Nanotubular J-Aggregates and Quantum Dots Coupled for Efficient Resonance Excitation Energy Transfer

被引:38
|
作者
Qiao, Yan [1 ,2 ]
Polzer, Frank [1 ]
Kirmse, Holm [1 ]
Steeg, Egon [1 ]
Kuehn, Sergei [3 ]
Friede, Sebastian [3 ]
Kirstein, Stefan [1 ]
Rabe, Juergen P. [1 ,2 ]
机构
[1] Humboldt Univ, Dept Phys, D-12489 Berlin, Germany
[2] Humboldt Univ, IRIS Adlershof, D-12489 Berlin, Germany
[3] Nichtlineare Opt & Kurzzeitspektroskopie Forsch V, Max Born Inst, D-12489 Berlin, Germany
关键词
Forster resonance energy transfer (FRET); organic-inorganic hybrid system; amphiphilic cyanine dye; semiconductor; CdTe; self-assembly; light harvesting; ORGANIC/INORGANIC SEMICONDUCTOR NANOSTRUCTURES; CARBOCYANINE DYE; NANOCRYSTALS; FLUORESCENCE; MIGRATION; SPECTRA; POLYMER; SURFACE; FILMS;
D O I
10.1021/nn506095g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Resonant coupling between distinct excitons in organic supramolecular assemblies and inorganic semiconductors is supposed to offer an approach to optoelectronic devices. Here, we report on colloidal nanohybrids consisting of self-assembled tubular J-aggregates decorated with semiconductor quantum dots (QDs) via electrostatic self-assembly. The role of QDs in the energy transfer process can be switched from a donor to an acceptor by tuning its size and thereby the excitonic transition energy while keeping the chemistry unaltered. QDs are located within a close distance (<4 nm) to the J-aggregate surface, without harming the tubular structures and optical properties of J-aggregates. The close proximity of J-aggregates and QDs allows the strong excitation energy transfer coupling, which is around 92% in the case of energy transfer from the QD donor to the J-aggregate acceptor and approximately 20% in the reverse case. This system provides a model of an organicinorganic light-harvesting complex using methods of self-assembly in aqueous solution, and it highlights a route toward hierarchical synthesis of structurally well-defined supramolecular objects with advanced functionality.
引用
收藏
页码:1552 / 1560
页数:9
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