Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/53290

TítuloHigh fluorescent water soluble CdTe quantum dots—a promising system for light harvesting applications
Autor(es)de Sá, Arsénio
Moura, Isabel
Abreu, Ana S.
Oliveira, Manuel António Sousa Cortez Gonçalves
Ferreira, Miguel F.
Machado, A. V.
Palavras-chaveAmphiphilic polymer
RAFT polymerization
Water soluble quantum dots
Enhanced photoluminescence
Polymer-coated QDs
Data2017
EditoraSpringer
RevistaJournal of Nanoparticle Research
Resumo(s)The entrapment of quantum dots (QDs) in the inner part of micelles formed by surfactant polymers is a powerful methodology to prepare stable and photoluminescent core nanoparticles with enhanced optical properties. These features are crucial for the application of QDs in the design of hybrid assemblies for light harvesting applications, where energy transfer processes are required. The present work was focused on the synthesis of a surfactant homopolymer, poly (acrylic acid) (PAA) macroRAFT, to be used as a stabilizer of hydrophobic cadmium telluride (CdTe) QDs in aqueous solution. PAA macroRAFT was synthesized by reversible addition-fragmentation chain-transfer (RAFT) polymerization in a single chemical reaction. Its micelles were used to entangle and entrap hydrophobic CdTe QDs, with different molar ratio of polymer and QDs. The morphology and optical properties of the entrapped QDs were determined. The results showed that PAA macroRAFT is able to form micelles with a critical micelle concentration of 2.08 mg/mL. It was also noticed that the molar ratio of polymer and QDs have high influence on the QDs' morphology and their optical properties. The QDs' photoluminescence quantum yield was enhanced approximately 23% upon their entrapment in PAA macroRAFT micelles, using 60 equivalents of polymer. Moreover, while in solution, QDs are well-dispersed, having a 3.5 nm diameter, upon being entrapped in the micelles, tend to form clusters with a size around 100 nm.
TipoArtigo
URIhttps://hdl.handle.net/1822/53290
DOI10.1007/s11051-017-3872-0
ISSN1388-0764
e-ISSN1572-896X
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