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树枝状大分子纳米复合材料中CdTe微晶的尺寸可调性及尺寸分布的温度依赖性聚焦

Size tunablity of CdTe crystallites in dendrimer nanocomposites and temperature dependent focusing of size distribution.

作者信息

Ghosh Srabanti, Priyam Amiya, Chatterjee Anindita, Saha Abhijit

机构信息

UGC-DAE Consortium for Scientific Research, Kolkata Centre, III/LB-8, Bidhananagar, Kolkata 700098, India.

出版信息

J Nanosci Nanotechnol. 2008 Nov;8(11):5952-7.

PMID:19198331
Abstract

CdTe/Dendrimer nanocomposites have been synthesized for the first time in aqueous and nonaqueous media using PAMAM dendrimer (Generation 5.0). The average size of the as-prepared nanocomposites, as determined from dynamic light scattering (DLS) measurements, was found to be typically 182 nm and 23 nm in water and methanol, respectively under identical conditions of temperature (5 degrees C) and reagent ratio (Cd2+:Te2-, 1:0.5). The size of CdTe NPs within the nanocomposites, was found to be 3.1 and 2.8 nm for the aforementioned samples determined from optical absorption spectra using tight binding approximation. The NPs possess good degree of cystallinity as discernible from the lattice fringes in high-resolution transmission electron microscopic (HRTEM). Transmission electron microscopic (TEM) image and the cubic crystal phase was ascertained from the small area electron diffraction (SAED) pattern. Analysis of FTIR data suggests that CdTe NPs are bound to the surface amine groups as well as -NHCO- moieties lying in the interior of dendrimer structure. The present work demonstrates how the quality of the CdTe NPs formed within the dendrimer matrix can be nicely tuned by varying the parameters, namely, temperature, molar ratio of Cd2+: Te2- and pH. Changing of Cd2+: Te2- ratio of 1:1 to 1:0.5, decreased the average particle size from 5.0 nm to 3.4 nm with concomitant narrowing of size distribution by approximately 35% at 10 degrees C. On lowering down the synthesis temperature (25 degrees C-->5 degrees C), the average particle size remained unaffected while the size distribution became sharply focused. However, the extent of focusing was found to be more in methanol (40%) than that in water (30%).

摘要

首次使用聚酰胺-胺(PAMAM)树枝状大分子(第5.0代)在水性和非水性介质中合成了碲化镉/树枝状大分子纳米复合材料。在相同的温度(5摄氏度)和试剂比例(Cd2+:Te2-,1:0.5)条件下,通过动态光散射(DLS)测量确定,所制备的纳米复合材料在水中和甲醇中的平均尺寸分别通常为182纳米和23纳米。使用紧密束缚近似从光学吸收光谱确定,上述样品中纳米复合材料内碲化镉纳米颗粒的尺寸分别为3.1纳米和2.8纳米。从高分辨率透射电子显微镜(HRTEM)中的晶格条纹可以看出,纳米颗粒具有良好的结晶度。通过小面积电子衍射(SAED)图案确定了透射电子显微镜(TEM)图像和立方晶相。傅里叶变换红外光谱(FTIR)数据分析表明,碲化镉纳米颗粒与树枝状大分子结构内部的表面胺基以及-NHCO-部分结合。本工作展示了如何通过改变温度、Cd2+:Te2-的摩尔比和pH值等参数,很好地调节在树枝状大分子基质中形成的碲化镉纳米颗粒的质量。在10摄氏度下,将Cd2+:Te2-的比例从1:1变为1:0.5,平均粒径从5.0纳米减小到3.4纳米,同时粒径分布变窄约35%。降低合成温度(25摄氏度→5摄氏度)时,平均粒径不受影响,而粒径分布变得更加集中。然而,发现甲醇中的集中程度(40%)比水中的(30%)更高。

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