Synthesis and optical properties of water-soluble CdTe1-xSex quantum dots with ultra-long fluorescence lifetime

被引:19
|
作者
Han, Zhizhong [1 ]
Ren, Lili [2 ]
Chen, Li [1 ]
Luo, Min [1 ]
Pan, Haibo [2 ,3 ]
Li, Chunyan [1 ]
Chen, Jinghua [1 ]
机构
[1] Fujian Med Univ, Sch Pharm, Fuzhou 350122, Fujian, Peoples R China
[2] Fuzhou Univ, Coll Chem, Fuzhou 350116, Fujian, Peoples R China
[3] Fuzhou Univ, Fujian Key Lab Med Instrument & Pharmaceut Techno, Fuzhou 350116, Fujian, Peoples R China
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
CdTe1-xSex; Quantum dots; Composition control; Photoluminescence; Fluorescence lifetime; Water-soluble; SOLAR-CELLS; BAND-GAP; NANOCRYSTALS; ENERGY; SHELL; ZNS;
D O I
10.1016/j.jallcom.2016.12.365
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Water-soluble ternary-alloyed CdTe1-xSex quantum dots (QDs) have been synthesized via a simple one pot approach in aqueous phase. The as-prepared CdTe1-xSex QDs show good crystallinity, excellent monodispersity, and a narrow size distribution with average size of 3.0 nm. Lattice parameters and band gaps of the ternary-alloyed CdTe1-xSex (0 <= x < 1) QDs are regulated respectively in linear and quadratic relationships with the Se content (x). By tuning composition, the photoluminescence (PL) emission wavelength of CdTe1-xSex can cover from 528.9 to 689.3 nm, and gradually moved to longer wavelengths with a decrease content of Se (x). The lifetime of CdTe1-xSex QDs is decreased gradually with the Se content (x) augment, attributing to the decreasing lattice spacing resulting from substitution of the larger Te atoms with the smaller Se atoms, bringing about a incremental plasmonic coupling effect at smaller inter-lattice fluorophore distance. However, the as-prepared CdTe1-xSex QDs (0 <= x < 1) have significantly longer fluorescence lifetimes of >80 ns with the maximum lifetime up to 174.64 ns. The longer life is good for the application of photoelectric conversion, fluorescent biomedical imaging and detecting. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:216 / 221
页数:6
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