The rational design of multifunctional catalysts that use non-noble metals to facilitate the interconversion between H2, O2, and H2O is an intense area of investigation. Bimetallic nanosystems with highly tunable electronic, structural, and catalytic properties that depend on their composition, structure, and size have attracted considerable attention. Herein, we report the synthesis of bimetallic nickel–copper (NiCu) alloy nanoparticles confined in a sp2 carbon framework that exhibits trifunctional catalytic properties toward hydrogen evolution (HER), oxygen reduction (ORR), and oxygen evolution (OER) reactions. The electrocatalytic functions of the NiCu nanoalloys were experimentally and theoretically correlated with the composition-dependent local structural distortion of the bimetallic lattice at the nanoparticle surfaces. Our study demonstrated a downshift of the d-band of the catalysts that adjusts the binding energies of the intermediate catalytic species. XPS analysis revealed that the binding energy for Ni 2p3/2 band of the Ni0.25Cu0.75/C nanoparticles was shifted ∼3 times compared to other bimetallic systems, and this was correlated to the high electrocatalytic activity observed. Interestingly, the bimetallic Ni0.25Cu0.75/C catalyst surpassed the OER performance of RuO2 benchmark catalyst exhibiting a small onset potential of 1.44 V vs RHE and an overpotential of 400 mV at 10 mA·cm–2 as well as the electrochemical long-term stability of commercial RuO2 and Pt catalysts and kept at least 90% of the initial current applied after 20 000 s for the OER/ORR/HER reactions. This study reveals significant insight about the structure–function relationship for non-noble bimetallic nanostructures with multifunctional electrocatalytic properties.

Biodiversity hotspots understandably attract considerable conservation attention. However, deserts are rarely viewed as conservation priority areas, due to their relatively low productivity, yet these systems are home to unique species, adapted to harsh and highly variable environments. While global attention has been focused on hotspots, the world's largest tropical desert, the Sahara, has suffered a catastrophic decline in megafauna. Of 14 large vertebrates that have historically occurred in the region, four are now extinct in the wild, including the iconic scimitar-horned oryx (Oryx dammah). The majority has disappeared from more than 90% of their Saharan range, including addax (Addax nasomaculatus), dama gazelle (Nanger dama) and Saharan cheetah (Acinonyx jubatus hecki) -all now on the brink of extinction. Greater conservation support and scientific attention for the region might have helped to avert these catastrophic declines. The Sahara serves as an example of a wider historical neglect of deserts and the human communities who depend on them. The scientific community can make an important contribution to conservation in deserts by establishing baseline information on biodiversity and developing new approaches to sustainable management of desert species and ecosystems. Such approaches must accommodate mobility of both people and wildlife so that they can use resources most efficiently in the face of low and unpredictable rainfall. This is needed to enable governments to deliver on their commitments to halt further degradation of deserts and to improve their status for both biodiversity conservation and human well-being. Only by so-doing will deserts be able to support resilient ecosystems and communities that are best able to adapt to climate change.

No abstract

This work reports the synthesis at room temperature of transparent and colored W(x)Si(y)O(z) thin films by magnetron sputtering (MS) from a single cathode. The films were characterized by a large set of techniques including X-ray photoelectron spectroscopy (XPS), Rutherford backscattering spectrometry (RBS), Fourier transform infrared (FT-IR), and Raman spectroscopies. Their optical properties were determined by the analysis of the transmission and reflection spectra. It was found that both the relative amount of tungsten in the W-Si MS target and the ratio O(2)/Ar in the plasma gas were critical parameters to control the blue coloration of the films. The long-term stability of the color, attributed to the formation of a high concentration of W(5+) and W(4+) species, has been related with the formation of W-O-Si bond linkages in an amorphous network. At normal geometry (i.e., substrate surface parallel to the target) the films were rather compact, whereas they were very porous and had less tungsten content when deposited in a glancing angle configuration. In this case, they presented outstanding electrochromic properties characterized by a fast response, a high coloration, a complete reversibility after more than one thousand cycles and a relatively very low refractive index in the bleached state.

Fluorescent tetracationic porphyrin (TMPyP) molecules have been incorporated into optically transparent TiO(2) thin films acting as a host material. The films, with a columnar structure and open pores, were prepared by electron evaporation at glancing angles (GAPVD). The open porosity of the films has been estimated by measuring a water adsorption isotherm with a quartz crystal monitor. TMPyP molecules were infiltrated in the host thin films by their immersion into water solutions at controlled values of pH. The state of the adsorbed molecules, the infiltration efficiency, and the adsorption kinetics were assessed by analyzing the optical response of the films by UV-vis absorption and fluorescence techniques. The infiltration efficiency was directly correlated with the acidity of the medium, increasing at basic pHs as expected from simple considerations based on the concepts of the point of zero charge (PZC) developed for colloidal oxides. By a quantitative evaluation based on the analysis of the UV spectra, the infiltration process has been described by a Langmuir type adsorption isotherm and an Elovich-like kinetics. The accessibility of the infiltrated molecules in the TMPyP/TiO(2) composite films is assessed by following the changes of their optical properties when exposed to the acid vapors and their subsequent recovery with time.

The oxygen reduction (ORR) and hydrogen evolution (HER) reactions are the most important cathodic processes involved in fuel cell and water splitting, respectively.

The magnetically assisted removal of fatty acids from organic solutions and vegetable oils using iron oxide magnetic nanoparticles (MNPs) was investigated. The effect of contact time and concentration on the adsorption of oleic acid from ethanol-hexane solutions was investigated at room temperature using equilibrium batch experiments. The results showed that the adsorption is rapid (<2 h) and follows a pseudo-second-order model. The adsorption isotherm was found to follow the Langmuir model and the maximum adsorption capacity of oleic acid was determined to be 125 mg g −1 . FTIR analyses of the magnetically separated MNPs demonstrated the covalent binding of the carboxylic group to the particle surface in a bidentate/bridging manner. Thermogravimetric analyses showed that the adsorption capacity of MNPs is very similar for the most common fatty acids in vegetable oils ( palmitic, stearic, oleic and linoleic acids). Desorption of fatty acids was readily achieved upon basic treatment and the regenerated magnetite nanoparticles were found to be recyclable for repeated use. The separation of fatty acids from olive and sunflower oils was investigated without added solvent. MNPs were found to remove up to 85% of the fatty acids in the oil within 2 h with a 10 wt% load at room temperature, without alteration of the pigment composition.

a b s t r a c tTetracationic porphyrin (TMPyP) molecules were incorporated into an optically transparent TiO 2 thin film, prepared by Glancing Angle Physical Vapour Deposition (GAPVD), by simple infiltration (at pH 6.4). The preparation of optically transparent TMPyP/TiO 2 composite thin films provides a method for the integration of the porphyrin molecules into photonic devices for direct monitoring of gases. Previously, UV-visible and fluorescence spectral techniques have been used to study the reversible protonation of TMPyP in aqueous solution. The optical spectrum of TMPyP shows an intense Soret band at 423 nm with a 22 nm red shift upon protonation by HCl. The experimental conditions for monitoring the concentration of HCl gas by absorption spectroscopy have been optimized. The maximum absorbance change was observed at the Soret band wavelength. A selected temperature of 80 • C and a 300 s recovery period were found to be the optimum operating parameters (response time t 50 = 16.8 ± 0.7 s). The composite with smaller surface concentration of TMPyP ( = 0.3 × 10 −9 mol cm −2 ) presented the best detection limit (0.1 ppm). The response of the composite sensor was highly stable for several months.