Poly(4-vinylpyridine) Coated CdTe Core/Shell Quantum Dots

2009 ◽  
Vol 60-61 ◽  
pp. 114-118 ◽  
Author(s):  
Zhao Dai ◽  
Ping Li ◽  
Ji Mei Zhang ◽  
Shi Chao Xu ◽  
Ning Guo ◽  
...  

A kind of novel quantum dots (QDs) with poly(4-vinylpyridine) (PVPy) as shell and CdTe QDs as core was presented in this work. This core/shell ODs can conjugate DNA easily because the surface pyridyl exist on QDs, and which has potential application in DNA biosensors field. CdTe QDs were prepared in aqueous solution with 3-mercaptopropionic acid (MPA) as stabilizer. It was found that the fluorescent intensity of QDs was depended the reflux time. Following the increase of reflux time, the fluorescent intensity of QDs reached the maximum at 10 h with about 10 nm in diameters. And the fluorescent intensity of QDs was also increased. When the reflux time was 10 h, the diameter of QDs would increase to about 10 nm. After adjusted the pH of QDs solution system to 7.0, the MPA stabled QDs were purified by ultracentrifugation and freeze-drying respectively. The polymerization was performed in water when 4-vinylpyridine (VPy) used as monomer, N,N’-methylene-bisacrylamide (MBAAm) as crosslinker, potassium persulphate (PPS) as initiator and MPA stabled QDs as seeds. The surface carboxyl of MPA on QDs could promote the form of PVPy coated CdTe QDs. It was shown that the fluorescent intension of core/shell QDs was decreased following the polymerization and the diameter of QDs could increase to 20-30 nm.

2013 ◽  
Vol 372 ◽  
pp. 115-118
Author(s):  
Meng Meng Song ◽  
Wen Juan Guo ◽  
Zhao Dai ◽  
Kai Li Qiu ◽  
Jun Fu Wei

Fluorescent DNA probes based on the fluorescence resonance energy transfer (FRET) were presented in this paper when AuNPs were as the energy acceptors and CdTe quantum dots and CdTe/SiO2 core/shell nanoparticles were as the energy acceptors, respectively. The DNA probes were prepared when energy donors and acceptors were conjugated with two single-stranded complementary oligonucleotides and hybridized with each other and the fluorescent intensity of probes could be decreased. The quenching efficiency of DNA probe was about 67 % when CdTe QDs were as the energy donors, while that of DNA probe was about 75 % when CdTe/SiO2 fluorescent core/shell nanoparticles were as the energy acceptors, which indicated that CdTe/SiO2 core/shell nanoparticles were suitable donors compared with CdTe QDs in DNA probe field.


2015 ◽  
Vol 132 ◽  
pp. 650-654 ◽  
Author(s):  
Qingyao Wang ◽  
Song Li ◽  
Jianlei Qiao ◽  
Rencheng Jin ◽  
Yifu Yu ◽  
...  

2020 ◽  
Vol 20 (9) ◽  
pp. 5478-5485
Author(s):  
Cong Xie ◽  
Yubin Zhao ◽  
Yuxiang Song ◽  
Yingjie Liu ◽  
Yaya Wang ◽  
...  

Compared with conventional semiconductor quantum dots, hybrid SiO2 coated CdTe QDs exhibited high stability, long fluorescent lifetime, high photoluminescence quantum yields, and well biocompatibility. In this paper, CdTe QDs with tunable PL from green to red emitting were prepared by an aqueous synthesis. A sol–gel process resulted in CdTe QDs coated with a hybrid SiO2 shell contained CdS-like clusters to obtain red-shifted PL spectra, increased PL efficiency and high stability. The clusters were formed by the reaction of Cd2+ and S2− ions generated via the decomposition of thioglycolic acid. The clusters around CdTe cores created a core–shell structure which is very similar with traditional semiconductor core–shell QDs. After being coated with a hybrid SiO2 shell, the PL of green-emitting naked CdTe QDs was red-shifted largely (~30 nm) while the PL of yellowemitting CdTe QDs revealed a small red-shifted (~20 nm). Furthermore, The PL of red-emitting naked CdTe QDs was red-shifted much small (less than 10 nm). This phenomenon is ascribed to the change of band gap of CdTe cores with sizes. The red-shift of PL spectra is attributed to the CdS-like clusters around the core rather than the thickness of the hybrid SiO2 shell.


2017 ◽  
Vol 90 (1) ◽  
pp. 52-58 ◽  
Author(s):  
Taichi Watanabe ◽  
Kohji Takahashi ◽  
Kunio Shimura ◽  
Hang-Beom Bu ◽  
Kim Hyeon-Deuk ◽  
...  

2011 ◽  
Vol 306-307 ◽  
pp. 1350-1353 ◽  
Author(s):  
Juan Juan Lu ◽  
Shen Guang Ge ◽  
Fu Wei Wan ◽  
Jing Hua Yu

This paper describes the synthesis of CdTe and CdTe/CdS core-shell quantum dots (QDs) in aqueous solution. The quantum dots are prepared by using thioglycolic acid (TGA) as stabilizers. The synthesis procedure is simple and controllable. Different sized CdTe QDs with tuned PL wavelengths from 550 to 640 nm was synthesized by controlling reaction time within 5 h in aqueous solutions at a temperature of 100 °C. We also investigated the influence of precursor Cd/Te molar ratio for the prepared QDs. It was showed that the core-shell CdTe/CdS QDs have larger photoluminescence (PL) emission intensity than the original CdTe QDs. The synthesized core-shell CdTe/ZnS QDs have high quality, water-soluble and will be useful in applications of biolabeling, biosensing, and imaging.


ChemPhysChem ◽  
2016 ◽  
Vol 17 (5) ◽  
pp. 670-674 ◽  
Author(s):  
Loredana Protesescu ◽  
Tanja Zünd ◽  
Maryna I. Bodnarchuk ◽  
Maksym V. Kovalenko

2009 ◽  
Vol 60-61 ◽  
pp. 165-169 ◽  
Author(s):  
Shi Chao Xu ◽  
Cui Cui Yao ◽  
Ji Mei Zhang ◽  
Zhao Dai ◽  
Guo Zheng ◽  
...  

Core-shell quantum dots are colloidal particles consisting of a semiconductor core and a shell material as an outer coating layer. It can be utilized to develop sensitive methods for the detection of specific biological entities, such as microbial species, their transcription products, and single genes etc. The goal of current research is to synthesize CdTe and core-shell CdTe/ZnS quantum dots (QDs) with an improved process, and to investigate their properties. Well-dispersed CdTe core was prepared in aqueous phase with using 3-mercaptopropionic acid (MPA) as stabilizer under conditions of pH 9.1, temperature of 100 °C, refluxing for 6h, and mol ratio of Cd2+/Te2-/MPA is 1:0.5:2.4. Average size of 8 nm CdTe core was conformed via transmission electron microscopy (TEM). Core-shell CdTe/ZnS QDs were then synthesized to improve the optical properties and biocompatibility of CdTe core. Various conditions were researched to obtain the core-shell QDs with the best optical properties, such as quantum yields, fluorescence intensity etc. The results indicated that the core-shell qualified CdTe/ZnS was prepared under conditions of pH 9.0, temperature of 45 °C, refluxing for 1h, and mol ratio of CdTe/S2-/Zn2+ is 4/1/1. CdTe/ZnS with average size of 10 nm were achieved and conformed via TEM. Moreover, red shift of a maximum emission wavelength from 547 nm of CdTe to 587 of CdTe/ZnS was observed via fluorescence spectrum (FS), which inferred the growth of QDs and formation of ZnS shells. The achieved ZnS shell make CdTe core less toxic and more biocompatible, it will be useful in biological labeling, diagnostic process and biosensing system based on fluorescence resonance energy transition (FRET).


Author(s):  
Nguyen Xuan Ca ◽  
Nguyen Thi Hien

The CdSe, type-II CdSe/CdTe core/shell and type-II/type-I CdSe/CdTe/ZnS core/shell/shell  quantum dots (QDs) were successfully synthesized in a noncoordinating solvent. The phonon characterizations, optical properties and structures of the synthesized QDs were characterized by Raman scattering (RS) spectra, photoluminescence (PL) spectroscopy, PL-decay lifetime, absorption spectroscopy (Abs), and X-ray diffraction (XRD). The growth of QDs was monitored by using RS, which demonstrated the formation of correct of the core/shell and core/shell/shell structures. Observation results from XRD reveal that all QDs crystallize in the cubic phase with zinc-blende structure. The typical characteristics of spatially indirect recombination for type-II QDs were observed through Abs and PL spectroscopy. The ZnS shell significantly enhanced the PL quantum yeild (QY), the optical durability, the chemical stability and separating CdSe/CdTe QDs from the surroundings. The effect of excitation power on the PL properties of the CdSe core,  CdSe/CdTe and CdSe/CdTe/ZnS QDs has been investigated.


2007 ◽  
Vol 92 ◽  
pp. 012039
Author(s):  
T-M Liu ◽  
J-Y Lu ◽  
C-C Kuo ◽  
Y-C Wen ◽  
C-W Lai ◽  
...  

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