Morphology versus Vertical Phase Segregation in Solvent Annealed Small Molecule Bulk Heterojunction Organic Solar Cells

The deep study of solvent annealed small molecules bulk heterojunction organic solar cells based on DPP(TBFu)2 : PC60BM blend is carried out. To reveal the reason of the solvent annealing advantage over the thermal one, capacitance-voltage measurements were applied. It was found that controlling the vertical phase segregation in the solar cells a high fullerene population in the vicinity of the cathode could be achieved. This results in increase of the shunt resistance of the cell, thus improving the light harvesting efficiency

The Sariçiçek Howardite Fall in Turkey: Source Crater of HED Meteorites on Vesta and İmpact Risk of Vestoids

The Sariçiçek howardite meteorite shower consisting of 343 documented stones occurred on 2 September 2015 in Turkey and is the first documented howardite fall. Cosmogenic isotopes show that Sariçiçek experienced a complex cosmic ray exposure history, exposed during ~12–14 Ma in a regolith near the surface of a parent asteroid, and that an ~1 m sized meteoroid was launched by an impact 22 ± 2 Ma ago to Earth (as did one third of all HED meteorites). SIMS dating of zircon and baddeleyite yielded 4550.4 ± 2.5 Ma and 4553 ± 8.8 Ma crystallization ages for the basaltic magma clasts. The apatite U-Pb age of 4525 ± 17 Ma, K-Ar age of ~3.9 Ga, and the U,Th-He ages of 1.8 ± 0.7 and 2.6 ± 0.3 Ga are interpreted to represent thermal metamorphic and impact-related resetting ages, respectively. Petrographic, geochemical and O-, Cr- and Tiisotopic studies confirm that Sariçiçek belongs to the normal clan of HED meteorites. Petrographic observations and analysis of organic material indicate a small portion of carbonaceous chondrite material in the Sariçiçek regolith and organic contamination of the meteorite after a few days on soil. Video observations of the fall show an atmospheric entry at 17.3 ± 0.8 kms-1 from NW, fragmentations at 37, 33, 31 and 27 km altitude, and provide a pre-atmospheric orbit that is the first dynamical link between the normal HED meteorite clan and the inner Main Belt. Spectral data indicate the similarity of Sariçiçek with the Vesta asteroid family (V-class) spectra, a group of asteroids stretching to delivery resonances, which includes (4) Vesta. Dynamical modeling of meteoroid delivery to Earth shows that the complete disruption of a ~1 km sized Vesta family asteroid or a ~10 km sized impact crater on Vesta is required to provide sufficient meteoroids ≤4 m in size to account for the influx of meteorites from this HED clan. The 16.7 km diameter Antonia impact crater on Vesta was formed on terrain of the same age as given by the 4He retention age of Sariçiçek. Lunar scaling for crater production to crater counts of its ejecta blanket show it was formed ~22 Ma ago

CO₂ Hydrogenation to Renewable Methane on Ni/Ru Modified ZSM-5 Zeolites: The Role of the Preparation Procedure

Mono- and bimetallic Ni- and Ru-modified micro-mesoporous ZSM-5 catalysts were prepared by wet impregnation. The influence of the Ni content, the addition of Ru and the sequence of the modification by two metals on the physicochemical properties of the catalysts were studied. They were characterized by X-ray powder diffraction (XRD), N2 physisorption, temperature-programmed reduction (TPR-TGA), TEM and XPS spectroscopy. Formation of finely dispersed nickel and/or ruthenium oxide species was observed on the external surface and in the pores of zeolite support. It was found that the peculiarity of the used zeolite structure and the modification procedure determine the type of formed metal oxides, their dispersion and reducibility. XPS study revealed that the surface became rich in nickel and poorer in ruthenium for bimetallic catalysts. Ni had higher dispersion in the presence of ruthenium, and TPR investigations also confirmed its facilitated reducibility. The studied catalysts were tested in CO2 hydrogenation to methane. 10Ni5RuZSM-5 material showed the highest activity and high selectivity for methane formation, reaching the equilibrium conversion and 100% selectivity at 400 °C. Stability and reusability of the latter catalyst show that it is appropriate for practical application

Synthesis and Properties of Magnetic Iron Oxide/Platinum Nanocomposites

Iron oxide/platinum nanocomposites have been synthesized by the extractive-pyrolytic method (EPM) involving gradual decomposition of iron capronate and n-trioctylammonium hexachloroplatinate initially produced by solvent extraction. The content of platinum in the composites was 1.2 wt%, 2.4 wt% and 4.8 wt%. Phase composition, morphology and magnetic properties of the produced materials were investigated. XRD analysis and magnetic measurements show that the magnetic phase (magnetite Fe3O4) dominates in a carrier sample produced by the pyrolysis of iron carboxylate, but hematite α-Fe2O3 exists there as an admixture. Referring to the TEM results, the produced composites contain ultra-disperse platinum particles on the carrier, and the mean size of these varies from 3 nm to 9 nm

Chlorhexidine–Silver Nanoparticle Conjugation Leading to Antimicrobial Synergism but Enhanced Cytotoxicity

This study explored the potential synergism within chlorhexidine–silver nanoparticle conjugates against Influenza type A, Staphylococcus aureus, Escherichia coli, and Candida albicans. Silver nanoparticles (SN) were obtained by the reduction of silver ions with green tea total phenolic extract and conjugated with chlorhexidine (Cx). The particles were characterized by UV-Vis and FTIR spectroscopies, dynamic light scattering, X-ray diffraction, and transmission electron microscopy. A stable negatively charged nano-silver colloid (ζ = −50.01) was obtained with an average hydrodynamic diameter of 92.34 nm. In the presence of chlorhexidine, the spectral data and the shift of the zeta potential to positive values (ζ = +44.59) revealed the successful sorption of the drug onto the silver surface. The conjugates (SN-Cx) demonstrated potentiation in their effects against S. aureus and C. albicans and synergism against E. coli with minimal inhibitory concentrations of SN at 5.5 µg/mL + Cx 8.8 µg/mL. The SN showed excellent virucidal properties, increasing with time, and demonstrated low toxicity. However, the coupling of the cationic chlorhexidine with nano-silver did not reduce its intrinsic cytotoxicity on various cell lines (MDCK, BJ, and A549). The newly synthesized antimicrobial agent exhibited an extended and promising therapeutic spectrum and needs to be further evaluated regarding the designated route of administration in three-dimensional cell models (e.g., nasal, bronchial, dermal, ocular, etc.)

Mesoporous Ce-Fe-Ni nanocomposites encapsulated in carbon-nanofibers: Synthesis, characterization and catalytic behavior in oxygen evolution reaction

16 figures, 6 tables.-- Supplementary material available.Ceria-iron oxide mesoporous materials with Fe:Ce molar ratio of 5:5 and 9:1 were synthesized by hydrothermal method using CTAB as a template and subsequently modified with NiO (molar ratio Ni:Fe = 1:2) by incipient wetness impregnation technique. In order to increase the electro-capacitive properties and reduce the intrinsic impedance of the metal oxides, the samples were consecutively modified by reduction in hydrogen to obtain highly dispersed Ni–Fe alloys into ceria matrix. By exploiting the high permeability of carbon inside ferrous alloys, the metal phase has been further modified into ferrous carbides and metal alloys encapsulated within carbon nanofibers. For this purpose, a reaction, already widely studied for the production of hydrogen, was used, that is the decomposition of methanol vapors. In fact, this decomposition, in addition to producing syn-gas and methane, changes the catalysts in use through a chemical vapor deposition-carbon coating process. This fact, has been used by us to demonstrate how the newly obtained metal-carbon nanocomposites can be used for electro-catalytic purposes. The modified phases of the two molar ratios of the Fe–Ni–Ce catalysts were tested in the Oxygen Evolution Reaction (OER) in an alkaline environment (1 M KOH), showing a satisfactory and progressive increase in activity and a surprising decrease in the overpotential at 10 mA/cm2 of current density. The morphological, textural and physicochemical properties of the samples were characterized in details by XRD, N2-physisorption, TG-TPO, TEM, EDX, FTIR, XPS, Raman and Moessbauer spectroscopies.This research was funded by the BIKE project, which received funding from the European Union's Horizon 2020 research and innovation program under the Marie Sklodowska-Curie grant agreement no. 813748.Peer reviewe

Promotional Effect of Gold on the WGS Activity of Alumina-Supported Copper-Manganese Mixed Oxides

The water-gas shift (WGS) reaction is a well-known industrial process used for the production of hydrogen. During the last few decades, it has attracted renewed attention due to the need for high-purity hydrogen for fuel-cell processing systems. The aim of the present study was to develop a cost-effective and catalytically efficient formulation that combined the advantageous properties of transition metal oxides and gold nanoparticles. Alumina-supported copper- manganese mixed oxides were prepared by wet impregnation. The deposition-precipitation method was used for the synthesis of gold catalysts. The effect of the Cu:Mn molar ratio and the role of Au addition on the WGS reaction’s performance was evaluated. Considerable emphasis was put on the characterization of the as-prepared and WGS-tested samples by means of a number of physicochemical methods (X-ray powder diffraction, high-resolution transmission electron microscopy, electron paramagnetic resonance, X-ray photoelectron spectroscopy, and temperature-programmed reduction) in order to explain the relationship between the structure and the reductive and WGS behavior. Catalytic tests revealed the promotional effect of gold addition. The best performance of the gold-promoted sample with a higher Cu content, i.e., a Cu:Mn molar ratio of 2:1 might be related to the beneficial role of Au on the spinel decomposition and the highly dispersed copper particle formation during the reaction, thus, ensuring the presence of two highly dispersed active metallic phases. High-surface-area alumina that was modified with a surface fraction of Cu⁻Mn mixed oxides favored the stabilization of finely dispersed gold particles. These new catalytic systems are very promising for practical applications due to their economic viability because the composition mainly includes alumina (80%)

Gold-Based Catalysts for Complete Formaldehyde Oxidation: Insights into the Role of Support Composition

Formaldehyde (HCHO) is recognized as one of the most emitted indoor air pollutants with high detrimental effect on human health. Significant research efforts are focused on HCHO removal to meet emission regulations in an effective and economically profitable way. For over three decades, the unique electronic properties and catalytic abilities of nano-gold catalysts continue to be an attractive research area for the catalytic community. Recently, we reported that mechanochemical mixing is a relevant approach to the preparation of Co-Ce mixed oxides with high activity in complete benzene oxidation. A trend of higher surface defectiveness, in particular, oxygen vacancies, caused by close interaction between cobalt oxide and cerium oxide phases, was observed for a mixed oxide composition of 70 wt.% Co3O4 and 30 wt.% CeO2. These results directed further improvement by promotion with gold and optimization of mixed oxide composition, aiming for the development of an efficient catalyst for room temperature HCHO abatement. Support modification with potassium was studied; however, the K addition caused less enhancement of HCHO oxidation activity than expected. This motivated the preparation of new carrier material. In addition to Co3O4-CeO2 mixed metal oxides with preset ratio, γ-Al2O3 intentionally containing 33% boehmite and shortly named Al2O3-b was used for synthesis. Analysis of the role of support composition in HCHO oxidation was based on the characterization of nano-gold catalysts by textural measurements, XRD, HRTEM, XPS, and TPR techniques. Gold supported on mechanochemically treated Co3O4-CeO2-Al2O3-b (50 wt.% Al2O3-b) exhibited superior activity owing to high Ce3+ and Co3+ surface amounts and the most abundant oxygen containing species with enhanced mobility. This catalyst achieved oxidation to CO2 and H2O by 95% HCHO conversion at room temperature and 100% at 40 °C, thus implying the potential of this composition in developing efficient catalytic materials for indoor air purification

Hydrodemethoxylation/Dealkylation on Bifunctional Nanosized Zeolite Beta

Mono-, and bimetallic Ni-, Ru-, and Pt-modified nanosized Beta zeolite catalysts were prepared by the post synthesis method and characterized by powder X-ray diffraction (XRD), nitrogen physisorption, HRTEM microscopy, temperature-programmed reduction (TPR-TGA), ATR FT-IR spectroscopy, and by solid-state MAS-NMR spectroscopy. The presence of nanosized nickel-oxide, ruthenium-oxide, and platinum species was detected on the catalysts. The presence of Brønsted and Lewis acid sites, and incorporation of nickel ions into zeolite lattice was proven by FT-IR of adsorbed pyridine. The structural changes in the catalyst matrix were investigated by solid state NMR spectroscopy. The catalysts were used in a gas-phase hydrodemethoxylation and dealkylation of 2-methoxy-4-propylphenol as a lignin derivative molecule for phenol synthesis