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In this study, an AgBr/Ag3PO4 (ABAP) photocatalyst has been prepared via a facile one-pot anion-exchange method. SEM, XRD, XPS and UV-Vis DRS characterization techniques are carried out to study the structural and physicochemical characteristics of the AgBr/Ag3PO4 composites. The ABAP photocatalyst exhibited outstanding photocatalytic capability for the photodegradation of rhodamine B (RhB) under visible light irradiation. The optimal ABAP-48% composite displayed the highest photocatalytic activity; a complete degradation was attained in 25 min under visible light irradiation. The excellent stability and reusability of ABAP catalysts were examined by five subsequent runs. A probable degradation mechanism of ABAP composites was carefully surveyed. Furthermore, radical trapping experiments confirmed that the ˙O2 - radical was the main active species in the photodegradation reaction.Silver cyanamide (Ag2NCN) is a type of functional semiconductor material with a visible-light response. Ag2NCN nanocrystals with nanorod bundle-like (RB) or straw bundle-like (SB) assemblies were successfully prepared, and it was found that the as-prepared Ag2NCN nanorod bundle (RB) samples had a narrower bandgap of 2.16 eV, which was lower than those reported. As a result, RB samples demonstrated a higher photocatalytic activity towards tetracycline (TC) degradation. The analyses of active species confirmed that both the photo-generated holes and ˙O2 - radicals of the RB sample played significant roles during the process of photocatalytic degradation of TC, and the holes were the main active species. These results indicated that effective charge separation could be achieved by adjusting the morphologies of Ag2NCN nanocrystals. This study provides a new approach to prepare Ag2NCN nanocrystals with a narrower bandgap and strong visible-light response towards antibiotic degradation.A potentiometric sensor, based on the glassy carbon electrode (GCE) modified with a magnetic multi-walled carbon nanotubes/cesium ion-imprinted polymer composite (MMWCNTs@Cs-IIP), is introduced for the detection of cesium(i). The IIP was synthesized using cesium ions as the template ions, chitosan as the functional monomer and glutaraldehyde as the cross-linking agent. The membrane, which was coated on the surface of the GCE, was prepared using MMWCNTs@Cs(i)-IIP as the modifier, PVC as the neutral carrier, 2-nitrophenyloctyl ether as the plasticizer and sodium tetraphenylborate as the lipophilic salt. The proposed sensor exhibited a Nernstian slope of 0.05954 V dec-1 in a working concentration range of 1 × 10-7 to 1 × 10-4 M (mol L-1) with a detection limit of 4 × 10-8 M. The sensor exhibited high selectivity for cesium ions and was successfully applied for the determination of Cs(i) in real samples.The dissolution behavior of the precious metals gold, platinum, rhodium and palladium in the trihexyl(tetradecyl)phosphonium trihalide ionic liquids [P66614][Cl3], [P66614][Br3], [P66614][IBr2] and [P66614][I3] was investigated. The highest dissolution rates were observed for the trichloride ionic liquid [P66614][Cl3] and this system was investigated in more detail. The effects of the trichloride concentration in the ionic liquid and temperature were studied, reaching higher leaching rates at higher trichloride conversions and increased temperatures. The stability of the trichloride anion at these elevated temperatures was studied by Raman spectroscopy. It was found that the trichloride anion decomposed during leaching at higher temperatures, showing the requirement to store these reactive compounds in sealed and cool environments, shielded from light. [https://www.selleckchem.com/products/alkbh5-inhibitor-2.html see more] The optimal leaching conditions were applied for the recovery of palladium from ceramic monolith powder, obtained from end-of-life automotive catalysts. The catalyst powder was contacted with the ionic liquid [P66614][Cl3] and the metal concentrations in the ionic liquid were monitored. The trihalide ionic liquid allowed a more selective leaching of palladium compared to other metals present at very high concentrations in the monolith structure, like magnesium. The relative ratio of palladium over magnesium increased by two orders of magnitude compared to the original catalyst composition. The effect of the contact time between the catalyst powder and the ionic liquid on the metal concentrations in the leachate was investigated, but no significant improvement in the selectivity was observed.Various physical structures have improved light-harvesting and power-conversion efficiency in organic photovoltaic devices, and optical simulations have supported the improvement of device characteristics. Herein, we experimentally investigated how microlens arrays manipulate light propagation in microlens films and material stacks for organic photovoltaics to understand the influence of the constituent materials and sizes of the microlens. As materials to fabricate a microlens array, poly(dimethylsiloxane) and Norland Optical Adhesive 63 were adopted. The poly(dimethylsiloxane) microlens array exhibited higher total transmittance and higher diffuse transmittance, further enhancing the effective optical path and light extinction in material stacks for organic photovoltaics. This resulted in more current generation in an organic photovoltaic device with a poly(dimethylsiloxane) microlens array than in a Norland Optical Adhesive 63 microlens array. The sizes of the microlenses were controlled from 0.5 to 10 μm. The optical characteristics of microlens array films and material stacks with microlenses generally increased with size of the microlens, leading to a 10.6% and 16.0% improvement in the light extinction and power-conversion efficiency, respectively. In addition, electron and current generation in material stacks for organic photovoltaics were calculated from light extinction. The theoretical current generation matched well with experimental values derived from organic photovoltaic devices. Thus, the optical characterization of physical structures helps to predict how much more current can be generated in organic photovoltaic cells with a certain physical structure; it can also be used for screening the physical structures of organic photovoltaic cells.Heterojunction copper-zinc oxide catalysts were prepared by a hybrid two-step methodology comprising hydrothermal growth of ZnO nanorods (ZnO-NR) followed by deposition of Cu2O nanoparticles using an advanced gas deposition technique (AGD). The obtained bicatalysts were characterized by SEM, AFM, XRD, XPS, PL and spectrophotometry and revealed well-dispersed and crystalline Cu2O nanoparticles attached to the ZnO-NR. The adsorption properties and photocatalytic degradation of Orange II dye in water solutions were measured. It was found that the bicatalysts exhibited a conversion rate and quantum yield that both were about 50% higher compared with ZnO-NR alone, which were attributed to the intrinsic electric field created at the p-n junction formed at the Cu2O/ZnO interface facilitating charge separation of electron-hole pairs formed upon interband photon absorption. The interpretation was evidenced by efficient quenching of characteristic deep level ZnO photoluminescence bands and photoelectron core-level energy shifts. By comparisons with known energy levels in Cu2O and ZnO, the effect was found to be most pronounced for the non-polar ZnO-NR side facets, which accounted for about 95% of the exposed surface area of the catalyst and hence the majority of dye adsorption. It was also found that the dye adsorption capacity of the ZnO nanorods increased considerably after Cu2O deposition thereby facilitating the oxidation of the dye. The results imply the possibility of judiciously aligning band edges on structurally controlled and well-connected low-dimensional semiconductor nanostructures using combined two-step synthesis techniques, where in particular vacuum-based techniques such as AGD allow for growth of well-connected nanocrystals with well developed heterojunction interfaces.Antibiotic resistance is an emerging threat to public health. The development of a new generation of antimicrobial compounds is therefore currently required. Here we report a novel antimicrobial polymer of chitosan/polypropylene carbonate nanoparticles (CS/PPC NPs). These were designed and synthesized from readily available chitosan and a reactive oligomer polypropylene carbonate (PPC)-derived epoxy intermediate. By employing a simple and efficient functionalized strategy, a series of micelle-like chitosan-graft-polypropylene carbonate (CS-g-PPC) polymers and chitosan-polypropylene carbonate (CS-PPC) microgels were prepared by reacting mono-/bis-epoxy capped PPC with chitosan. The chemical structure, particle size, and surface charge of the newly synthesized polymers were characterized by infrared (IR) spectroscopy, nuclear magnetic resonance (NMR) spectroscopy, dynamic light scattering (DLS), and zeta potential measurements. The antimicrobial activities of these nanoparticles were determined in both Gram-positive bacteria (S. aureus) and Gram-negative bacteria (E. coli). Minimum inhibitory concentration (MIC), the nanoparticle concentration needed to completely inhibit the bacterial growth, was found at 128 μg mL-1 to 1024 μg mL-1, strongly depending both on the nature of the epoxy-imine network formed from the functional groups (mono- or bis-capped epoxy groups reacting with amine groups) and the feed ratio of the functional groups (-epoxy/-NH2) between the functionalized PPC and chitosan. No hemolysis was observed at concentrations well in excess of the effective bacteria-inhibiting concentrations. These findings provide a novel strategy to fabricate a new type of nanoantibiotic for antimicrobial applications.To eliminate the increasing adverse effects of electromagnetic pollution in everyday life, the shielding abilities of ferrite nanoparticles, multiwalled carbon nanotubes, and graphene oxide based hybrid composites have been investigated. The conceivable applications of the best investigated shielding composite samples on wearable and construction materials were investigated. Zinc substituted nickel and cobalt ferrite nanoparticles were synthesized using a sol-gel method with average crystallite size of 15-20 nm and incorporated with MWCNT and MWCNT-GO in a 1  1 weight ratio. Detailed investigations have been done on the prepared nano-composites by using X-ray diffraction, scanning and transmission electron microscopy, Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis, magnetic hysteresis loops, and vector network analysis. The microwave shielding capacity of the multiwalled carbon nanotube-zinc doped cobalt ferrite-graphene oxide hybrid composite was significantly enhanced up to 81.6 dB for the thickness of 2.4 mm in the X-band frequency region. Such a high SE indicates attenuation of the entire incoming EM radiation, which corroborates the potential of these materials in terms of high efficiency, tuneable, stable, and lightweight shielding applications. The synthesized MWCNT-CZFO-GO nanocomposite was used as an absorbent and was incorporated with cotton fabric, camouflage fabric, cement, and gypsum for high-efficiency daily life radiation shielding applications. These incorporated shielding samples (52.3 dB for cement, 31.4 dB for gypsum, 40.8 dB for camouflage fabric, and 28.6 dB for cotton fabric) showed a high attenuation capacity with more than 99.999% attenuation of the incident EM radiation establishing a promising behaviour to neutralize the harmful effects of radiation in day-to-day life.