Stendermathews9885

The optical properties of plasmonic nanocomposites can be manipulated by the adjustment of the intrinsic property of the nanocrystal and/or coupling effect between adjacent nanocrystals from the same layer (intralayer) and/or the neighboring layer (interlayer). Taking advantage of this novel LbL fabrication technique, the properties of multilayer plasmonic nanocrystal arrays stacked in a homogeneous matrix can be manipulated via tuning the interlayer or intralayer coupling between nanocrystals, which can be achieved by sophisticated control of the packing density of two-dimensional nanocrystal arrays in each individual layer or the thickness of the polymer thin film between two adjacent nanocrystal arrays, respectively. These results provide a facile and effective way of designing a more complex multilayer nanostructure with controllable properties in a homogeneous polymer matrix.An emulsion-templated porous material can be formed by polymerizing the continuous phase of high internal phase Pickering emulsions (HIPEs). Although polymerization is a key step to maintain the pore size and integrity of the final sponge, it lowers the effective specific surface area of the final sponge as the continuous phase makes up at least half of the HIPE's volume. Hence, eliminating the need of polymerization not only eases the material processing but also leads to a greater specific surface area. Here, we report a novel strategy in which none of the emulsion phases require polymerization and is therefore a versatile methodology. For this purpose, several oil-in-water Pickering emulsions were prepared using graphene oxide (GO) and cellulose nanocrystals (CNCs) as the stabilizing agents. GO nanosheets are then reduced by mixing the emulsions with an adequate amount of vitamin C as a green reducing agent. Removal of the oil phase via multiple washing and boiling steps results in the formation of the ultimate reduced graphene oxide (rGO)/CNC sponge. The integrity of the structure remains intact and results in the formation of pores that are comparable in size to the droplets because of (i) the strong adhesion of GO and CNC at the oil/water interface in the initial Pickering emulsions and (ii) the strong intermolecular interactions between GO and CNC particles within the water phase. The sponge was then evaluated for its contaminant removal applicability using methylene blue and found to be effective in different water chemistries and outperform previously reported poly(HIPEs) and granular activated carbon. This is the first report on the formation of a polymer-free emulsion-templated sponge, and we believe that this novel nanomaterial paves the road for the fabrication of other emulsion-templated sponges. Although the proposed application in this work is contaminant removal, it could also be utilized in forming electronic devices and sensors because of the incorporation of rGO as a conductive component.Flexible and ultrasensitive biosensing platforms capable of detecting a large number of trinucleotide repeats (TNRs) are crucial for future technology development needed to combat a variety of genetic disorders. For example, trinucleotide CGG repeat expansions in the FMR1 gene can cause Fragile X syndrome (FXS) and Fragile X-associated tremor/ataxia syndrome (FXTAS). Current state-of-the-art technologies to detect repeat sequences are expensive, while relying on complicated procedures, and prone to false negatives. We reasoned that two-dimensional (2D) molybdenum sulfide (MoS2) surfaces may be useful for label-free electrochemical detection of CGG repeats due to its high affinity for guanine bases. Here, we developed a low-cost and sensitive wax-on-plastic electrochemical sensor using 2D MoS2 ink for the detection of CGG repeats. The ink containing few-layered MoS2 nanosheets was prepared and characterized using optical, electrical, electrochemical, and electron microscopic methods. The devices were characterized by electron microscopic and electrochemical methods. Repetitive CGG DNA was adsorbed on a MoS2 surface in a high cationic strength environment and the electrocatalytic current of the CGG/MoS2 interface was recorded using a soluble Fe(CN)6-3/-4 redox probe by differential pulse voltammetry (DPV). The dynamic range for the detection of prehybridized duplexes ranged from 1 aM to 100 nM with a 3.0 aM limit of detection. A detection range of 100 fM to 1 nM was recorded for surface hybridization events. Using this method, we were able to observe selectivity of MoS2 for CGG repeats and distinguish nonpathogenic from disease-associated repeat lengths. The detection of CGG repeat sequences on inkjet printable 2D MoS2 surfaces is a forward step toward developing chip-based rapid and label-free sensors for the detection of repeat expansion sequences.A new hole-transporting material, poly-2-(9H-carbazol-9-yl)-5-(4-vinylphenyl)-5H-benzo[b]carbazole (PBCZCZ), was developed for perovskite light-emitting diodes (PeLEDs). This polymer, which is based on the benzocarbazole moiety, has good solubility in common solvents and enabled the fabrication of highly efficient multilayer perovskite devices. It has excellent film morphology and a high hole mobility of 3.67 × 10-5 cm2 V-1 s-1, which made it possible to vary the device configuration. HDAC inhibitor Green and sky-blue perovskite PeLEDs using PBCZCZ as the hole-transporting layer had current efficiencies and external quantum efficiencies (EQEs) of 43.90 cd A-1 and 8.67% for the green device and 9.07 cd A-1 and 4.04% for the sky-blue device, respectively. The EQE of the green PeLEDs was about 2.5 times higher and that of the sky-blue PeLEDs was about 3 times higher than the device made with the commercial HTL of poly(9-vinylcarbazole) (PVK). The operational device lifetimes of the green and sky-blue PeLEDs made with PBCZCZ were about 4.1 and 4.8 times higher than the PVK-containing device, respectively.It is highly desired to develop new antibacterial agents with superior bactericidal efficiency for minimizing the damage to biological cells. We developed a combined antibacterial nanohybrid exhibiting a superb bactericidal effect and excellent biocompatibility by integrating upconversion nanoparticles (UCNPs) with silver nanoclusters (AgNCs). UCNPs and methylene blue (MB) molecules were encapsulated with silica microspheres via microemulsion, with MB as the photosensitizer. Silver ions (Ag+) were reduced by amino groups on the surface of silica spheres, wherein silver nanoclusters (AgNCs) were formed in situ to produce the nanohybrid, UCNPs@SiO2(MB)@AgNCs. UCNPs emit visible light at 655 nm under excitation by near-infrared radiation (NIR, 980 nm). MB absorbs the emission from UCNPs to generate toxic singlet oxygen (1O2), which leads to the apoptosis of bacteria cells. Meanwhile, silver ions released from AgNCs destroy the bacteria membrane structure. Upon NIR irradiation at 980 nm for 10 min, 8.33 μg mL-1 nanohybrid results in a 100% killing rate for both Gram-positive S.