DNA-based programming of quantum dot valency, self-assembly and luminescence

被引:1
作者
Tikhomirov, Grigory [1 ]
Hoogland, Sjoerd [2 ]
Lee, P. E. [1 ]
Fischer, Armin [2 ]
Sargent, Edward H. [2 ]
Kelley, Shana O. [1 ,3 ]
机构
[1] Univ Toronto, Leslie Dan Fac Pharm, Dept Pharmaceut Sci, Toronto, ON M5S 3M2, Canada
[2] Univ Toronto, Dept Elect & Comp Engn, Toronto, ON M5S 3G4, Canada
[3] Univ Toronto, Dept Biochem, Toronto, ON M5S 1A8, Canada
基金
美国国家卫生研究院;
关键词
NANOCRYSTALS; NANOPARTICLES; CRYSTALLIZATION; PHOTODETECTORS; NANOSTRUCTURES; ORGANIZATION; RESOLUTION; POLYMER; CELLS; GOLD;
D O I
10.1038/NNANO.2011.100
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The electronic and optical properties of colloidal quantum dots, including the wavelengths of light that they can absorb and emit, depend on the size of the quantum dots. These properties have been exploited in a number of applications including optical detection(1-3), solar energy harvesting(4,5) and biological research(6,7). Here, we report the self-assembly of quantum dot complexes using cadmium telluride nanocrystals capped with specific sequences of DNA. Quantum dots with between one and five DNA-based binding sites are synthesized and then used as building blocks to create a variety of rationally designed assemblies, including cross-shaped complexes containing three different types of dots. The structure of the complexes is confirmed with transmission electron microscopy, and photophysical studies are used to quantify energy transfer among the constituent components. Through changes in pH, the conformation of the complexes can also be reversibly switched, turning on and off the transfer of energy between the constituent quantum dots.
引用
收藏
页码:485 / 490
页数:6
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