CdTe Quantum Dots/Layered Double Hydroxide Ultrathin Films with Multicolor Light Emission via Layer-by-Layer Assembly

被引:85
|
作者
Liang, Ruizheng [1 ]
Xu, Simin [1 ]
Yan, Dongpeng [1 ]
Shi, Wenying [1 ]
Tian, Rui [1 ]
Yan, Hong [1 ]
Wei, Min [1 ]
Evans, David G. [1 ]
Duan, Xue [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
ION-EXCHANGE INTERCALATION; EMITTING-DIODES; ENERGY-TRANSFER; ANION-EXCHANGE; OPTICAL GAIN; NANOCRYSTALS; LUMINESCENCE; DOTS; ELECTROLUMINESCENCE; NANOPARTICLES;
D O I
10.1002/adfm.201201367
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Quantum dots (QDs) luminescent films have broad applications in optoelectronics, solid-state light-emitting diodes (LEDs), and optical devices. This work reports the fabrication of multicolor-light-emitting ultrathin films (UTFs) with 2D architecture based on CdTe QDs and MgAl layered double hydroxide (LDH) nanosheets via the layer-by-layer deposition technique. The hybrid UTFs possess periodic layered structure, which is verified by X-ray diffraction. Tunable light emission in the red-green region is obtained by changing the particle size of QDs (CdTe-535 QDs and CdTe-635 QDs with green and red emision respectively), assembly cycle number, and sequence. Moreover, energy transfer between CdTe-535 QDs and CdTe-635 QDs occurs based on the fluorescence resonance energy transfer (FRET), which greatly enhances the fluorescence efficiency of CdTe-635 QDs. In addition, a theoretical study based on the Forster theory and molecular dynamics (MD) simulations demonstrates that CdTe QDs/LDH UTFs exhibit superior capability of energy transfer owing to the ordered dispersion of QDs in the 2D LDH matrix, which agrees well with the experimental results. Therefore, this provides a facile approach for the design and fabrication of inorganic-inorganic luminescent UTFs with largely enhanced luminescence efficiency as well as stability, which can be potentially applied in multicolor optical and optoelectronic devices.
引用
收藏
页码:4940 / 4948
页数:9
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