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Near-Infrared Quantum Dot Emission Enhanced by Stabilized Self-Assembled J-Aggregate Antennas.
Freyria, Francesca S; Cordero, José M; Caram, Justin R; Doria, Sandra; Dodin, Amro; Chen, Yue; Willard, Adam P; Bawendi, Moungi G.
Afiliação
  • Freyria FS; Department of Chemistry, Massachusetts Institute of Technology , Cambridge, Massachusetts 02139, United States.
  • Cordero JM; Department of Chemistry, Massachusetts Institute of Technology , Cambridge, Massachusetts 02139, United States.
  • Caram JR; Department of Chemistry, Massachusetts Institute of Technology , Cambridge, Massachusetts 02139, United States.
  • Doria S; Department of Chemistry, Massachusetts Institute of Technology , Cambridge, Massachusetts 02139, United States.
  • Dodin A; European Laboratory for Non Linear Spectroscopy (LENS), Università di Firenze , Sesto Fiorentino, Florence, 50019 Italy.
  • Chen Y; Department of Chemistry, Massachusetts Institute of Technology , Cambridge, Massachusetts 02139, United States.
  • Willard AP; Department of Chemistry, Massachusetts Institute of Technology , Cambridge, Massachusetts 02139, United States.
  • Bawendi MG; Department of Chemistry, Massachusetts Institute of Technology , Cambridge, Massachusetts 02139, United States.
Nano Lett ; 17(12): 7665-7674, 2017 12 13.
Article em En | MEDLINE | ID: mdl-29148805
ABSTRACT
Enhancing photoluminescent emission (PL) in the near-infrared-infrared (NIR-IR) spectral region has broad applications from solar energy conversion to biological imaging. We show that self-assembled molecular dye J-aggregates (light-harvesting nanotubes, LHNs) can increase the PL emission of NIR PbS quantum dots (QDs) in both liquid and solid media more than 8-fold, promoted primarily by a long-range antenna effect and efficient Förster resonance energy transfer (FRET) from donor to acceptor. To create this composite material and preserve the optical properties of the nanocrystals, we performed an in situ ligand substitution followed by a functionalization reaction using click-chemistry. This resulted in PbS QDs soluble in an aqueous environment compatible with the molecular J-aggregates (LHNs). Theoretical and experimental results demonstrate that long-range diffusive exciton transport in LHNs enables efficient energy transfer to low concentrations of QDs despite there being no direct binding between molecular donors and QD acceptors. This suggests a broad application space for mixed light harvesting and photophysically active nanocomposite materials based on self-assembling molecular aggregates.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article