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1.
生物相容的高荧光CdTe量子点的合成和表征   总被引:2,自引:0,他引:2  
用硫普罗宁(tiopronin,TP)作为稳定剂,在水相中合成了荧光发射波长可调的高荧光CdTe量子点。本文详细地研究了稳定剂与Cd之比和pH值等实验条件对CdTe纳米粒子体系的荧光量子产率的影响。在pH=11.3回流2 h,纳米粒子体系在537 nm波长处的荧光量子产率达到了66%。通过控制实验条件,合成了各种尺寸的CdTe量子点,荧光发射光谱在504~602 nm范围连续可调。分别用X射线光电子能谱(XPS)、透射电子显微镜(TEM)、X射线衍射(XRD)、红外吸收光谱(FTIR)表征了CdTe粒子的分散性、形貌和晶型。溶血实验显示,这些由硫普罗宁稳定的CdTe量子点几乎不发生溶血作用(溶血率低于5%),具有良好的生物相容性。  相似文献   

2.
以亚碲酸钠为碲源,硼氢化钠为还原剂,一步合成了巯基丁二酸(MSA)稳定的CdTe量子点.研究了反应液pH值、镉与碲的摩尔比及镉与巯基丁二酸的摩尔比等实验条件对CdTe量子点体系荧光量子产率的影响,并用荧光光谱、X射线粉末衍射及透射电子显微镜等对其进行了表征.结果表明,CdTe量子点具有闪锌矿结构,形貌呈球状;在pH=1...  相似文献   

3.
用L-半胱氨酸(L-cysteine)作为稳定剂,以制备的CdTe量子点为核模板,水相合成了具有近红外发光的Ⅱ型核壳CdTe/CdSe半导体量子点。实验考察了合成温度,核模板的尺寸和组分比等因素对合成高质量的CdTe/CdSe量子点的影响。用紫外-可见吸收和荧光光谱研究了合成的量子点的光学性质。在优化的合成条件下,荧光发射光谱在586~753nm范围连续可调,荧光量子产率高达68%;通过X-射线衍射(XRD),X射线光电子能谱(XPS)和透射电镜(TEM)对合成的Ⅱ型核壳CdTe/CdSe量子点进行了结构和形貌表征。  相似文献   

4.
在水相中合成高发光性能的CdTe量子点,研究以巯基乙酸(TGA)为稳定剂对CdTe表面进行修饰,制备在水中分散性良好的纳米晶,通过对CdTe量子点合成反应条件的摸索,掌握了其合成的反应规律.同时用紫外分光光度计、荧光分光光度计和透射电子显微镜对其进行了表征.结果表明,回流时间、n(Cd2+):n(HTe-)、反应物浓度、TGA用量、反应体系pH值,对纳米晶的光学性质具有显著影响.回流2 h制得的CdTe纳米粒子直径约为5 nm,其发射峰窄且对称,表现出良好稳定的光学性质.  相似文献   

5.
以巯基丙酸(RSH)为稳定剂,采用水相法合成了功能性CdTe纳米晶,并通过X射线衍射(XRD)和透射电镜(TEM)对其粒度和形貌进行表征。建立了一种以水溶性CdTe量子点作为荧光探针测定DNA的方法,当DNA浓度为0.2~40μmol.dm-3时,荧光强度与DNA浓度呈良好的线性关系,检测限为80nmol.dm-3,11次重复测定含有5.6μmol.dm-3的小牛胸ctDNA得到的相对标准偏差为3.4%。考察了CdTe量子点浓度、pH值、温度及作用时间等因素对DNA荧光强度的影响。研究发现CdTe纳米粒子与DNA之间存在强烈的相互作用,量子点的荧光猝灭与DNA浓度呈线性关系;作用机理研究表明,CdTe纳米粒子与DNA之间存在静电相互作用,且DNA对CdTe纳米粒子的猝灭为动态猝灭过程。  相似文献   

6.
提出了一种以水热法合成巯基乙胺稳定的CdTe量子点的简单制备路线. 在优化的反应条件下, 产物的荧光量子效率最高达到19.7%, 接近已报道的其它方法的2倍. 考察了反应条件对产物的荧光性能的影响及产物在不同pH溶液中的稳定性.  相似文献   

7.
由共沉淀法和Stober法制备了伯胺基功能化SiO2稳定的Fe3O4磁性纳米粒子Fe3O4@SiO2-NH2;Fe3O4@SiO2-NH2与二异氰酸酯及咪唑阳离子二醇、聚乙二醇的反应使其表面形成阳离子型聚氨酯稳定层;通过阳离子型聚氨酯与CdTe量子点表面修饰的巯基乙酸间的电荷相互作用,制备得到了Fe3O4/CdTe/聚氨酯纳米复合物.用X射线衍射(XRD)、红外吸收光谱(FTIR)、热重分析(TGA)、透射电子显微镜(TEM)、磁强计(VSM)、紫外吸收光谱(UV)、荧光发射光谱(PL)表征了该纳米复合物的结构与性能.结果表明,CdTe量子点均匀地分散在Fe3O4@SiO2磁性纳米粒子周围,所得纳米复合物在溶剂中分散均匀,不团聚,且具有超顺磁性,并保持了CdTe量子点的荧光性能.  相似文献   

8.
胃蛋白酶对CdTe纳米粒子的表面修饰及分析应用   总被引:1,自引:0,他引:1  
以巯基乙酸为稳定剂和表面修饰剂, 在有机相中合成了平均粒径为3 nm左右的CdTe纳米粒子, 用胃蛋白酶改变纳米粒子的表面修饰状态并研究其系列特性. CdTe纳米粒子在320 nm处有强的紫外吸收, 在524.8 nm处有荧光发射. 经胃蛋白酶对其表面修饰后, 紫外吸收峰位不变, 但吸光强度升高, 荧光峰位蓝移至467.2 nm, 荧光强度降低. 温度、pH值及离子强度均对表面修饰产生影响. 在最佳实验条件下, 胃蛋白酶质量浓度在4—40 mg/L范围内与荧光降低值之间呈线性关系, 检测限(3σ)为0.28 mg/L(n=10), 该方法已被用于人体胃液胃蛋白酶的测定.  相似文献   

9.
水溶性CdTe量子点的合成及影响因素研究   总被引:1,自引:0,他引:1  
本文以巯基乙酸(TGA)为稳定剂,在水相中合成了高荧光CdTe量子点.其荧光发射波长在507 ~ 628nm范围内可调,最窄半峰宽37 nm,粒径约3.4nm,量子产率达42.1%.本实验在固定前躯体配比不变的情况下,考察了前躯体中镉离子的浓度、pH及回流时间对CdTe生长的影响.并用透射电子显微镜(TEM),荧光分光光度计(FS),X射线衍射仪(XRD)等手段对制备的量子点进行了表征.结果表明:CdTe量子点的尺寸随回流时间而增长;反应的pH对量子点的荧光强度有显著影响;镉离子的浓度越大,量子点的生长速度越快,荧光强度却随之降低.  相似文献   

10.
以3-巯基丙酸(MPA)和柠檬酸钠为稳定剂,Na2TeO3为碲源,利用水热法成功制备了从绿色到近红外发射的CdTe量子点,并详细探讨了影响CdTe量子点体系的荧光发射波长和量子产率的因素,如反应前驱液的pH值,反应物的浓度比和反应时间等实验条件.分别用X射线粉末衍射、透射电镜、紫外-可见光谱和荧光光谱对CdTe量子点进行了表征.  相似文献   

11.
Highly luminescent thioglycolic acid-capped CdTe-based core/shell quantum dots (QDs) were synthesized through encapsulating CdTe QDs in various inorganic shells including CdS, ZnS and CdZnS. CdTe/CdS core/shell QDs exhibited a significant redshift of emission peaks (a maximum emission peak of 652 nm for the core/shell QDs and 575 nm for CdTe cores) with increasing shell thickness. In contrast, the redshift of photoluminescence (PL) peak wavelength of CdTe/ZnS QDs was less than 15 nm. The PL peak wavelengths of the core/shell QDs depended strongly on core size and shell thickness. The PL quantum yields (QYs) of the CdTe/CdS core/shell QDs are up to 67 % while that of CdTe/ZnS core/shell QDs is 45 %. A composite CdZnS shell made CdTe cores a high PL QY up to 51 % and broadly adjusted PL spectra (a maximum PL peak wavelength of 664 nm). The epitaxial growth of the shell was confirmed by X-ray powder diffraction analysis and luminescence decay experiments. Because of high PL QYs, tunable PL spectra, and low toxicity from a ZnS surface layer, CdTe/CdZnS core/shell QDs will be great potential for bioapplications.  相似文献   

12.
以3-巯基丙酸(MPA)为稳定剂,采用水相合成法制备了从绿色到近红外发射的CdTe量子点。系统研究了反应液pH值、镉和碲的物质的量之比及镉和3-巯基丙酸的物质的量之比等实验条件对CdTe量子点体系的发射波长和荧光量子产率的影响。在pH值为10.5,且nCd2+∶nTe2-∶nMPA=1∶0.05∶1.1的条件下,回流0.5 h,CdTe量子点体系在569 nm波长处的荧光量子产率达到30.8%;在7 h的回流时间内,制备的量子点的波长覆盖范围为525~730 nm。分别用X射线粉末衍射、透射电镜和红外光谱对CdTe量子点的晶体结构、形貌及表面基团进行表征。  相似文献   

13.
As one of the most popular nanocrystals (NCs), aqueous CdTe NCs have very weak green emission under conventional synthesis conditions. In this work, we report the first example of blue‐emitting CdTe NCs directly synthesized in aqueous solution by slowing down the growth rate after nucleation. The key for the synthesis is the optimization of NC growth conditions, namely pH range of 7.5 to 8.5, TGA/Cd ratio of 3.6, Cd/Te ratio of 10, and Te concentration of 2×10?5 mol/L, to get a slow growth rate after nucleation. The as‐prepared blue‐emitting CdTe NCs have small size (as small as 1.9 nm) and bright emission [with 4% photoluminescence quantum yield (PL QY) at 486 nm and 17% PLQY at 500 nm]. Transmission electron microscopy (TEM) images of the as‐prepared CdTe show monodispersed NCs which exhibit cubic zinc blend structure. Moreover, time‐resolved PL decay and X‐ray photoelectron spectroscopy (XPS) results show the as‐prepared NCs have better surface modification by ligand, which makes these luminescent small CdTe NCs have higher photoluminescence quantum yield, compared with NCs synthesized under conventional conditions.  相似文献   

14.
Chemically reduced bovine serum albumin (BSA) has been used to modify the surface of water-soluble CdTe quantum dots (QDs). It is demonstrated that the denatured BSA (dBSA) can be conjugated to the surface of CdTe QDs and thereby efficiently improve the chemical stability and the photoluminescence quantum yield (PL QY) of the QDs. It is inferred that a shell-like complex structure CdTe(x)(dBSA)(1-x) will form on the surface of the CdTe "core", resulting in the enhancement of PL intensity and the blue shift of the PL peak. This study of the effects of pH and dBSA concentration on optical properties of dBSA-coated QDs suggests that, at pH 6-9, the solution of dBSA-coated CdTe QDs can keep substantial stability and fluorescent brightness, whereas further increase of pH value leads to a dramatic decrease in PL QY and chemical stability. On the other hand, too high or too low initial dBSA concentration in the QD solution results in a decrease of PL QY for dBSA-coated CdTe QDs. This study provides a new approach of preparing stable water-soluble QDs with high PL QY and controllable luminescent colors for biological labeling applications.  相似文献   

15.
A modified method to prepare high-quality thiol-capped CdTe nanocrystals (NCs) was reported in this paper. The experimental results showed that the different molar ratios of the ligands (thioglycolic acid) to monomers (Cd2+ ions) in the precursor solution played an important role in the photoluminescence (PL) quantum yield (QY) of the as-prepared CdTe NCs. When [ligand]/[monomer] = 1.2, the maximum fluorescent emission peak appeared in the orange-red window, and the PL QY increased up to 50% at room temperature without any postpreparative treatment. In the meantime, suitable reaction conditions were in favor of the optimization of the surface structure of NCs, resulting in the relatively high PL QY from green to red. In addition, some differences between hydrothermal synthesis and traditional aqueous synthesis of CdTe NCs were discussed.  相似文献   

16.
硫脲修饰法制备高发光性能CdTe量子点   总被引:1,自引:0,他引:1  
通过巯基水解制备了具有优异荧光特性的碲化镉量子点. 详细研究前驱体镉离子与巯基丙酸(MPA)摩尔比、镉离子浓度等制备条件对大尺寸、高量子产率的亲水性碲化镉量子点光学性能的影响. 在不同的水热生长时间下, 可制备出荧光发射峰位于485-660 nm范围内的不同尺寸的碲化镉水溶性量子点, 荧光发射峰半高宽控制在40-75 nm之间, 量子点的最高量子产率(QY)达到了45%. 并利用硫脲缓慢水解和光解释放自由硫离子, 修饰碲化镉表面, 检测修饰后的量子点在12天内光学性能的变化情况. 通过考察硫脲用量对量子点修饰效果, 发现当n(CdTe)/n(thiourea)=1:4(量子点浓度以镉离子浓度计)时, 硫脲对发射峰为505 nm的碲化镉量子点修饰效果最为理想, 量子点荧光强度加强了5倍, 量子产率达到68.3%.  相似文献   

17.
Highly luminescent water-soluble CdTe quantum dots(QDs) have been synthesized with an electrogenerated precursor.The obtained CdTe QDs can possess good crystallizability,high quantum yield(QY) and favorable stability.Furthermore,a detection system is designed firstly for the investigation of the temperature-dependent PL of the QDs.  相似文献   

18.
水相中CdTe纳米晶的制备及其光学性质   总被引:1,自引:0,他引:1  
用不同稳定剂(巯基乙酸(TGA)、巯基丙酸(MPA)、L-半胱氨酸(L-Cys)、3-巯基-1,2-丙二醇(TG))在水相中制备了CdTe纳米晶, 并用透射电子显微镜(TEM)、X射线光电子能谱(XPS)和X射线粉末衍射(XRD)等技术对其进行了表征. 研究了不同水相合成条件对CdTe纳米晶光学性质的影响, 结果表明, n(Cd):n(Te)、溶液pH值、回流时间以及稳定剂的性质, 对纳米晶的光学性质具有显著影响. 制得的CdTe纳米晶发射峰窄且对称(半高全宽达38 nm), 用不同稳定剂制备的纳米晶发光量子效率有所不同, 用不同的激发波长对纳米晶进行激发时, 发射峰并未表现出明显的移动.  相似文献   

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