6533b873fe1ef96bd12d4ac0

RESEARCH PRODUCT

Acceptor Concentration Dependence of Förster Resonance Energy Transfer Dynamics in Dye–Quantum Dot Complexes

Thomas BaschéJosef WachtveitlLars DworakVictor V. MatylitskyTing Ren

subject

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 ChemistryPerylene

description

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 transfer is utilized for the determination of the energy transfer dynamics. Our time-resolved measurements demonstrate that an increase of the acceptor concentration accelerates the donor–acceptor energy transfer. Considering a Poisson distribution of acceptor molecules per quantum dot, the dependence of the energy tra...

https://doi.org/10.1021/jp409807x