Synergistic photoluminescence enhancement in conjugated polymer-di-ureasil organic-inorganic composites

Detalhes bibliográficos
Autor(a) principal: Willis-Fox, Niamh
Data de Publicação: 2015
Outros Autores: Marques, Ana-Teresa, Arlt, Jochen, Scherf, Ullrich, Carlos, Luis D, Burrows, Hugh D, Evans, Rachel C
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10773/18210
Resumo: Poly(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.
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spelling Synergistic photoluminescence enhancement in conjugated polymer-di-ureasil organic-inorganic compositesPoly(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.Royal Society of Chemistry2017-08-02T14:06:47Z2015-01-01T00:00:00Z2015info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/18210eng2041-653910.1039/c5sc02409aWillis-Fox, NiamhMarques, Ana-TeresaArlt, JochenScherf, UllrichCarlos, Luis DBurrows, Hugh DEvans, Rachel Cinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-02-22T11:33:36Zoai:ria.ua.pt:10773/18210Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T02:52:39.961811Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Synergistic photoluminescence enhancement in conjugated polymer-di-ureasil organic-inorganic composites
title Synergistic photoluminescence enhancement in conjugated polymer-di-ureasil organic-inorganic composites
spellingShingle Synergistic photoluminescence enhancement in conjugated polymer-di-ureasil organic-inorganic composites
Willis-Fox, Niamh
title_short Synergistic photoluminescence enhancement in conjugated polymer-di-ureasil organic-inorganic composites
title_full Synergistic photoluminescence enhancement in conjugated polymer-di-ureasil organic-inorganic composites
title_fullStr Synergistic photoluminescence enhancement in conjugated polymer-di-ureasil organic-inorganic composites
title_full_unstemmed Synergistic photoluminescence enhancement in conjugated polymer-di-ureasil organic-inorganic composites
title_sort Synergistic photoluminescence enhancement in conjugated polymer-di-ureasil organic-inorganic composites
author Willis-Fox, Niamh
author_facet Willis-Fox, Niamh
Marques, Ana-Teresa
Arlt, Jochen
Scherf, Ullrich
Carlos, Luis D
Burrows, Hugh D
Evans, Rachel C
author_role author
author2 Marques, Ana-Teresa
Arlt, Jochen
Scherf, Ullrich
Carlos, Luis D
Burrows, Hugh D
Evans, Rachel C
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Willis-Fox, Niamh
Marques, Ana-Teresa
Arlt, Jochen
Scherf, Ullrich
Carlos, Luis D
Burrows, Hugh D
Evans, Rachel C
description Poly(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.
publishDate 2015
dc.date.none.fl_str_mv 2015-01-01T00:00:00Z
2015
2017-08-02T14:06:47Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10773/18210
url http://hdl.handle.net/10773/18210
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 2041-6539
10.1039/c5sc02409a
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dc.publisher.none.fl_str_mv Royal Society of Chemistry
publisher.none.fl_str_mv Royal Society of Chemistry
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