Highly luminescent CdSe/ZnSe core-shell quantum dots of one-pot preparation in octadecene

CdSe/ZnSe core-shell quantum dots were synthesized using a new one-pot procedure where the core was prepared in octadecene. A ZnSe shell around a CdSe nanoparticle was formed by the reaction of selenium-richness on the surfaces of CdSe nanoparticles with Zn2+ from the injected zinc stearate precursor. The optical properties, luminescence kinetics, and the effect of shell thickness of as-prepared QDs were studied, which verifies the high quality of the resulting QDs. The new approach is effective not only for preparing core/shell QDs, but also for reducing the complexity of synthesis, toxicity, and reagent cost.     

Rare-earth ion-doped perovskite quantum dots: synthesis and optoelectronic properties

Journal of Materials Science: Materials in Electronics - Rare-earth Nd3+ ions were doped into CsPbBr3 perovskite quantum dots (QDs) by solution-processed method at room temperature. By controlling...     

Highly bright and low turn-on voltage CsPbBr3 quantum dot LEDs via conjugation molecular ligand exchange

Nano Research - All-inorganic CsPbBr3 perovskite quantum dots (QDs) hold great promise as candidate materials for next-generation electroluminescent displays owing to their excellent optoelectronic...     

荧光量子点复合微球的制备

荧光量子点与微球复合起来,可在生物标记,检测筛选等领域发挥重要作用.本文对近年来出现的制备荧光量子点复合微球的方法进行了介绍.     

Highly luminescent metal-organic frameworks through quantum dot doping

The incorporation of highly luminescent core-shell quantum dots (QDs) within a metal-organic framework (MOF) is achieved through a one-pot method. Through appropriate surface functionalization, the QDs are solubilized within MOF-5 growth media. This permits the incorporation of the QDs within the evolving framework during the reaction. The resulting QD@MOF-5 composites are characterized using X-ray fluorescence, cross-sectional confocal microscopy, energy-dispersive X-ray spectroscopy, scanning electron microscopy, and small-angle X-ray scattering. The synergistic combination of luminescent QDs and the controlled porosity of MOF-5 in the QD@MOF-5 composites is harnessed within a prototype molecular sensor that can discriminate on the basis of molecular size.     

Highly luminescent and quantum-yielding CdSe/ZnS core/shell quantum dots synthesized by a kinetically controlled succession route in 18DMA

Highly luminescent and quantum-yielding (QY) CdSe/ZnS core/shell quantum dots (CS QDs) were synthesised via a new succession route in a non-toxic solvent, N,N-Dimethyl-octadecyl-tertiary-amine(18DMA) at a mild temperature. The CS QDs were also proven to be as efficient in reaching high quantum yields (up to 74%) as their reported high-temperature synthesis with organic phosphine ligands. It was demonstrated that the synthesis temperatures directly determine the size by controlling the rate of the monomer diffusion and adsorption. It was also found that the amount of surfactant oleic acid determined the QY of the QDs, whereas it had little influence on the crystallisation.     

Hybrid white-light emitting-LED based on luminescent polyfluorene polymer and quantum dots

We report the fabrication and electroluminescence (EL) characterization of a white-emitting hybrid organic/inorganic light emitting device (LED) by integrating core-shell CdSe/ZnS quantum dots (QDs) acting as a yellow emitter and polyfluorenes as the blue emitter in a multilayered structure. The hybrid white-emitting device was fabricated by spin-coating QDs in varied concentrations onto the layer of polyfluorenes with different functional groups (i.e., sulfur-containing PF1 and PFO). Depending on the QDs concentrations and the design of the hybrid LED, our device is able to exhibit either electroluminescence from QDs or a combination of both PF and QD. The EL spectra at different driving voltages, I-V characteristics, and EL chromaticity of the LEDs based on PF1/QD and PFO/QD LEDs have been measured, investigated, and compared, respectively.     

Dithiocarbamates as capping ligands for water-soluble quantum dots

We investigated the suitability of dithiocarbamate (DTC) species as capping ligands for colloidal CdSe-ZnS quantum dots (QDs). DTC ligands are generated by reacting carbon disulfide (CS(2)) with primary or secondary amines on appropriate precursor molecules. A biphasic exchange procedure efficiently replaces the existing hydrophobic capping ligands on the QD surface with the newly formed DTCs. The reaction conversion is conveniently monitored by UV-vis absorption spectroscopy. Due to their inherent water solubility and variety of side chain functional groups, we used several amino acids as precursors in this reaction/exchange procedure. The performance of DTC-ligands, as evaluated by the preservation of luminescence and colloidal stability, varied widely among amino precursors. For the best DTC-ligand and QD combinations, the quantum yield of the water-soluble QDs rivaled that of the original hydrophobic-capped QDs dispersed in organic solvents. The mean density of DTC-ligands per nanocrystal was estimated through a mass balance calculation which suggested nearly complete coverage of the available nanocrystal surface. The accessibility of the QD surface was evaluated by self-assembly of His-tagged dye-labeled proteins and peptides using fluorescence resonance energy transfer. DTC-capped QDs were also exposed to cell cultures to evaluate their stability and potential use for biological applications. In general, DTC-capped CdSe-ZnS QDs have many advantages over other water-soluble QD formulations and provide a flexible chemistry for controlling the QD surface functionalization. Despite previous literature reports of DTC-stabilized nanocrystals, this study is the first formal investigation of a biphasic exchange method for generating biocompatible core-shell QDs.     

One-pot encapsulation of luminescent quantum dots synthesized in aqueous solution by amphiphilic polymers

A simple one-pot polymer encapsulation method is developed for group II-VI semiconductor quantum dots (QDs) synthesized in aqueous solution. The micelles of amphiphilic polymers, such as octadecylamine-modified poly(acrylic acid), capture and encapsulate the QDs when the original hydrophilic ligands, namely 3-mercaptopropionic acid (MPA), capped on the CdTe/CdS core/shell QDs are partially or fully exchanged by the hydrophobic ligands, 1-dodecanethiol. The molar ratio of the amphiphilic polymer to QDs plays a crucial role in determining the final morphology of the encapsulated structures, including the number of QDs encapsulated in one polymeric micelle. Importantly, the polymer coating significantly improves the optical properties of the QDs, which enhances the photoluminescence quantum yield by about 50%. Furthermore, the photostability of the amphiphilic polymer-coated QDs is much better than that of the synthesized QDs capped with MPA.     

Solution processed high performance perovskite quantum dots/ZnO phototransistors

Phototransistors that can detect visible light have been fabricated using solution processed zinc oxide channel/zirconium oxide gate insulator thin film transis...     

Applications of quantum dots in optical fiber luminescent oxygen sensors

The potential applications of luminescent semiconductor nanocrystals to optical oxygen sensing are explored. The suitability of quantum dots to provide a reference signal in luminescence-based chemical sensors is addressed. A CdSe-ZnS nanocrystal, with an emission peak at 520 nm, is used to provide a reference signal. Measurements of oxygen concentration, which are based on the dynamic quenching of the luminescence of a ruthenium complex, are performed. Both the dye and the nanocrystal are immobilized in a solgel matrix and are excited by a blue LED. Experimental results show that the ratio between the reference and the sensor signals is highly insensitive to fluctuations of the excitation optical power. The use of CdTe, near-infrared quantum dots with an emission wavelength of 680 nm, in combination with a ruthenium complex to provide a new mechanism for oxygen sensing, is investigated. The possibility of creating oxygen sensitivity in different spectral regions is demonstrated. The results obtained clearly show that this technique can be applied to develop a wavelength division multiplexed system of oxygen sensors.     

Calixarene capped quantum dots as luminescent probes for Hg ions

Luminescent and stable CdSe/ZnS core/shell quantum dots (QDs) capped with sulfur calixarene are prepared for the selective determination of mercury ions in acetonitrile with high sensitivity.     

Tuning optical properties of CsPbBr3 perovskite nanocrystals through silver doping

Journal of Materials Science: Materials in Electronics - All-inorganic perovskite nanocrystals have emerged as an alternative for hybrid organic–inorganic perovskite for optoelectronic...     

Mono-disperse silver quantum dots modified formvar film

Formvar films were treated with different doses of silver ions implantation. The implanted silver ions were found to form silver quantum dots (AgQDs) uniformly distributed in the formvar films. While density of the AgQDs increases as the implantation dose increases, their sizes are not sensitive to the dose. It was found that the formvar films implanted with AgQDs have excellent bacteria killing capability. The same implantation approach can also be extended for application in other matrices. As an example, ZnS nanoribbon was implanted with the same approach to obtain uniformly distributed AgQDs with monodispersed size.     

Highly luminescent blue emitting CdS/ZnS core/shell quantum dots via a single-molecular precursor for shell growth

Highly luminescent blue-emitting CdS/ZnS core/shell quantum dots (QDs) were synthesized in N-oleoylmorpholine by two facile steps: first, the CdS core QDs were prepared via a simple one-pot method involving a direct reaction of Cd precursor cadmium stearate and S precursor S powder in solvent N-oleoylmorpholine; second, ZnS shells were successively overcoated on CdS core through the decomposition of single molecular precursor zinc diethyldithiocarbamate. The thickness of shell was precisely tuned by controlling drip feed speed and amount of shell precursor. The obtained CdS/ZnS core/shell QDs showed the maximum photoluminescent quantum yield of 54.8% and narrow spectra bandwidth, exhibiting high monodispersity, good color purity and long fluorescent lifetimes. The CdS/ZnS core/shell QDs with tunable emission wavelength of 424–470 nm were obtained by controlling the thickness of ZnS shell overgrown on different-sized CdS QDs, which are promising materials for blue light-emitting devices.