Temperature‐dependent optical studies of semiconductor quantum dots (QDs) are fundamentally important for a variety of sensing and imaging applications. The steady‐state and time‐resolved photoluminescence properties of CdTe QDs in the size range from 2.3 to 3.1 nm embedded into a protective matrix of NaCl are studied as a function of temperature from 80 to 360 K. The temperature coefficient is found to be strongly dependent on QD size, with the highest sensitivity obtained for the smallest size of QDs. The emission from solid‐state CdTe QD‐based powders is maintained with high color purity over a wide range of temperatures. Photoluminescence lifetime data suggest that temperature dependence of the intrinsic radiative lifetime in CdTe QDs is rather weak, and it is mostly the temperature‐dependent nonradiative decay of CdTe QDs which is responsible for the thermal quenching of photoluminescence intensity. By virtue of the temperature‐dependent photoluminescence behavior, high color purity, photostability, and high photoluminescence quantum yield (26%–37% in the solid state), CdTe QDs embedded in NaCl matrices are useful solid‐state probes for thermal imaging and sensing over a wide range of temperatures within a number of detection schemes and outstanding sensitivity, such as luminescence thermochromic imaging, ratiometric luminescence, and luminescence lifetime thermal sensing. 相似文献
Surfactants represent not only commonly used wetting agents but also substances that can be used as growth modifiers in the process of solid nanoparticle (NP) preparation. In this study we report influential character of different types of surfactants – i.e. ionic (SDS, CTAC) and non-ionic (Tween 80) – on fundamental characteristics of silver NPs, which were prepared by a modified Tollens process. The influential character of surfactants was evaluated throughout a reasonable improvement of the polydispersity (in the case of the tested non-ionic surfactants from 8.5% even down to 2.5%) and in the case of ionic surfactant, SDS and CTAC, also significant change of zeta potential (from −20 to −50 mV for the highest tested concentration of SDS). A slight influence of the tested surfactants was observed on the sizes of the prepared silver NPs. Therefore the obtained results from the performed surfactant-assisted syntheses revealed a possibility how to tailor silver NPs by means of their polydispersity and zeta potential according to the application demands. 相似文献
We have developed a metal‐free process for the aerobic photooxygenation of sulfides to sulfoxides mediated by riboflavin tetraacetate or riboflavin (vitamin B2) photocatalysts and visible light (450 nm) in an acetonitrile‐water (85:15 v/v) mixture. The optimised solvent system leads to both singlet‐oxygen and electron‐transfer pathways in photooxygenation, thus allowing oxidation of electron‐poor and electron‐rich thioanisoles, dialkyl sulfides and sterically hindered sulfides. Besides having a broad substrate scope, the method has very short reaction times and requires low catalyst loading (down to 0.1 mol%). These properties are due to the high photocatalyst stability and the extremely high quantum yields (1.3 for thioanisole oxygenation). Moreover, the method is chemoselective, producing only sulfoxides without overoxidation to sulfones. Taking into account the broad substrate scope, high selectivity and high efficiency, this method distinguishes itself from those previously reported. Other advantages include easy work‐up of the reaction mixture, the availability and biodegradability of the photocatalysts and mild reaction conditions. We demonstrated, on a preparative scale, its practical application in the synthesis of the psychostimulant modafinil, in the selective oxidation of methionine derivatives, and in the detoxification of mustard gas.
A recently developed multi‐functional phosphotriazine‐based polymer is used as a matrix for embedding γ‐Fe2O3 nanoparticles as well as a suitable chemical template for surface modification with silver nanoparticles. For the primary magnetic modification, maghemite nanoparticles are surface modified with oleic acid in order to render them organophilic and to prevent the aggregation of the nanoparticles. This aggregation could occur as the polymer synthesis, based on reaction of phosphonitrilic chlorine and 1,4‐phenylenediamine, takes place in toluene. The surface active amine units of the polymer structure enable the reduction of silver cations to silver nanoparticles, which are well attached and finely dispersed on its surface. The developed nanocomposite represents one of the few magnetically controllable antibacterial agents based on silver nanoparticles. Magnetic measurements reveal the completely suppressed interactions among maghemite nanoparticles because of their perfect surface coating with an organic surfactant and fine dispersion inside the polymer matrix. This magnetic nanocomposite exhibits a high antibacterial and antifungal activity as proven by tests with nine bacterial strains and four candida (yeast genus) species. For the majority of the tested species, the minimum‐inhibition concentrations are below 100 mg L?1, which is comparable to their equivalent minimum‐inhibition concentrations in colloidal silver systems. 相似文献
The synthesis of silver nanoparticles attached on the surface of a hollow cornet‐like polymer matrix which served as a reductant and host matrix is described. This hybrid organic/inorganic macromolecular matrix is exhibiting anion‐exchange properties, porous structure and hollow morphologies, and absorptions in the visible light region. Due to the anion‐exchange property and the 3D orientation of the macromolecular chains the material is defining a new functional organic/inorganic hybrid. For the synthesis of nanoparticles, no other reducing agents were used and silver nanoparticles with a mean diameter of less than 20 nm were attached on the surface of the polymer, thus inheriting the composite with high antibacterial activity tested in bacterial strains and yeasts.
The paper presents a family of distributed file structures, coined DiFS, for record structured, disk resident files with key based exact or interval match access. The file is organized into buckets that are spread among multiple servers, where a server may hold several buckets. Client requests are serviced by mapping keys onto buckets and looking up the corresponding server in an address table. Dynamic growth, in terms of file size and access load, is supported by bucket splits and bucket migrations onto the existing or newly created servers.The major problem that we are addressing is achieving scalability in the sense that both the file size and the client throughput can be scaled up by linearly increasing the number of servers and dynamically redistributing the data. Unlike previous work with similar objectives, our data redistribution considers explicitly the cost/performance ratio of the system by aiming to minimize the number of servers that are used to provide the required performance. A new server is added only if the overall server load in the system does not drop below a pre-specified threshold. Simulation results demonstrate the scalability with controlled cost/performance and the importance of global load control. The impact of various tuning parameters on the effectiveness of the load control is studied in detail. Finally, we compare our approach with other approaches known to date and demonstrate that each of the previous approaches can be recast as a special case of our model.
Recommended by: Mei HsuThis material is based in part upon work supported by a grant from Hewlett-Packard Corporation and by NSF under grant IRI-9221947. 相似文献