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We compared the impact of alumina doping on the structure of Al2O3–SiO2 amorphous thin films and bulk glasses using Raman spectroscopy and x‐ray diffraction. In both thin films and bulk glasses, the addition of Al2O3 is accompanied by an increase in the mean Si–O–T angle and an evolution of the ring statistics with a decrease in the proportion of small rings. We evidenced structural differences between sputtered films and fused bulk glasses. Sputtered Al2O3–SiO2 thin films are about 6%–7% denser than their equivalent Al2O3–SiO2 bulk glasses. This difference is mainly due to a change in ring statistics with the formation of small rings within the sputtered thin films. These structural differences in atomic structural organization highlight the impact of the synthesis conditions and open the door to further investigation of the structure–functional property relationships in sputtered Al2O3–SiO2 thin films. [ABSTRACT FROM AUTHOR]

The structural, microstructural, and magnetic properties of ~5‐nm‐sized Co0.6Zn0.4Fe2 − xGdxO4 nanoparticles were investigated in order to evaluate their capability to enhance the magnetic resonance imaging contrast as high magnetization agents. A focus was made on the solubility of Gd3+ cations within the spinel lattice. By coupling X‐ray diffraction to X‐ray fluorescence spectroscopy, we demonstrated that only a limited fraction of Gd3+ can substitute Fe3+ ions into the whole crystal structure and does not exceed 6 at.‐%. At this concentration, the room temperature (27°C) saturation magnetizations of the prepared superparamagnetic nanocrystals were found to be close to 80 emu g−1. Coating these nanoparticles with hydrophilic dopamine ligands leads to the formation of ~50‐nm‐sized clusters in water. As a consequence, relatively high r2/r1 ratios of transverse to longitudinal proton relaxivities and high r2 values were measured in the resulting colloids at physiological temperature (37°C) for an applied magnetic field of 1.41 T: 33 and 188 mM−1 sec−1, respectively, for the richest system in gadolinium. Moreover, after incubation with healthy human model cells (fibroblasts) at doses as high as 10 μg mL−1, they induce neither cellular death nor acute cellular damage making the engineered probes particularly valuable for negative magnetic resonance imaging contrasting. [ABSTRACT FROM AUTHOR]

This report presents the fabrication of bifunctional magnetic and fluorescent microneedles (µNDs) made of a ternary mixture of magnetic nanoparticles (NPs), quantum dots (QDs), and polyelectrolyte. The assembly relies on the electrostatic complexation of negatively charged NPs with positively charged polymer strands and is controlled by the charge ratio between the nanoparticle building blocks and the polymer mortar. The resulting 1D objects can be actuated using an external magnetic field and can be imaged using fluorescence microscopy, thanks to the fluorescent and superparamagnetic properties inherited from their NP constituents. Using a combination of core and surface characterizations and a state-of-the-art image analysis algorithm, the dependence of the brightness and length on the ternary composition is thoroughly investigated. In particular, statistics on hundreds of µNDs with a range of compositions show that the µNDs have a log-lormal length distribution and that their mean length can be robustly tuned in the 5-50 µm range to match the relevant length scales of various applications in micromixing, bioassays or biomechanics. [ABSTRACT FROM AUTHOR]

Clay/mercaptosuccinic acid hybrids were prepared through radical thiol-ene coupling between methacrylate-silanized clay and mercaptosuccinic acid. The clay surface was modified by 3-trimethoxysilylpropylmethacrylate, then mercaptosuccinic acid was clicked by ultraviolet (UV)-triggered thiol-ene addition reaction at 365 nm. Pristine and modified clays were characterized by X-ray diffraction (XRD), attenuated total reflection (ATR) and XPS. The clay/mercaptosuccinic acid material was employed as an adsorbent for the removal of Pb(II) from aqueous solutions. Kinetic studies indicated that the adsorption of Pb(II) followed the pseudo-first-order equation while the Langmuir model fitted the adsorption isotherm. The maximum adsorption was found to be 74.7 mg/g for an equilibrium time of ~80 min. UV-triggered thiol-ene reaction is demonstrated to be an easy and elegant pathway for designing reactive and functional clay for environmental and other applications. Copyright © 2016 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]

The increasing production of nanoparticles has raised strong concerns regarding their environmental release. In life cycle scenarios of nanoparticles, marine systems constitute one of the main final compartments, and the fate of nanoparticles in marine environments needs to be assessed. The dissolution kinetics of commercial uncoated and organic-coated ZnO nanoparticles in synthetic seawater were investigated using the Donnan membrane technique and 1000-Da pore size ultrafiltration. Uncoated nanoparticles reach a maximum dissolution within the first hour, approximately 24% of total ZnO at pH 8.2, and 4% at pH 7.7, followed by secondary carbonated phase precipitation (hydrozincite) until the system reaches a steady state after 30 d of interaction. Assuming a pseudo first-order kinetics for hydrozincite precipitation allowed calculation of kinetics constant values k′p of −208 × 10−4 mol L−1 h−1 ± 15 × 10−4 mol L−1 h−1 (standard deviation) at pH 7.7, and −57 × 10−4 mol L−1 h−1 ± 11 × 10−4 mol L−1 h−1 at pH 8.2. The presence of an organic coating drastically modifies the life cycle of nanoparticles, with a maximum dissolution reached after 7 d of interaction, followed by a stationary phase lasting from 1 wk to 3 wk, and a subsequent Zn carbonate precipitation until a steady state is reached after 1.5 mo. Monitoring changes in the physicochemical parameters of nanoparticles after exposure to synthetic seawater constitutes an important step in predicting their fate in environmental systems, with major implications for ecotoxicological studies in which metallic speciation is required for toxicity evaluation. Environ Toxicol Chem 2014;33:341-349. © 2013 SETAC [ABSTRACT FROM AUTHOR]

We report the synthesis of yttrium iron garnet ( YIG) combining soft chemistry route, namely the polyol process, and spark plasma sintering ( SPS) technique. The polyol process produced an intermediary amorphous phase containing both iron and yttrium cations in the desired ratio. They were annealed at 400°C in air to decompose the organic content of the reaction (polyol and acetate). To achieve the garnet phase, the polyol-obtained precursor was subjected to reactive SPS treatment at a temperature of 750°C, far below the typical temperatures (1350°C) used in the classic solid-state reaction process. In 15 min pure and high-density Y3 Fe5 O12 ceramic, with about 100 nm sized crystalline grains, was obtained. We report as well the characterization of the initial amorphous phase and the obtained YIG by X-ray diffraction, scanning electron microscopy, Fourier-transform infrared spectroscopy, 57 Fe Mössbauer spectrometry, and magnetization measurements. [ABSTRACT FROM AUTHOR]

In article number 1802136 Cédric Boissière, Cédric Tard, Jennifer Peron and co‐workers present the synthesis of ultra porous nanostructured iridium‐based microspheres using a cheap and easily scalable water‐based process. These hierarchical catalysts are active and stable towards the oxygen evolution reaction. They are easily processed to make percolated and highly porous anode catalyst layers that are ideal for gas, water, proton and electrons transport when integrated into the proton exchange membrane of electrolysis cells. [ABSTRACT FROM AUTHOR]

Iridium oxide is the gold‐standard catalyst for the oxygen evolution reaction (OER) in acidic media due to its unmatched activity and stability. Here, a new catalyst architecture comprising a nanoneedle network of iridium‐containing oxides assembled into macroporous micrometric particles with ≈75% of porosity is reported. The rationally designed porous hierarchical structure optimizes the accessibility of reactants and products to the surface of the nanoparticles and maximizes catalyst activity. The materials are easily prepared from aqueous solutions by an industrially viable spray‐drying route through an evaporation self‐assembly mechanism. The versatility of the process enables the preparation of mixed oxides with low iridium content, particles with tunable crystallinity, and various iridium surface species with high electrochemical activity. Highly porous Ir0.7Ru0.3O2 outperforms commercial iridium oxide. These materials also represent an ideal platform to assess the reactivity of the iridium and oxygen species involved in the oxygen evolution reaction. Furthermore, it is demonstrated that these highly porous particles are optimal building blocks to be integrated into catalyst layers, without the drawbacks associated with the use of discrete nanoparticles. Fresh‐ and end‐of‐test membrane–electrode assemblies' characterization shows that their particular architecture is preserved upon catalyst layer preparation and after operation in a proton‐exchange membrane electrolysis cell. Ultraporous nanocrystalline IrOx microspheres are optimal architectures to build highly porous catalyst layers. Easily prepared by a spray‐drying process, they consist of a nanoneedle network of iridium‐containing oxides assembled into macroporous micrometric particles with ≈75% of porosity. While being very active toward the oxygen evolution reaction, their morphology is maintained when assembled and tested in a proton exchange membrane electrolysis cell. [ABSTRACT FROM AUTHOR]