributor.authorHe, C.
dc.date.accessioned2014-06-17T07:59:29Z
dc.date.available2014-06-17T07:59:29Z
dc.date.issued2013
dc.identifier.citationTang, T., Ding, G., Lin, T., Chi, H., Liu, C., Lu, X., Wang, F., He, C. (2013). Near-infrared responsive conjugated polymers to 1.5 μm and beyond: Synthesis and electrochromic switching application. Macromolecular Rapid Communications 34 (5) : 431-436. ScholarBank@NUS Repository. https://doi.org/10.1002/marc.201200695
dc.identifier.issn10221336
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/64959
dc.description.abstractAzulene-containing conjugated polymers with near-infrared absorption up to 1.5 μm and beyond are achieved by treating with trifluoroacetic acid (TFA). Density functional theory calculations reveal that the near-infrared absorption arises from a strong intramolecular charge transfer transition on the polymer backbone, and the near-infrared absorption can be tuned by the degree of protonation. Furthermore, TFA treated polymers show a ten-fold enhancement in electrochromic contrast and significantly improved switching stability, suggesting that these polymers are promising candidates for fabrication of the first generation organic near-infrared devices. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/marc.201200695
dc.sourceScopus
dc.subjectazulenes
dc.subjectcharge transfer
dc.subjectconjugated polymers
dc.subjectdensity function theory
dc.subjectnear-infrared absorptions
dc.typeArticle
dc.contributor.departmentMATERIALS SCIENCE AND ENGINEERING
dc.description.doi10.1002/marc.201200695
dc.description.sourcetitleMacromolecular Rapid Communications
dc.description.volume34
dc.description.issue5
dc.description.page431-436
dc.description.codenMRCOE
dc.identifier.isiut000315470400008
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