Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/19275
Full metadata record
DC FieldValueLanguage
dc.contributor.authorWillis-Fox, Niamhpt
dc.contributor.authorMarques, Ana-Teresapt
dc.contributor.authorArlt, Jochenpt
dc.contributor.authorScherf, Ullrichpt
dc.contributor.authorCarlos, Luis D.pt
dc.contributor.authorBurrows, Hugh D.pt
dc.contributor.authorEvans, Rachel C.pt
dc.date.accessioned2017-12-07T19:07:06Z-
dc.date.available2017-12-07T19:07:06Z-
dc.date.issued2015pt
dc.identifier.issn2041-6520pt
dc.identifier.urihttp://hdl.handle.net/10773/19275-
dc.description.abstractPoly(fluorene) conjugated polyelectrolyte (CPE)-di-ureasil organic-inorganic composites have been prepared using a versatile sol-gel processing method, which enables selective localisation of the CPE within the di-ureasil matrix. Introduction of the CPE during the sol-gel reaction leads to a homogeneous distribution of the CPE throughout the di-ureasil, whereas a post-synthesis solvent permeation route leads to the formation of a confined layer of the CPE at the di-ureasil surface. The CPE and the di-ureasil both function as photoactive components, contributing directly to, and enhancing the optical properties of their composite material. The bright blue photoluminescence exhibited by CPE-di-ureasils is reminiscent of the parent CPE; however the distinct contribution of the di-ureasil to the steady-state emission profile is also apparent. This is accompanied by a dramatic increase in the photoluminescence quantum yield to >50%, which is a direct consequence of the synergy between the two components. Picosecond time-correlated single photon counting measurements reveal that the di-ureasil effectively isolates the CPE chains, leading to emissive trap sites which have a high radiative probability. Moreover, intimate mixing of the CPE and the di-ureasil, coupled with their strong spectral overlap, results in efficient excitation energy transfer from the di-ureasil to these emissive traps. Given the simple, solution-based fabrication method and the structural tunability of the two components, this approach presents an efficient route to highly desirable CPE-hybrid materials whose optoelectronic properties may be enhanced and tailored for a targeted application.pt
dc.language.isoengpt
dc.publisherROYAL SOC CHEMISTRYpt
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/262348/EUpt
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/135966/PTpt
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/147332/PTpt
dc.rightsopenAccesspor
dc.subjectLIGHT-EMITTING-DIODESpt
dc.subjectPHOTO-CROSS-LINKINGpt
dc.subjectENERGY-TRANSFERpt
dc.subjectQUANTUM YIELDSpt
dc.subjectORGANIC/INORGANIC HYBRIDSpt
dc.subjectSEMICONDUCTING POLYMERpt
dc.subjectHIGHLY EFFICIENTpt
dc.subjectRECENT PROGRESSpt
dc.subjectSILICA MATRIXpt
dc.subjectSOLAR-CELLSpt
dc.titleSynergistic photoluminescence enhancement in conjugated polymer-di-ureasil organic-inorganic compositespt
dc.typearticlept
dc.peerreviewedyespt
ua.distributioninternationalpt
degois.publication.firstPage7227pt
degois.publication.issue12pt
degois.publication.lastPage7237pt
degois.publication.titleCHEMICAL SCIENCEpt
degois.publication.volume6pt
dc.relation.publisherversion10.1039/c5sc02409apt
dc.identifier.doi10.1039/c5sc02409apt
Appears in Collections:CICECO - Artigos



FacebookTwitterLinkedIn
Formato BibTex MendeleyEndnote Degois 

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