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Silica Coating of Water-Soluble CdTe/CdS Core-Shell Nanocrystals by Microemulsion Method

机译:微乳液法制备水溶性CdTe / CdS核壳纳米晶的二氧化硅涂层

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We report a synthesis route to prepare CdTe/CdS core-shell nanoparticles (NPs) in aqueous solution. Using Te powder as tellurium source and Na2S as sulfur source, core-shell CdTe/CdS NPs were synthesized at 50 oC. UV-visible and Photoluminescence (PL) spectra are used to probe the effect of CdS passivation on the CdTe quantum dots. As the thickness of CdS shell increases, there is a red-shift in the optical absorption spectra, as well as the photoluminescence (PL) spectra. The broadening absorption peaks and PL spectra indicate that the size distributions of CdTe/CdS NPs widen increasingly with the increasing of CdS coverage. The PL spectra also show that the fluorescence intensity of CdTe QDs will increase when the particles are covered with CdS shell with ratio of S/Te less than 1.0, otherwise it will decrease if ratio of S/Te larger than 1.0. Furthermore, the (CdTe/CdS) @SiO2 particles are prepared by a water-in-oil microemulsion method at room temperature in which hydrolysis of tetraethyl orthosilicate leads to the formation of monodispersed silica nanospheres. The obtained (CdTe/CdS)@SiO2 particles show bright photoluminescence with their fluorescence intensity being enhanced 18.5% compared with that of CdTe NPs. TEM image shows that the diameter of these composite particles is 50 nm. These nanoparticles are suitable for biomarker applications since they are much smaller than cellular dimensions.
机译:我们报告了制备水溶液中的CdTe / CdS核壳纳米粒子(NPs)的合成途径。以Te粉为碲源,Na2S为硫源,在50 oC下合成了核壳型CdTe / CdS NPs。紫外可见光和光致发光(PL)光谱用于探测CdS钝化对CdTe量子点的影响。随着CdS壳厚度的增加,光吸收光谱以及光致发光(PL)光谱都会发生红移。吸收峰和PL光谱的增宽表明,CdTe / CdS NPs的粒径分布随着CdS覆盖率的增加而越来越宽。 PL光谱还表明,当颗粒被Sd / Te比小于1.0的CdS壳覆盖时,CdTe量子点的荧光强度将增加,否则当S / Te比大于1.0时,荧光强度将降低。此外,在室温下通过油包水微乳液法制备(CdTe / CdS)@SiO 2颗粒,其中原硅酸四乙酯的水解导致形成单分散的二氧化硅纳米球。与CdTe NP相比,所获得的(CdTe / CdS)@ SiO2颗粒显示出明亮的光致发光,其荧光强度提高了18.5%。 TEM图像显示这些复合颗粒的直径为50nm。这些纳米粒子比细胞尺寸小得多,因此适用于生物标记物应用。

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