Targeted design leads to tunable photoluminescence from perylene dicarboxdiimide–poly(oxyalkylene)/siloxane hybrids for luminescent solar concentrators. Issue 18 (31st March 2016)
- Record Type:
- Journal Article
- Title:
- Targeted design leads to tunable photoluminescence from perylene dicarboxdiimide–poly(oxyalkylene)/siloxane hybrids for luminescent solar concentrators. Issue 18 (31st March 2016)
- Main Title:
- Targeted design leads to tunable photoluminescence from perylene dicarboxdiimide–poly(oxyalkylene)/siloxane hybrids for luminescent solar concentrators
- Authors:
- Meazzini, Ilaria
Willis-Fox, Niamh
Blayo, Camille
Arlt, Jochen
Clément, Sébastien
Evans, Rachel C. - Abstract:
- Abstract : The chain length and branching of the organic backbone of poly(oxyalkylene)/siloxane ureasils can be used to control the placement and orientation of a covalently-grafted perylene, leading to tunable photoluminescence. Abstract : A series of organic–inorganic hybrid materials in which a perylene carboxdiimide-bridged triethoxysilane (PDI-Sil ) is covalently grafted to the siliceous domains of poly(oxyalkylene)/siloxane hybrids from the ureasil family has been synthesised (PDI-Sil -ureasils), with the aim of tailoring the optical properties towards their future application in luminescent solar concentrators (LSCs). Steady-state and time-resolved photoluminescence studies revealed that the ureasil host is able to isolatePDI-Sil, which inhibits the formation of aggregates. The ureasil also functions as an active host, with its intrinsic photoluminescence contributing to the optical properties of the hybrid material. Through strategic variation of the branching and molecular weight of the poly(oxyalkylene) backbone, it was shown that the efficiency of energy transfer from the ureasil host to thePDI-Sil can be modulated, which tunes the emission colour from pink to orange. The chain length, rather than the number of branches, on the poly(oxyalkylene) backbone was shown to influence the photoluminescence most significantly. Since ureasils demonstrate waveguiding properties, the results indicate that covalent grafting of a fluorophore directly to a waveguide host mayAbstract : The chain length and branching of the organic backbone of poly(oxyalkylene)/siloxane ureasils can be used to control the placement and orientation of a covalently-grafted perylene, leading to tunable photoluminescence. Abstract : A series of organic–inorganic hybrid materials in which a perylene carboxdiimide-bridged triethoxysilane (PDI-Sil ) is covalently grafted to the siliceous domains of poly(oxyalkylene)/siloxane hybrids from the ureasil family has been synthesised (PDI-Sil -ureasils), with the aim of tailoring the optical properties towards their future application in luminescent solar concentrators (LSCs). Steady-state and time-resolved photoluminescence studies revealed that the ureasil host is able to isolatePDI-Sil, which inhibits the formation of aggregates. The ureasil also functions as an active host, with its intrinsic photoluminescence contributing to the optical properties of the hybrid material. Through strategic variation of the branching and molecular weight of the poly(oxyalkylene) backbone, it was shown that the efficiency of energy transfer from the ureasil host to thePDI-Sil can be modulated, which tunes the emission colour from pink to orange. The chain length, rather than the number of branches, on the poly(oxyalkylene) backbone was shown to influence the photoluminescence most significantly. Since ureasils demonstrate waveguiding properties, the results indicate that covalent grafting of a fluorophore directly to a waveguide host may provide an attractive route to more efficient LSCs. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 4:Issue 18(2016)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 4:Issue 18(2016)
- Issue Display:
- Volume 4, Issue 18 (2016)
- Year:
- 2016
- Volume:
- 4
- Issue:
- 18
- Issue Sort Value:
- 2016-0004-0018-0000
- Page Start:
- 4049
- Page End:
- 4059
- Publication Date:
- 2016-03-31
- Subjects:
- Materials -- Periodicals
Chemistry, Analytic -- Periodicals
Optical materials -- Research -- Periodicals
Electronics -- Materials -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/tc# ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5tc03952e ↗
- Languages:
- English
- ISSNs:
- 2050-7526
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1764.xml