Reduced graphene oxide–gold nanoparticle membrane for water purification

The reduced graphene oxide–gold nanoparticle (rGO–Au NP) membranes are prepared by vacuum filtration method. The sizes of the Au NPs on the surface of the rGO are about 8–10 nm, and the lattice spacing of Au NPs is 0.0241 nm, which is relative to the cubic lattice of the gold crystal. The layer-by-layer stacking structure of rGO–Au NP membrane can be observed clearly by field emission scanning electron microscopy. The water flux of the rGO–Au NP membrane is as high as 204.1 L m^?2 h^?1 bar^?1, and its retention for Rhodamine B (RhB) is as high as 99.79%.     

The development and challenges of rechargeable non-aqueous lithium–air batteries

Lithium–air (Li–air) batteries have recently received much attention due to their extremely high theoretical energy densities. The significantly larger theoretical energy density of Li–air batteries is due to the use of a pure lithium metal anode and the fact that the cathode oxidant, oxygen, is stored externally since it can be readily obtained from the surrounding air. However, before Li–air batteries can be realized as high-performance, commercially viable products there are still numerous scientific and technical challenges that must be overcome, from designing the cathode structure, to optimizing the electrolyte compositions and elucidating the complex chemical reactions that occur during charge and discharge. The scientific obstacles that are related to the performance of Li–air batteries open up an exciting opportunity for researchers from many different backgrounds to utilize their unique knowledge and skills to bridge the knowledge gaps that exist in current research projects. This review article is a summary of the most significant developments and challenges of practical Li–air batteries and the current understanding of their chemistry.     

New structures of thin air cathodes for zinc–air batteries

Thin composite cathodes for air reduction were manufactured using microfibre-based papermaking technology. The electrodes have a thin structural design, less than 0.15 mm in thickness. Composite cathode materials for oxygen reduction applications were fabricated by entrapping carbon particles in a sinter-locked network of 2–8 m diameter metal fibres. The thin structure not only results in electrodes that are 30–75% thinner than those commercially available, but also offers an opportunity for custom-built air cathodes optimized for high-rate pulse applications. Using a thin composite structure for the air cathode in a zinc–air battery that is part of a zinc–air/capacitor hybrid is likely to increase the pulse capability of the hybrid power system. The thin cathode structure provides a better, more efficient three-phase reaction zone. In a half-cell test, the ultrathin air cathode generated more than 1.0 V vs Zn/ZnO for a current of 200 mA cm^–2. Half-cell, full-cell and pulse-power tests revealed that thin composite cathodes have a better rate and pulse performance than the air cathodes commonly used.     

The synthesis of a hybrid graphene–nickel/manganese mixed oxide and its performance in lithium-ion batteries

Mixing of aqueous suspensions of delaminated NiMn layered double hydroxide (LDH) and graphene oxide leads to the instantaneous precipitation of a hybrid material that after calcination under inert atmosphere at 450 °C leads to Ni₆MnO₈ nanoparticles deposited on larger reconstituted graphene sheets. This material exhibits electrical conductivity similar to graphite, superparamagnetism and can be used as an anode for Li-ion batteries. A maximum capacity value of 1030 mA h g^?1 was found during the first discharge, and capacity values higher than 400 mA h g^?1 were still achieved after 10 cycles. The methodology used here should allow the preparation of a large variety of hybrid graphene-metal oxide materials starting from other LDHs in which the properties derived from both constituents coexist.     

The effect of Sn content on the electrocatalytic properties of Pt–Sn nanoparticles dispersed on graphene nanosheets for the methanol oxidation reaction

Direct methanol fuel cell (DMFC) electrode catalysts with improved electrochemical properties have been prepared by dispersing platinum–tin (Pt–Sn) nanoparticles onto graphene sheets. During the deposition, a majority of the oxygenated functional groups on the graphene oxide nanosheets were removed, resulting in the formation of graphene. Microstructural characterization shows that metallic Pt, Pt–Sn alloy and tin dioxide (SnO₂) nanoparticles were distributed on the graphene sheets, representing different lattice planes during the synthetic process. In terms of the electrocatalytic properties, graphene-supported Pt–Sn and graphene-supported Pt catalysts exhibited much higher current densities compared with that of commercial carbon black-supported Pt catalysts. Graphene-supported Pt–Sn increased the electrocatalytic activity, which is strongly influenced by the addition of Sn in its alloyed and oxidized forms, boosting the reaction more readily because of the lower oxidation potential.     

Experimental investigation and thermodynamic simulation of the uranium oxide–zirconium oxide–iron oxide system in air

The behavior of melts and the phase composition of crystallization products of six compositions in the uranium oxide-zirconium oxide-iron oxide system in air have been investigated. It has been revealed that crystallized samples containing 20–50 wt % uranium oxide and 25–80 wt % iron oxide (the rest is zirconium oxide) consist of five crystalline phases and involve two types of eutectic structures. The possible factors responsible for this phenomenon have been considered.     

UV light exposure of aqueous graphene oxide suspensions to promote their direct reduction,formation of graphene–metal nanoparticle hybrids and dye degradation

The use of UV light to trigger different processes involving graphene oxide sheets suspended in aqueous medium at room temperature has been investigated. These processes include (1) deoxygenation of the sheets in the absence of photocatalysts, reducing agents and stabilizers, (2) selective nucleation and growth of metal nanoparticles on the sheets to yield graphene-based hybrids and (3) decomposition of the dye molecule rhodamine B in the presence of only graphene oxide. Photoinduced heating of the suspended graphene oxide sheets by intense UV irradiation (～1 W cm^?2 delivered at the surface of the dispersion) was interpreted to generate at high temperature and reactive environment strictly localized at the sheets and their immediate aqueous medium, which in turn brings about the mentioned processes. In addition to providing a simple route toward reduction of graphene oxide dispersions, the present results suggest that intense UV light can be used to promote reactions at ambient conditions with this material that would otherwise require high temperatures, chemical reactants and/or catalysts.     

The effect of rippled graphene sheet roughness on the adhesive characteristics of a collagen–graphene system

A great amount of effort has been made in order to reach a more precise understanding of the adhesion phenomenon that happens as a vital component of several biological systems. Therefore, a firm understanding of the important factors that influence this phenomenon is of special importance in triggering the adhesive characteristics of different biological, bio-inspired and synthetic materials in fields such as tissue engineering.In this study the adhesive characteristics of a multi-material system consisting of the frequently used synthetic material, graphene, in the form of armchair-configuration sheets, and an important biological filament which is type 1 Collagen consisting of 3 alpha helices, has been studied in detail. The main emphasis of this study is placed on understanding the effects of the roughness characteristics of the inorganic elements which are the graphene sheets on the overall adhesive features of the system which are quantified within the framework of two main criteria: adhesion energy and peeling force. At first, the methodology used in order to obtain graphene sheets with various roughness values is described in detail. The abovementioned criteria are then evaluated through Molecular Dynamics (MD) modeling of the system in the NAMD simulation software environment and various simulation scenarios are studied.     

The doping of reduced graphene oxide with nitrogen and its effect on the quenching of the material’s photoluminescence

N-doped graphene (NG) was synthesized by annealing reduced graphene oxide (RGO) in an ammonia atmosphere. The dependence of the nitrogen content on the annealing temperature and the type of doping of NG were investigated. The photoluminescence (PL) properties of the RGO and NG samples were studied. The results show that RGO exhibits strong ultraviolet (UV) PL at 367 nm. The PL of RGO can be quenched by doping it with N and the quenching efficiency depends on the pyridine N content.     

Thermodynamic and kinetic studies of crystal violet dye adsorption with poly(methyl methacrylate)–graphene oxide and poly(methyl methacrylate)–graphene oxide–zinc oxide nanocomposites

We successfully prepared poly(methyl methacrylate) (PMMA)–graphene oxide (GO) and PMMA–GO–zinc oxide (ZnO) nanocomposites and characterized them using different techniques. The adsorption performances of the as-prepared composites were investigated for crystal violet (CV) dye removal. The contact time as a main factor affecting the adsorption process by adsorbents was studied. Because the adsorption capacity value for CV was found to show no extensive changes after 35 min, 35 min was selected as the best contact time for our system. The adsorption results revealed that the best capacity of CV adsorption onto the PMMA–GO and PMMA–GO–ZnO nanocomposites occurred at pH 12 and 298 K. The respective entropies (−0.208 and −0.168 kJ mol⁻¹ K⁻¹) and enthalpies (−72.86 kJ/mol, and −55.54 kJ/mol) for PMMA–GO and PMMA–GO–ZnO and Gibbs energy revealed that the process of adsorption was exothermic. In addition, the Elovich, pseudo-first-order, intraparticle diffusion, and pseudo-second-order (four types) models were applied to our kinetic study. Our results indicate that CV adsorption onto PMMA–GO and PMMA–GO–ZnO was good with the pseudo-second-order (type 1) and pseudo-first-order models because of the low χ² value and the high correlation coefficient value. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47495.     

Catalysts Ru–CeO2/Sibunit for catalytic wet air oxidation of aniline and phenol

Catalytic properties of carbon materials Sibunit (commercial samples) and ceria-promoted precious metals (Ru, Pt, Pd) supported on carbon were studied in the processes of catalytic wet air oxidation (CWAO) of aniline and phenol at elevated pressures and temperatures (T =433–473 K, P_O2 = 0.3–1.0 MPa). It was found that the activity increases when the catalyst is pretreated with hydrogen peroxide. An efficiency of Ru–CeO₂/Sibunit catalyst with a low ruthenium content (~0.6 Ru) for deep cleaning of polluted waters is demonstrated.     

Preparation and characterization of smart hydrogel nanocomposites sensitive to oxidation–reduction

Honeycomb-patterned hydrogel films sensitive to environmental oxidation–reduction supporting nanoparticle by adsorption were fabricated through the photopolymerization of ruthenium(4-vinyl-4′-methyl-2,2′-bipyridine)bis(2,2′-bipyridine)bis(hexaflurophosphate) and N-isopropylacrylamide. Nanoparticle adsorption by the hydrogel film was controlled by the dynamic changes in the surface morphology of the film in relation to environmental oxidation–reduction, which induces change of the oxidized and reduced states of ruthenium ion included in the hydrogel. For the adsorption of nanoparticles in the patterned hydrogel film, silver nanoparticles were immobilized in the hydrogel surface. Adsorptivity was obtained through measuring the released concentration of the silver nanoparticles using UV–vis spectroscopy in an aqueous solution. Desorption of Ag nanoparticles from the hydrogel surface was found to be larger in the oxidizing solution than in the reducing solution.     

Selective oxidation of hydrocarbons under air using recoverable silver ferrite–graphene (AgFeO2–G) nanocomposite: A good catalyst for green chemistry

The selective oxidation of hydrocarbons is a main academic and industrial research challenge. A lot of researches have been done about this issue, but till now relatively little attention has been paid to graphene-complex oxide nanocomposites. Herein, we report our studies on a new catalyst. Silver ferrite–graphene (AgFeO₂–G) as a separable nanocomposite from the reaction solution, was used as an effective oxidizing agent for the oxidation of various hydrocarbons (1- decene, cyclohexene, cis-cycloctene, cyclohexane, cyclooctane etc.) under mild conditions (55 ^০C, 8 h) with high conversion and selectivity using air, that is proper for ‘green’ chemistry. Metal or metal oxide nanoparticles assembled on graphene sheets revealed high electrocatalytic activity. Indeed, AgFeO₂ with graphene due to low band gap and graphene oxide with large amounts of oxygen-containing groups, provide facility catalytic activity of catalyst-supported system. We also found that, with this catalyst, selective oxidation could be achieved without the need for the addition of solvent, which is appropriate in particular for ‘green’ chemistry. The catalysts showed little deactivation and maintained their conversion and selectivity levels duration of the measurements.     

The effect of a graphite addition on oxidation of ZrB2–SiC in air at 1500 °C

Dense ZrB₂ containing 15 vol.% SiC and 15 vol.% graphite was exposed to flowing air at 1500 °C. A layered scale structure developed that consisted of (1) a uniform SiO₂-rich layer on the surface, (2) a layer of ZrO₂ and SiO₂, (3) a layer of ZrO₂ (4) a partially oxidized layer composed of porous ZrB₂, ZrO₂, and graphite, and (5) unaffected ZrB₂–SiC–C. A thermodynamic model based on volatility diagrams and consistent with the experimental observations was constructed to explain the development of the layered structure. Oxidation behavior was consistent with passive oxidation and formation of a protective surface layer. Analysis indicated that it may not be possible to form a protective surface layer without actively oxidizing SiC and producing a porous partially oxidized layer between the outer protective layer and the underlying unoxidized material.     

Effects of a graphene nanosheet conductive additive on the high-capacity lithium-excess manganese–nickel oxide cathodes of lithium-ion batteries

This study examines the effects of a graphene nanosheet (GNS) conductive additive on the performance of a highly packed (2.5 g cm^?3) lithium-ion battery cathode containing 92 wt% Li_1.1(Mn_0.6Ni_0.4)_0.9O₂ microspheres (approximately 6 μm in diameter). GNSs, approximately 2.0 nm thick and 0.5–1.0 μm in width, are introduced into an electrode slurry in the form of a dispersion in N-Methyl-2-pyrrolidone. They are substantially smaller than the oxide particles; therefore, their presence exerts no adverse influence on the packing density of the electrode. A small quantity of the GNS additive (≤200 ppm relative to the oxide mass) can significantly increase the overall electronic conductance and improve the conductance uniformity of the oxide electrode, leading to reduced polarization and enhanced specific capacity and rate performance. However, the GNS additive also promotes solid-electrolyte interphase formation, resulting in resistance buildup and capacity deterioration upon cycling. This study is the first to identify such an adverse effect caused by a graphene additive. The interplay between the positive and negative effects has led to an optimal GNS additive content of approximately 100 ppm, enhancing both the rate and cycle life performance.