0000000000388328

AUTHOR

Ting Ren

showing 4 related works from this author

A Simple and Versatile Route to Stable Quantum Dot−Dye Hybrids in Nonaqueous and Aqueous Solutions

2008

Hybrid systems consisting of core/shell semiconductor quantum dots (QDs) and organic rylene dyes have been prepared and characterized. Complex formation is mediated by bidentate carboxylate moieties covalently linked to the dye molecules. The complexes were very stable with respect to time (at least months), dilution (sub nM), and precipitation. After preparation in organic solvent, complexes could be easily transferred into water. The strong quenching of QD emission by the dye molecules (transfer efficiencies up to 95%) was satisfactorily modeled by an FRET process. Single complexes immobilized in thin polymer films were imaged by confocal fluorescence microscopy.

chemistry.chemical_classificationAqueous solutionQuenching (fluorescence)Inorganic chemistryGeneral ChemistryPolymerBiochemistryCatalysischemistry.chemical_compoundColloid and Surface ChemistryFörster resonance energy transferchemistryCovalent bondQuantum dotMoleculeCarboxylateJournal of the American Chemical Society
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Synthesis and Spectroscopic Properties of Silica−Dye−Semiconductor Nanocrystal Hybrid Particles

2010

We prepared silica-dye-nanocrystal hybrid particles and studied the energy transfer from semiconductor nanocrystals (= donor) to organic dye molecules (= acceptor). Multishell CdSe/CdS/ZnS semiconductor nanocrystals were adsorbed onto monodisperse Stöber silica particles with an outer silica shell of thickness 2-23 nm containing organic dye molecules (Texas Red). The thickness of this dye layer has a strong effect on the energy transfer efficiency, which is explained by the increase in the number of dye molecules homogeneously distributed within the silica shell, in combination with an enhanced surface adsorption of nanocrystals with increasing dye amount. Our conclusions were underlined by…

DispersityTexas RedBinary compoundNanotechnologychemistry.chemical_compoundAdsorptionMicroscopy Electron TransmissionQuantum DotsFluorescence Resonance Energy TransferElectrochemistryNanotechnologyMoleculeGeneral Materials ScienceColoring AgentsSpectroscopySurfaces and InterfacesSilicon DioxideCondensed Matter PhysicsAcceptorModels ChemicalSemiconductorsXantheneschemistryChemical engineeringNanocrystalSpectrophotometryNanoparticlesParticleSpectrophotometry UltravioletAdsorptionMonte Carlo MethodLangmuir
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Water-soluble, cyclodextrin-functionalized semiconductor nanocrystals: Preparation and pH-dependent aggregation and emission properties

2009

Abstract Using peramino-functionalized β-cyclodextrin molecules for phase.transfer of hydrophobic CdSe multishell nanocrystals into water, we obtained hydrophilic nanoparticles with high quantum yield (up to 50%). At pH > 9, the aqueous solution of these nanocrystals remained stable for several months. The nanoparticles showed a strong influence of the pH of the aqueous solution on the emission of the nanocrystals: the quantum yield varied reversible from ∼10% at pH=6 to ∼50% at pH=14, an effect which according to particle size characterization by dynamic light-scattering and asymmetric flow field-flow fractionation has mainly been attributed to reversible partial aggregation of the hydroph…

chemistry.chemical_classificationAqueous solutionPhotoluminescenceCyclodextrinInorganic chemistryBiophysicsQuantum yieldNanoparticleGeneral ChemistryCondensed Matter PhysicsBiochemistryAtomic and Molecular Physics and OpticschemistryNanocrystalChemical engineeringMoleculeParticle sizeJournal of Luminescence
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Acceptor Concentration Dependence of Förster Resonance Energy Transfer Dynamics in Dye–Quantum Dot Complexes

2014

The dynamics of the photoinduced Forster resonance energy transfer (FRET) in a perylene diimide–quantum dot organic–inorganic hybrid system has been investigated by femtosecond time-resolved absorption spectroscopy. The bidentate binding of the dye acceptor molecules to the surface of CdSe/CdS/ZnS multishell quantum dots provides a well-defined dye-QD geometry for which the efficiency of the energy transfer reaction can be easily tuned by the acceptor concentration. In the experiments, the spectral characteristics of the chosen FRET pair facilitate a selective photoexcitation of the quantum dot donor. Moreover, the acceptor related transient absorption change that occurs solely after energy…

Physics::Biological PhysicsAbsorption spectroscopyChemistryCondensed Matter::Mesoscopic Systems and Quantum Hall EffectPhotochemistryAcceptorSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPhotoexcitationCondensed Matter::Materials Sciencechemistry.chemical_compoundGeneral EnergyFörster resonance energy transferQuantum dotChemical physicsUltrafast laser spectroscopyMoleculePhysics::Chemical PhysicsPhysical and Theoretical ChemistryPeryleneThe Journal of Physical Chemistry C
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