Development of Highest Value of the Measured Efficiency of Mesoporous Petal Shaped Europium (III) Doped Cobalt Tetroxide@Cupric Oxide Hybrid Nanomaterials for Enhanced Room Temperature Photoluminescence and Fluorescence Decay Properties.

In our work, a novel series of europium (III) (Eu3+) (5, 10 and 15 wt %) doped cobalt tetroxide@cupric oxide (Co3O4@CuO) nanomaterials (NMs) were synthesized by facile coprecipitation method. The synthesized NMs were characterized by XRD (X-ray diffraction), FT-IR (Fourier transform infrared), UV (ultraviolet)-visible absorption spectra, XPS (X-ray photoelectron), BET (Brunauer-Emmett-Teller) analytical methods. Crystal structure studies revealed the formation of polycrystalline nature with monoclinic and cubic phase. The morphology studies of Eu3+x:Co3O4@CuO (x = 5, 10 and 15 wt %) showed petal shape nanoparticles (NPs) with agglomeration. Redshift in optical absorption spectra appeared with a significant impact on the optical band gap as Eu3+ concentration increases on Co3O4@CuO bimetallic oxide NMs. The chemical composition and valence state of the elements confirmed from XPS studies detected the presence of Eu, Cu, Co, O and C elements. An increase in the pore size and surface area resulted as the Eu3+ concentration increased on Co3O4@CuO NMs. However, room temperature photoluminescence (RTPL) spectra of Co3O4@CuO bimetallic oxide NMs at two different excitations (λ excitation = 280 nm, 320 nm) showed sharp, strong emission intensities located at near ultraviolet (NUV) region and weak emissions detected at far ultraviolet (FUV) regions of the RTPL spectrum. Further, visible range emission intensities were displayed by Eu3+:Co3O4@CuO (5, 10 and 15 wt %) NMs when exited at 280 nm. The characteristic white light emission peaks in the visible range of the RTPL spectra showed intense blue, green and orange colours. Emission intensity increases with an increase in Eu3+ concentration on Co3O4@CuO bimetallic oxide NMs. The fluorescence (FL) decay spectra of Eu3+ 10wt% and 15 wt%: Co3O4@CuO NMs showed a decay lifetime of 2.54 and 2.31 ns (ns) attributed to the dynamic, ultrafast excitation energy transfer between Eu3+ (dopant) and Co3O4@CuO (host) NMs. It is proposed that enhanced RTPL emission intensity and FL decay behavior of Eu3+x:Co3O4@CuO NMs closely related to the change in the optical band gap, variation in the crystallite size, formation of more number of oxygen vacancies in the crystal structure of hybrid nanomaterials.

Effect of Ag content on the nanostructure and antimicrobial activity of CeO2.

The morphological and antibacterial effects of CeO2 nanoparticles (NPs) with different amounts of Ag precursor were studied. The samples were synthesized with different percentages of silver nitrate content by co-precipitation method. The cerium nitrate hexahydrate was a precursor of Ce reagent, polyvinylpyrrolidone as dispersant agent, and ammonium hydroxide as a precipitating agent. The obtained particles were annealed at 400 °C and characterized by X-ray diffraction, scanning electron microscope (SEM), transmission electron microscopy (TEM), and N2 physisorption. The particles show high crystallinity, whose size decreases slightly by the effect of Ag precursor incorporation. These particle morphologies studied by SEM and TEM revealed the spherical shape of CeO2 NPs. Furthermore, the Ag particles were observed with a size of around 30 nm. Selected area electron diffraction patterns confirm the cubic structure of CeO2, also the cubic structure of Ag particles. Besides, it was determined that Ag incorporation has no significant influence on the textural properties of NPs. In addition, the antibacterial activity was evaluated against gram-negative and gram-positive microorganisms. The quantitative results showed that the antimicrobial activity increased depending on the Ag amount incorporated, reaching up to 99.999% of the growing reduction rate.

Facile Construction of Porous ZnMn2O4 Hollow Micro-Rods as Advanced Anode Material for Lithium Ion Batteries.

Spinel ZnMn2O4 is considered a promising anode material for high-capacity Li-ion batteries due to their higher theoretical capacity than commercial graphite anode. However, the insufficient cycling and rate properties seriously limit its practical application. In this work, porous ZnMn2O4 hollow micro-rods (ZMO HMRs) are synthesized by a facile co-precipitation method coupled with annealing treatment. On the basis of electrochemical analyses, the as-obtained samples are first characterized by X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, and scanning electron microscopy techniques. The influences of different polyethylene glycol 400 (PEG 400) additions on the formation of the hollow rod structure are also discussed. The abundant multi-level pore structure and hollow feature of ZMO HMRs effectively alleviate the volume expansion issue, rendering abundant electroactive sites and thereby guaranteeing convenient Li+ diffusion. Thanks to these striking merits, the ZMO HMRs anode exhibits excellent electrochemical lithium storage performance with a reversible specific capacity of 761 mAh g-1 at a current density of 0.1 A g-1, and a long-cycle specific capacity of 529 mAh g-1 after 1000 cycles at 2.0 A g-1 and keep a remarkable rate capability. In addition, the assembled ZMO HMRs-based full cells deliver an excellent rate capacity, and when the current density returns to 0.05 A g-1, the specific capacity can still reach 105 mAh g-1 and remains at 101 mAh g-1 after 70 cycles, maintaining a material-level energy density of approximately 273 Wh kg-1. More significantly, such striking electrochemical performance highlights that porous ZMO HMRs could be a promising anode candidate material for LIBs.

Biologic Impact of Green Synthetized Magnetic Iron Oxide Nanoparticles on Two Different Lung Tumorigenic Monolayers and a 3D Normal Bronchial Model-EpiAirwayTM Microtissue.

The present study reports the successful synthesis of biocompatible magnetic iron oxide nanoparticles (MNPs) by an ecofriendly single step method, using two ethanolic extracts based on leaves of Camellia sinensis L. and Ocimum basilicum L. The effect of both green raw materials as reducing and capping agents was taken into account for the development of MNPs, as well as the reaction synthesis temperature (25 °C and 80 °C). The biological effect of the MNPs obtained from Camellia sinensis L. ethanolic extract (Cs 25, Cs 80) was compared with that of the MNPs obtained from Ocimum basilicum L. ethanolic extract (Ob 25, Ob 80), by using two morphologically different lung cancer cell lines (A549 and NCI-H460); the results showed that the higher cell viability impairment was manifested by A549 cells after exposure to MNPs obtained from Ocimum basilicum L. ethanolic extract (Ob 25, Ob 80). Regarding the biosafety profile of the MNPs, it was shown that the EpiAirwayTM models did not elicit important viability decrease or significant histopathological changes after treatment with none of the MNPs (Cs 25, Cs 80 and Ob 25, Ob 80), at concentrations up to 500 µg/mL.

Engineering atorvastatin loaded Mg-Mn/LDH nanoparticles and their composite with PLGA for bone tissue applications.

The impact of mixing method in conventional co-precipitation synthesis of layered double hydroxides (LDHs), on particle size, size distribution and drug loading capacity is reported. Synthesis of Mg (II)/Mn (III)-LDH nano-platelets was performed at constant pH using three different mixing systems, magnetic stirrer, mechanical mixer, and homogenizer at ambient temperature and a fixed Mg/Mn ratio of 3/1. The LDH characterization results showed that mechanical mixing and homogenization lead to production of very fine LDH nano-platelets (about 90-140 nm), with narrow particle size distribution. Amount of the intercalated drug was determined as about 60% and showed a significant increase in loading capacity of the LDH through homogenization and mechanical mixing compared to that of the magnetic stirring (about 35%). Our results also showed that in LDH preparation via co-precipitation, the mixing system plays a more influential role in particle size, size distribution, and drug loading control, than the mixing speed of each system. Drug loaded-LDH/PLGA composites were prepared via electrospinning to afford a bioactive/osteoinductive scaffold. A remarkable degree of cell viability on the scaffolds (drug-loaded-LDH/PLGA composite) was confirmed using MTT assay. Osteogenic differentiation of human ADMSCs, as shown by alkaline phosphatase activity and Alizarin Red staining assays, indicated that the scaffold with 5% drug loaded LDH(Mn-Mg-LDH/PLGA/AT5%) induced a remarkably higher level of the markers compared to the PLGA scaffold and therefore, it could be a valuable candidate for bone tissue engineering applications.

On Tailoring Co-Precipitation Synthesis to Maximize Production Yield of Nanocrystalline Wurtzite ZnS.

Pyroelectric materials can harvest energy from naturally occurring ambient temperature changes, as well as from artificial temperature changes, notably from industrial activity. Wurtzite- based materials have the advantage of being cheap, non-toxic, and offering excellent opto-electrical properties. Due to their non-centrosymmetric nature, all wurtzite crystals have both piezoelectric and pyroelectric properties. Nanocrystalline wurtzite ZnS, being a room temperature stable material, by contrast to its bulk counterpart, is interesting due to its still not well-explored potential in piezoelectric and pyroelectric energy harvesting. An easy synthesis method-a co-precipitation technique-was selected and successfully tailored for nanocrystalline wurtzite ZnS production. ZnS nanopowder with nanoparticles of 3 to 5 nm in size was synthesized in ethyl glycol under medium temperature conditions using ZnCl2 and thiourea as the sources of Zn and S, respectively. The purified and dried ZnS nanopowder was characterized by conventional methods (XRD, SEM, TEM, TG and FTIR). Finally, a constructed in-house pilot plant that is able to produce substantial amounts of wurtzite ZnS nanopowder in an environmentally friendly and cost-effective way is introduced and described.

A glassy carbon electrode modified with a nanocomposite prepared from Pd/Al layered double hydroxide and carboxymethyl cellulose for voltammetric sensing of hydrogen peroxide.

A Pd/Al layered double hydroxide/carboxymethyl cellulose nanocomposite (CMC@Pd/Al-LDH) was fabricated using carboxymethyl cellulose as a green substrate via co-precipitation method. The synthesized nanocomposite was characterized using different methods such as scanning electron microscopy, energy-dispersive X-ray spectroscopy, X-ray powder diffraction, transmission electron microscopy, and electrochemical techniques. A glassy carbon electrode (GCE) was then modified with the suspended composite to obtain an electrochemical sensor for hydrogen peroxide (H2O2). The voltammetric (cathodic) current of the modified GCE was measured at -380 mV (vs. Ag/AgCl), at the scan rate of 50 mV.s-1. Results show a linear dynamic range of 1 to 120 µM, and a 0.3 µM limit of detection (at S/N = 3). Intraday and interday relative standard deviations are in the ranges of 4.9-5.4% and 6.8-7.3%, respectively. The sensor was applied for the determination of H2O2 in basil extracts, milk, and spiked river water samples. The recoveries are between 96.60 and 102.30%. Graphical abstractA Pd/Al layered double hydroxide/carboxymethyl cellulose nanocomposite (CMC@Pd/Al-LDH) was fabricated via co-precipitation method and was characterized using scanning electron microscopy, Energy-dispersive X-ray spectroscopy, X-ray powder diffraction, transmission electron microscopy and electrochemical techniques. CMC@Pd/Al-LDH was used to fabricate H2O2 electrochemical sensor.

Nano-alumina powders/ceramics derived from aluminum foil waste at low temperature for various industrial applications.

In this work, nanoscale single crystalline γ- and α-alumina powders have been successfully prepared from aluminum foil waste precursor via co-precipitation method using NH4OH as a precipitant. The obtained gel after co-precipitation treatment, was calcined at different temperatures (500,700, 900, 1050, 1100, 1300 and 1500 °C) and the products were characterized by XRD, FTIR and HRTEM. The results revealed that nano-γ-Al2O3 was fully transformed to nanometer-sized α-Al2O3 (36-200 nm) after annealing at temperatures as low as 1100 °C.The thermally preheated powder at 500 °C was further pressed under 95 MPa by the uniaxial press and the obtained bodies were found to have98.82% of the theoretical density, 1.18% porosity and 708 MPa compressive strength, when sintered at temperatures as low as 1600 °C without using any sintering aid. These excellent results proved that this work will contribute to finding a commercial source for preparing sub 100 nm α-alumina through the secondary resources management and even more so to synthesizing strong α-Al2O3 bodies which are promising in terms of their structure and compression. The α-Al2O3 bodies synthesized by the present work could be used as a feedstock for fabrication of various kinds of functional and structural materials that are extensively used in high tech.

Photoluminescence and electron paramagnetic resonance properties of a potential phototherapic agent: MMgF4 :Gd3+ (M = Ba, Sr) sub-microphosphors.

Novel narrow band UVB-emitting phosphors, BaMgF4 :Gd3+ and SrMgF4 :Gd3+ phosphors, were synthesized using a co-precipitation synthesis method. X-Ray diffraction analysis was carried out to confirm compound formation, phase purity and crystallinity of the phosphor. At 274 nm excitation, phosphors show a sharp narrow band emission at 313 nm that can be assigned to 6 P7/2  â†’ 8 S7/2 transition of the Gd3+ ion. With increasing dopant concentration, intensity enhances and then decreases after a certain concentration, which is an indication of concentration quenching taking place in the phosphor. Scanning electron microscopy images of the phosphor show agglomerated particles in the sub-micron range. Particles range in size from 600 to 800 nm. Electron paramagnetic resonance studies of the phosphors were carried out to detect radicals present in the prepared phosphor. With narrow band UVB emission, phosphor seems to be a good candidate for UV phototherapy application. Copyright © 2016 John Wiley & Sons, Ltd.

Study of photocatalytic activity of ZnS quantum dots as efficient nanoparticles for removal of methyl violet: effect of ferric ion doping.

Zinc sulfide quantum dots (QDs), as pure and doped with Fe(3+), were prepared for photodecolorization of methyl violet (MV), as a model dye, under UV light irradiation. The syntheses of QDs were carried out using a simple chemical co-precipitation method. The prepared samples were characterized by various techniques including X-ray diffraction, transmission electron microscopy, UV-Vis spectrophotometry and flame atomic absorption spectroscopy. The influences of operational parameters on the decolorization of MV such as dopant content, pH, dosage of nanophotocatalyst, UV irradiation time and initial dye concentration were studied. The results showed that the QDs presented high efficiency for MV decolorization, and doping of ZnS QDs with Fe(3+) enhanced the efficiency and rate of dye removal. Finally, the reproducibility and kinetic model of the dye degradation were discussed.