共查询到20条相似文献,搜索用时 31 毫秒
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CdS纳米晶与多肽分子相互作用研究 总被引:2,自引:0,他引:2
研究了半导体CdS纳米晶的表面功能化及荧光光谱特性, 并利用静电/配位自组装方法实现了多肽和CdS纳米晶的生物无机偶联, 研究了纳米晶多肽偶联体系的荧光光谱以及多肽与CdS纳米晶之间的相互作用. 结果表明: 含巯基多肽对CdS纳米晶表面形成完善包覆, 消除CdS纳米晶表面缺陷, 使CdS纳米晶荧光增强; 含端氨基多肽使CdS纳米晶荧光出现先升后降趋势; 其余不含巯基和氨基的多肽均猝灭CdS纳米晶荧光, 猝灭机制属于形成化合物所引起的静态猝灭, 它们的结合常数约为2×104, 结合位点数约为0.87~1.00. 相似文献
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YUE Yang GE Mei-ying LIU Yan WU Jie CHEN Ping LIN Lie LIU Yu-feng SUN Yan CHEN Xin DAI Ning 《高等学校化学研究》2010,26(6):871-875
We described a facile method for preparing CdSe/CdS/ZnS core/shell/shell nanocrystals from air-stable single source precursors.The single source precursors of cadmium ethylxanthate and zinc ethylxanthate were used to form CdS and ZnS shell layers in octadecene.An efficient modification of CdSe/CdS/ZnS nanocrystals was subsequently performed to obtain hydrophilic nanocrystal fluorophores with good stability in a pH range of 1.6-10. 相似文献
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Here we report the formation and spectroscopic properties of cadmium sulfide (CdS) nanocrystal systems: individual nanocrystal and CdS aggregates. The optical absorption and luminescence spectra of the aggregated CdS nanocrystals and individual nanocrystal show exciton aggregate and individual exciton characteristics. Although it is not Bose-Einstein condensation, such aggregated quantum dots (QDs) seem to supply us opportunity to study the interactions and condensation of excitons in multi-QDs system, not in the separated QDs system. 相似文献
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Dai Q Li D Chen H Kan S Li H Gao S Hou Y Liu B Zou G 《The journal of physical chemistry. B》2006,110(33):16508-16513
The addition of a secondary ligand, trioctylphosphine oxide, in the synthesis of cadmium selenide nanocrystals performed in a system with oleic acid as the primary ligand and octadecene as the noncoordinating solvent gives rise to the improvement of nanocrystal size distribution. This phenomenon, which is more significant in the nucleation process than in the growth process, demonstrates that the existence of trioctylphosphine oxide allows for superior nucleation control and permits the facile and reproducible production of extremely small CdSe nanocrystals with narrow size distribution. A systematic study of the nanocrystal formation processes shows that the well-established colloidal nanocrystal growth mechanism, in which nucleation is followed by focusing of size distribution and ended with defocusing of size distribution, cannot be applied to our reactions. Instead, we observed an exceptional type of growth mechanism in which, after nucleation, clear defocusing instead of focusing follows; then slight focusing occurs. 相似文献
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Shevchenko EV Talapin DV Schnablegger H Kornowski A Festin O Svedlindh P Haase M Weller H 《Journal of the American Chemical Society》2003,125(30):9090-9101
High quality CoPt(3) nanocrystals were synthesized via simultaneous reduction of platinum acetylacetonate and thermodecomposition of cobalt carbonyl in the presence of 1-adamantanecarboxylic acid and hexadecylamine as stabilizing agents. The high flexibility and reproducibility of the synthesis allows us to consider CoPt(3) nanocrystals as a model system for the hot organometallic synthesis of metal nanoparticles. Different experimental conditions (reaction temperature, concentration of stabilizing agents, ratio between cobalt and platinum precursors, etc.) have been investigated to reveal the processes governing the formation of the metal alloy nanocrystals. It was found that CoPt(3) nanocrystals nucleate and grow up to their final size at an early stage of the synthesis with no Ostwald ripening observed upon further heating. In this case, the nanocrystal size can be controlled only via proper balance between the rates for nucleation and for growth from the molecular precursors. Thus, the size of CoPt(3) nanocrystals can be precisely tuned from approximately 3 nm up to approximately 18 nm in a predictable and reproducible way. The mechanism of homogeneous nucleation, evolution of the nanocrystal ensemble in the absence of Ostwald ripening, nanocrystal faceting, and size-dependent magnetic properties are investigated and discussed on the example of CoPt(3) magnetic alloy nanocrystals. The developed approach was found to be applicable to other systems, e.g., FePt and CoPd(2) magnetic alloy nanocrystals. 相似文献
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Wang Q Pan D Jiang S Ji X An L Jiang B 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,11(13):3843-3848
A new two-phase route has been developed to synthesize high-quality CdS nanocrystals with a narrow size distribution and a high photoluminescence (PL) quantum yield (QY). In the two-phase system, toluene and water were used as separate solvents for cadmium myristate (CdM2) and thiourea, which served as cadmium source and sulfur source, respectively, and oleic acid (OA) was used as a ligand for stabilizing the nanocrystals. The reactions were completed in the heated autoclaves. The initial Cd/S molar ratio of the precursors and the reaction temperature were found to be factors that affected the growth of nanocrystals. Furthermore, a seeding-growth technique was developed to synthesize CdS nanocrystals of different sizes, which exhibit PL peaks with quite similar full width at half-maximum (FWHM) values compared to those of the initial nanocrystal seeds in all cases. 相似文献
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Synthesis of hybrid CdS-Au colloidal nanostructures 总被引:1,自引:0,他引:1
We explore the growth mechanism of gold nanocrystals onto preformed cadmium sulfide nanorods to form hybrid metal nanocrystal/semiconductor nanorod colloids. By manipulating the growth conditions, it is possible to obtain nanostructures exhibiting Au nanocrystal growth at only one nanorod tip, at both tips, or at multiple locations along the nanorod surface. Under anaerobic conditions, Au growth occurs only at one tip of the nanorods, producing asymmetric structures. In contrast, the presence of oxygen and trace amounts of water during the reaction promotes etching of the nanorod surface, providing additional sites for metal deposition. Three growth stages are observed when Au growth is performed under air: (1) Au nanocrystal formation at both nanorod tips, (2) growth onto defect sites on the nanorod surface, and finally (3) a ripening process in which one nanocrystal tip grows at the expense of the other particles present on the nanorod. Analysis of the hybrid nanostructures by high-resolution TEM shows that there is no preferred orientation between the Au nanocrystal and the CdS nanorod, indicating that growth is nonepitaxial. The optical signatures of the nanocrystals and the nanorods (i.e., the surface plasmon and first exciton transition peaks, respectively) are spectrally distinct, allowing the different stages of the growth process to be easily monitored. The initial CdS nanorods exhibit band gap and trap state emission, both of which are quenched during Au growth. 相似文献
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Huang F Chen G 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2008,70(2):318-323
The water-soluble L-cysteine-modified CdSe/CdS core/shell nanocrystals (expressed as CdSe/CdS/Cys nanocrystals) have been synthesized in aqueous by using L-cysteine as stabilizer. The size, shape, component and spectral property of CdSe/CdS/Cys nanocrystals were characterized by high-resolution transmission electron microscope (HRTEM), energy dispersive X-ray fluorescence (EDX), infrared spectrum (IR) and photoluminescence (PL). The results showed that the spherical CdSe/CdS/Cys nanocrystals with an average diameter of 2.3 nm have favorable fluorescent property, theirs photostability and fluorescence intensity are enhanced greatly after overcoating with CdS. The cysteine modified on the surface of core/shell CdSe/CdS nanocrystals renders the nanocrystals water-soluble and biocompatible. Based on the fluorescence quenching of the nanocrystals in the presence of calf thymus deoxyribonucleic acid (ct-DNA), a fluorescence quenching method has been developed for the determination of ct-DNA by using the nanocrystals as a novel fluorescence probe. The pH value of the system was selected at pH 7.4, with excitation and emission wavelength at 380 and 522 nm, respectively. Under the optimal conditions, the fluorescence quenching intensity of the system is linear with the concentration of ct-DNA in the range of 0.1-3.5 microg/mL (r=0.9987). The detection limit is 0.06 microg/mL. And two synthetic samples were analyzed satisfactorily. 相似文献
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Inorganic cluster syntheses of TM2+-doped quantum dots (CdSe, CdS, CdSe/CdS): physical property dependence on dopant locale 总被引:1,自引:0,他引:1
A series of colloidal transition-metal-doped chalcogenide semiconductor nanocrystals (TM2+:CdSe, TM2+:CdS, etc.) has been prepared by thermal decomposition of inorganic cluster precursors. It is shown through extensive spectroscopic and structural characterization that the nanocrystals prepared following literature procedures for synthesis of TM2+:CdSe nanocrystals actually possess an unintended CdSe/TM2+:CdS core/shell morphology. The conditions required for successful formation of TM2+:CdSe and TM2+:CdS by cluster decomposition have been determined. Magneto-optical and photoluminescence spectroscopic results for this series of doped nanocrystals reveal major physical consequences of dopant localization within the shell and demonstrate the capacity to engineer dopant-carrier exchange interactions via core/shell doping strategies. The results presented here illustrate some of the remarkable and unexpected complexities that can arise in nanocrystal doping chemistries and emphasize the need for meticulous characterization to avoid false positives. 相似文献
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Younan Xia Prof. Yujie Xiong Dr. Byungkwon Lim Dr. Sara E. Skrabalak Dr. 《Angewandte Chemie (International ed. in English)》2009,48(1):60-103
Nanocrystals are fundamental to modern science and technology. Mastery over the shape of a nanocrystal enables control of its properties and enhancement of its usefulness for a given application. Our aim is to present a comprehensive review of current research activities that center on the shape‐controlled synthesis of metal nanocrystals. We begin with a brief introduction to nucleation and growth within the context of metal nanocrystal synthesis, followed by a discussion of the possible shapes that a metal nanocrystal might take under different conditions. We then focus on a variety of experimental parameters that have been explored to manipulate the nucleation and growth of metal nanocrystals in solution‐phase syntheses in an effort to generate specific shapes. We then elaborate on these approaches by selecting examples in which there is already reasonable understanding for the observed shape control or at least the protocols have proven to be reproducible and controllable. Finally, we highlight a number of applications that have been enabled and/or enhanced by the shape‐controlled synthesis of metal nanocrystals. We conclude this article with personal perspectives on the directions toward which future research in this field might take. 相似文献
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Large-scale synthesis of nearly monodisperse CdSe/CdS core/shell nanocrystals using air-stable reagents via successive ion layer adsorption and reaction 总被引:10,自引:0,他引:10
Li JJ Wang YA Guo W Keay JC Mishima TD Johnson MB Peng X 《Journal of the American Chemical Society》2003,125(41):12567-12575
Successive ion layer adsorption and reaction (SILAR) originally developed for the deposition of thin films on solid substrates from solution baths is introduced as a technique for the growth of high-quality core/shell nanocrystals of compound semiconductors. The growth of the shell was designed to grow one monolayer at a time by alternating injections of air-stable and inexpensive cationic and anionic precursors into the reaction mixture with core nanocrystals. The principles of SILAR were demonstrated by the CdSe/CdS core/shell model system using its shell-thickness-dependent optical spectra as the probes with CdO and elemental S as the precursors. For this reaction system, a relatively high temperature, about 220-240 degrees C, was found to be essential for SILAR to fully occur. The synthesis can be readily performed on a multigram scale. The size distribution of the core/shell nanocrystals was maintained even after five monolayers of CdS shell (equivalent to about 10 times volume increase for a 3.5 nm CdSe nanocrystal) were grown onto the core nanocrystals. The epitaxial growth of the core/shell structures was verified by optical spectroscopy, TEM, XRD, and XPS. The photoluminescence quantum yield (PL QY) of the as-prepared CdSe/CdS core/shell nanocrystals ranged from 20% to 40%, and the PL full-width at half-maximum (fwhm) was maintained between 23 and 26 nm, even for those nanocrystals for which the UV-vis and PL peaks red-shifted by about 50 nm from that of the core nanocrystals. Several types of brightening phenomena were observed, some of which can further boost the PL QY of the core/shell nanocrystals. The CdSe/CdS core/shell nanocrystals were found to be superior in comparison to the highly luminescent CdSe plain core nanocrystals. The SILAR technique reported here can also be used for the growth of complex colloidal semiconductor nanostructures, such as quantum shells and colloidal quantum wells. 相似文献
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We reported controllable synthesis of CdS nanocrystal-polymer transparent hybrids by using polymethylmethacrylate (PMMA) as a polymer matrix. In a typical run, the appropriate amounts of cadmium chloride (CdCl2) and sodium sulfide (Na2S) in the presence of 2-mercaptoethanol (ME) as the organic ligand are well dispersed in H2O/DMF solution without any aggregation. From a combination of transmission electron microscopy (TEM) and a computing method of Brus’s model according UV-vis absorption spectra, the particle size of as-prepared hydroxyl-coated CdS nanocrystal was determined to be about 5 nm. Then, with the surface treatment with methacryloxypropyltrimethoxysilane (MPS), CdS-PMMA hybrids were obtained via free radical polymerization in situ. FT-IR characterization indicates the formation of robust bonding between CdS nanocrystals and the organic ligand and the formation of double-bond functional CdS nanocrystals. The TGA measurement displays CdS-PMMA hybrids possess better thermal stability compared with pure PMMA polymer. The fluorescence measurement shows that CdS nanocrystals and CdS-PMMA hybrids exhibit good optical properties. Also, the luminescent photographs taken under ultraviolet light prove the luminescence properties. 相似文献
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Semiconductor nanocrystals are of a great interest for many practical applications which motivates the search of low cost and environmental-friendly methods for their manufacturing. Here we report the synthesis of CdSe and CdS nanoparticles utilizing composite matrix of liquid paraffin as a non-coordinating solvent and stearic acid as a coordinating ligand. The nanoparticle growth kinetics is compared to that of the classical synthesis in trioctylphosphine oxide matrix. It is found that the nucleation and crystal growth are remarkably affected by the coordinating ligand. The CdSe and CdS nanocrystals can be isolated and purified from the matrix which makes it possible their large-scale synthesis for applications. 相似文献
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Swafford LA Weigand LA Bowers MJ McBride JR Rapaport JL Watt TL Dixit SK Feldman LC Rosenthal SJ 《Journal of the American Chemical Society》2006,128(37):12299-12306
Alloy nanocrystals provide an additional degree of freedom in selecting desirable properties for nanoscale engineering because their physical and optical properties depend on both size and composition. We report the pyrolytic synthesis of homogeneously alloyed CdS(x)Se(1-x) nanocrystals in all proportions. The nanocrystals are characterized using UV-visible absorption spectroscopy, transmission electron microscopy, X-ray diffractrometry, and Rutherford backscattering spectrometry to determine precisely structure, size, and composition. The dependence of band gap on nanocrystal size and composition is elucidated, yielding a bowing constant of 0.29, in agreement with bulk values. In addition, the morphology of the resultant nanocrystals can be altered by changing the reaction conditions, generating structures ranging from homogeneous, spherical nanocrystals to one-dimensional gradient nanorods. 相似文献
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Sounart TL Safier PA Voigt JA Hoyt J Tallant DR Matzke CM Michalske TA 《Lab on a chip》2007,7(7):908-915
Microfluidic systems provide a unique platform for investigation of fundamental reaction processes, which is critical to understanding how to control nanostructure synthesis on a production scale. We have examined the synthesis of cysteine-capped CdS quantum dot nanocrystals (CdS-Cys) between two interdiffusing reagent streams in a continuous-flow microfluidic reactor. Using spatially resolved photoluminescence imaging and spectroscopy of the microreactor, we have acquired kinetic and mechanistic data on the CdS-Cys nanoparticle nucleation and growth, and observed a binary shift in the particle emission spectrum from a higher (2.9 eV) to lower (2.5 eV) energy emission peak within the first second of residence time. Several reactor models have been tested against the spatially and spectrally resolved signals, which suggest that homogeneous reaction and particle nucleation are diffusion-limited and occur only at the boundary between the two laminar streams, while a slower activation process occurs on a longer (seconds) time scale. The results provide direct insight into the rapid processes that occur during crystallization in microfluidic mixing channels, and demonstrate the potential of using controlled microfluidic environments with spatially resolved monitoring to conduct fundamental studies of nanocrystal nucleation and growth. 相似文献
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Luminescent CdSe/CdS core/shell nanocrystals in dendron boxes: superior chemical,photochemical and thermal stability 总被引:5,自引:0,他引:5
The surface ligands, generation-3 (G3) dendrons, on each semiconductor nanocrystal were globally cross-linked through ring-closing metathesis (RCM). The global cross-linking of the dendron ligands sealed each nanocrystal in a dendron box, which yielded box-nanocrystals. Although the dendron ligands coated CdSe nanocrystals (CdSe dendron-nanocrystals) were already quite stable, the stability of CdSe box-nanocrystals against chemical, photochemical, and thermal treatments were dramatically improved in comparison to that of the original dendron-nanocrystals. Furthermore, the box structure of the ligands monolayer coupled with the stable inorganic CdSe/CdS core/shell nanocrystals resulted in a class of extremely stable nanocrystal/ligands complexes. The band edge photoluminescence of the core/shell dendron-nanocrystals and box-nanocrystals were partially remained, and could be further brightened through controlled chemical oxidation or photooxidation. Practically, the stability of the box-nanocrystals is sufficient for most fundamental studies and technical applications. The box-nanocrystals may represent a general solution for the commonly encountered instability for many types of colloidal nanocrystals. The size distribution of the empty dendron boxes formed by the dissolution of the inorganic nanocrystals in concentrated HCl was very narrow. The empty boxes as new types of polymer capsules are soluble in solution, mesoporous, and with a very thin but stable peripheral. Those nanometer-sized cavities should be of interest for many purposes in the field of solution host-guest chemistry. 相似文献