Organic–inorganic lead-halide perovskites have been the subject of recent intense interest due to their unusually strong photovoltaic performance. A new addition to the perovskite family is ...all-inorganic Cs–Pb-halide perovskite nanocrystals, or quantum dots, fabricated via a moderate-temperature colloidal synthesis. While being only recently introduced to the research community, these nanomaterials have already shown promise for a range of applications from color-converting phosphors and light-emitting diodes to lasers, and even room-temperature single-photon sources. Knowledge of the optical properties of perovskite quantum dots still remains vastly incomplete. Here we apply various time-resolved spectroscopic techniques to conduct a comprehensive study of spectral and dynamical characteristics of single- and multiexciton states in CsPbX3 nanocrystals with X being either Br, I, or their mixture. Specifically, we measure exciton radiative lifetimes, absorption cross-sections, and derive the degeneracies of the band-edge electron and hole states. We also characterize the rates of intraband cooling and nonradiative Auger recombination and evaluate the strength of exciton–exciton coupling. The overall conclusion of this work is that spectroscopic properties of Cs–Pb-halide quantum dots are largely similar to those of quantum dots of more traditional semiconductors such as CdSe and PbSe. At the same time, we observe some distinctions including, for example, an appreciable effect of the halide identity on radiative lifetimes, considerably shorter biexciton Auger lifetimes, and apparent deviation of their size dependence from the “universal volume scaling” previously observed for many traditional nanocrystal systems. The high efficiency of Auger decay in perovskite quantum dots is detrimental to their prospective applications in light-emitting devices and lasers. This points toward the need for the development of approaches for effective suppression of Auger recombination in these nanomaterials, using perhaps insights gained from previous studies of II–VI nanocrystals.
The low efficiency and fast degradation of devices from ink-jet printing process hinders the application of quantum dot light emitting diodes on next generation displays. Passivating the trap states ...caused by both anion and cation under-coordinated sites on the quantum dot surface with proper ligands for ink-jet printing processing reminds a problem. Here we show, by adapting the idea of dual ionic passivation of quantum dots, ink-jet printed quantum dot light emitting diodes with an external quantum efficiency over 16% and half lifetime of more than 1,721,000 hours were reported for the first time. The liquid phase exchange of ligands fulfills the requirements of ink-jet printing processing for possible mass production. And the performance from ink-jet printed quantum dot light emitting diodes truly opens the gate of quantum dot light emitting diode application for industry.
The brittleness of ethyl cellulose (EC) film limited its full applications, and the addition of plasticizers is one of the most common methods to reduce its brittleness. However, the mechanical ...properties are normally dropped with the addition of plasticizers. Herein, cellulose nanocrystal (CNC) was chosen as a reinforcing agent to improve its mechanical properties. CNC was firstly extracted from the tobacco-stem and then modified by epoxidized soybean oil (ESO) via ring-opening grafting to obtain epoxidized soybean oil grafting CNC (ECNC). The grafting effect was evaluated by FTIR and XPS. After that, the films of ECNC/EC nanocomposites were prepared by the solution-casting method, and their mechanical, thermal and optical properties and fracture morphology were investigated. The results showed that at 4 phr loading of ECNC, the tensile strength of the nanocomposite film was up to 43.7 Mpa (about twice as much as that of the EC film plasticized by ESO), and the elongation at break was not influenced. Moreover, a higher thermal decomposition temperature was achieved for the ECNC/EC films. Besides, owing to the good dispersion, ECNC had no significant impact on the transparency, and the films presented high light transmittance in the visible light region.
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•A bilayer hydrogel was prepared by interfacial reaction in one step.•A synergistic function exists between the two layers of hydrogel.•High strength, toughness and durable water ...retention were achieved.•The bilayer hydrogel shows well antibacterial ability and accelerated healing effect.
The main limit of hydrogel used as an independent wound dressing is its poor water retention, brittleness, and weak skin adhesion. Focusing on it, the macromolecular cross-linked chitosan and polyacrylamide double network hydrogel (C-A) is chosen as a functional layer, another robust poly(vinyl alcohol)-polyacrylamide/glycerin (P-A) protective layer is designed to cover its surface, an interfacial reaction happens to link two layers tightly for achieving the function synergy. In this double-layer hydrogel (DH) dressing, the surface P-A layer with strong water locking ability could keep the wound surface moist for a long time, high strength and toughness make the dressing maintain integrity under large deformation and stress to strengthen wound protection, and the C-A layer with modest adhesion ensures the dressing fit the skin, the synergistic swelling ability could guarantee the fast absorption for the wound exudate. Moreover, in vitro and in vivo tests, the DH dressing exhibits excellent antibacterial and cytocompatibility, it could significantly accelerate skin tissue regeneration and wound closure than the commercial hydrocolloid dressings. In general, this DH dressing is easy to prepare and shows superior comprehensive performance, revealing the great potential for use as an independently applied wound dressing.
We here evaluated the potential anti-colorectal cancer activity by erastin, a voltage-dependent anion channel (VDAC)-binding compound. Our in vitro studies showed that erastin exerted potent ...cytotoxic effects against multiple human colorectal cancer cell lines, possibly via inducing oxidative stress and caspase-9 dependent cell apoptosis. Further, mitochondrial permeability transition pore (mPTP) opening was observed in erastin-treated cancer cells, which was evidenced by VDAC-1 and cyclophilin-D (Cyp-D) association, mitochondrial depolarization, and cytochrome C release. Caspase inhibitors, the ROS scavenger MnTBAP, and mPTP blockers (sanglifehrin A, cyclosporin A and bongkrekic acid), as well as shRNA-mediated knockdown of VDAC-1, all significantly attenuated erastin-induced cytotoxicity and apoptosis in colorectal cancer cells. On the other hand, over-expression of VDAC-1 augmented erastin-induced ROS production, mPTP opening, and colorectal cancer cell apoptosis. In vivo studies showed that intraperitoneal injection of erastin at well-tolerated doses dramatically inhibited HT-29 xenograft growth in severe combined immunodeficient (SCID) mice. Together, these results demonstrate that erastin is cytotoxic and pro-apoptotic to colorectal cancer cells. Erastin may be further investigated as a novel anti-colorectal cancer agent.
We report on the temperature-dependent Hall effect characteristics of nanocrystal (NC) arrays prepared from colloidal InAs NCs capped with metal chalcogenide complex (MCC) ligands (In2Se4 2– and ...Cu7S4 –). Our study demonstrates that Hall effect measurements are a powerful way of exploring the fundamental properties of NC solids. We found that solution-cast 5.3 nm InAs NC films capped with copper sulfide MCC ligands exhibited high Hall mobility values over 16 cm2/(V s). We also showed that the nature of MCC ligands can control doping in NC solids. The comparative study of the temperature-dependent Hall and field-effect mobility values provides valuable insights concerning the charge transport mechanism and points to the transition from a weak to a strong coupling regime in all-inorganic InAs NC solids.
The use of semiconductor nanocrystal quantum dots (QDs) in optoelectronic devices typically requires postsynthetic chemical surface treatments to enhance electronic coupling between QDs and allow for ...efficient charge transport in QD films. Despite their importance in solar cells and infrared (IR) light-emitting diodes and photodetectors, advances in these chemical treatments for lead chalcogenide (PbE; E = S, Se, Te) QDs have lagged behind those of, for instance, II–VI semiconductor QDs. Here, we introduce a method for fast and effective ligand exchange for PbE QDs in solution, resulting in QDs completely passivated by a wide range of small anionic ligands. Due to electrostatic stabilization, these QDs are readily dispersible in polar solvents, in which they form highly concentrated solutions that remain stable for months. QDs of all three Pb chalcogenides retain their photoluminescence, allowing for a detailed study of the effect of the surface ionic double layer on electronic passivation of QD surfaces, which we find can be explained using the hard/soft acid–base theory. Importantly, we prepare highly conductive films of PbS, PbSe, and PbTe QDs by directly casting from solution without further chemical treatment, as determined by field-effect transistor measurements. This method allows for precise control over the surface chemistry, and therefore the transport properties of deposited films. It also permits single-step deposition of films of unprecedented thickness via continuous processing techniques, as we demonstrate by preparing a dense, smooth, 5.3-μm-thick PbSe QD film via doctor-blading. As such, it offers important advantages over laborious layer-by-layer methods for solar cells and photodetectors, while opening the door to new possibilities in ionizing-radiation detectors.
The hydrophobic surface on aluminum alloy fabricated by anodizing and polymeric coating. Display omitted
► Anodizing and polymeric coating were used to prepare a superhydrophobic surface on aluminum ...alloy. ► Superhydrophobic surfaces with a high water contact angle of 162° and a low rolling angle of 2° were obtained. ► The method is facile, and the materials are inexpensive, and is expected to be used widely.
We reported the preparation of the superhydrophobic surface on aluminum alloy via anodizing and polymeric coating. Both the different anodizing processes and different polymeric coatings of aluminum alloy were investigated. The effects of different anodizing conditions, such as electrolyte concentration, anodization time and current on the superhydrophobic surface were discussed. The results showed that a good superhydrophobic surface was facilely fabricated by polypropylene (PP) coating after anodizing. The optimum conditions for anodizing were determined by orthogonal experiments. When the concentration of oxalic acid was 10g/L, the concentration of NaCl was 1.25g/L, anodization time was 40min, and anodization current was 0.4A, the best superhydrophobic surface on aluminum alloy with the contact angle (CA) of 162° and the sliding angle of 2° was obtained. On the other hand, the different polymeric coatings, such as polystyrene (PS), polypropylene (PP) and polypropylene grafting maleic anhydride (PP-g-MAH) were used to coat the aluminum alloy surface after anodizing. The results showed that the superhydrophobicity was most excellent by coating PP, while the duration of the hydrophobic surface was poor. By modifying the surface with the silane coupling agent before PP coating, the duration of the superhydrophobic surface was improved. The morphologies of the superhydrophobic surface were further confirmed by optical microscope (OM) and scanning electron microscope (SEM). Combined with the material of PP with the low surface free energy, the micro/nano-structures of the surface resulted in the superhydrophobicity of the aluminum alloy surface.
During a heating experiment, there are two sources of heat that increase the temperature of a coal sample: the heat released by the oxidation reaction of the coal itself, and the heat provided by the ...experimental system. Here, we propose a method for measuring the thermal effect of oxidation and self-ignition through a reference experiment conducted with a material that is physically similar to coal but does not combust. The reference material used was an aggregate of alumina, fly ash, and concrete, and experiments were conducted on both materials simultaneously. The temperature of the coal sample was obtained under self-heating conditions, and compared with that of the non-combusting material. The relationship of temperature as a function of time for both materials was determined from the data, the comparison of which allowed for the thermal effect of oxidation and coal spontaneous combustion (CSC) to be calculated. The reliability of the thermal effect data obtained by the experiment was verified by chemical bond energy estimation. These results provide theoretical guidance for on-site fire prevention and extinguishing in coal mines, and are important for the further development of the understanding of CSC.
In micro injection molding, the cavity thickness and surface roughness are the main effects factors of polymer flow in the die designing and affect the quality of molded products significantly. In ...this study, the effects of cavity thickness and roughness of cavity surface were investigated mainly on polymer flow during molding and on the roughness of molded products. The parts were molded in the cavities with the thickness from 0.05 mm to 0.25 mm and surface roughness from R
= 46.55 nm to R
= 462.57 nm, respectively. The filling integrities and roughness replication ratio of molded parts were used to evaluate the statements of polymer flow and microstructure replication during micro injection molding, respectively. The results showed that the filling integrity changing trends in the thinner cavities were obviously different or even opposite to those in the thicker cavities with the changing of cavity surface roughness instead of single trend in the conventional studies. For each cavity surface roughness, the filling integrity showed an upward trend with the increasing cavity thickness. In different cavity thickness, the maximum gap of filling integrity was 23.76 mm, reaching 544.94% from 0.05 mm to 0.25 mm. Additionally, the surface roughness ratio was slightly smaller than one before, reaching the polymer surface roughness limit around R
= 71.27 nm, which was decided by the nature of the polymer itself. This study proposed the references for the design and fabrication of mold cavities and parts, and saved time and cost in the actual product manufacturing.
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