Aluminum nanotubes as an efficient catalyst for hydrogen production via thermochemical water splitting: a reactive molecular dynamics simulation.

Water splitting is the process of using energy to break down water molecules into hydrogen and oxygen. The use of an aluminum catalyst in the thermochemical process can help to increase the efficiency and rate of the reaction. Furthermore, aluminum is a relatively inexpensive material that can be easily produced, making it an appealing option for use in large-scale water-splitting operations. We investigated the reaction mechanism between aluminum nanotubes and water at various temperatures using reactive molecular dynamic simulations. We found that an aluminum catalyst makes it possible to split water at temperatures higher than T > 600 K. It was also observed that the yield of H2 evolution is dependent on the diameter of the Al nanotube and decreases with increasing size. During the process of splitting water, the inner surfaces of the aluminum nanotubes are seen to be severely eroded, as shown by changes in the aspect ratio and solvent-accessible surface area. In order to compare the H2 evolution efficiency of water with other solvents, we also split a variety of solvents, including methanol, ethanol, and formic acid. We presume that our study will give researchers enough knowledge to create hydrogen through thermochemical process in the presence of an aluminum catalyst by dissociating water and other solvent molecules.

Efficient anti-corrosive coating of cold-rolled steel in a seawater environment using an oil-based graphene oxide ink.

We report the production of an efficient anti-corrosive coating of cold-rolled (CR) steel in a seawater environment (∼3.5 wt% NaCl aqueous solution) using an oil-based graphene oxide ink. The graphene oxide was produced by heating Aeschynomene aspera plant as a carbon source at 1600 °C in an argon atmosphere. The ink was prepared by cup-milling the mixture of graphene oxide and sunflower oil for 10 min. The coating of ink on the CR steel was made using the dip-coating method, followed by curing at 350 °C for 10 min in air atmosphere. The results of the potentiodynamic polarization show that the corrosion rate of bare CR steel decreases nearly 10,000-fold by the ink coating. Furthermore, the salt spray test results show that the red rusting in the ink-coated CR steel is initiated after 100 h, in contrast to 24 h and 6 h in the case of oil-coated and bare CR steel, respectively. The significant decrease in the corrosion rate by the ink-coating is discussed based on the impermeability of graphene oxide to the corrosive ions.

Observation of large positive magneto-resistance in bubble decorated graphene oxide films derived from shellac biopolymer: a new carbon source and facile method for morphology-controlled properties.

We report a large positive magneto-resistance (MR) in bubble decorated graphene oxide films that are derived from shellac biopolymer as a carbon source. These films were produced on a quartz substrate by heating the biopolymer coated substrate at 900 °C in an argon atmosphere. The characterization data of the films using Raman, X-ray photoelectron spectroscopy, field emission scanning electron microscopy and transmission electron microscopy reveal that shellac can be used as a new carbon source to produce transparent bubble decorated graphene oxide films. The magneto-resistance results show a 130% change in the resistance of the films at 3 K under a perpendicular magnetic field of 15 T, and the value decreases exponentially up to 50 K. The observed MR properties of the bubble decorated graphene oxide films are explained using a weak anti-localization and quantum interference model in the low magnetic field region, while the Lorentz force accounts for the MR properties well in the high magnetic field region.

Pt-Pd alloy nanoparticle-decorated carbon nanotubes: a durable and methanol tolerant oxygen reduction electrocatalyst.

We describe the decoration of multiwalled carbon nanotubes (MCNTs) with Pt-Pd alloy nanoelectrocatalysts of three different compositions and their electrocatalytic performance toward the oxygen reduction reaction (ORR). The decoration of the MCNTs involves polymer-assisted impregnation of metal precursors PtCl(6)(2-) and PdCl(6)(2-) and the subsequent reduction of the impregnated precursors by a modified polyol route. The composition of the catalyst was controlled by tuning the molar ratio of the precursors during their impregnation. Electron probe microscopic analysis shows that the catalysts have compositions of Pt(46)Pd(54,) Pt(64)Pd(36) and Pt(28)Pd(72). The Pt(46)Pd(54) and Pt(64)Pd(36) catalysts have truncated octahedral and icosahedral shapes with a size ranging from 8 to 10 nm. On the other hand, the catalyst of Pt(28)Pd(72) composition has a spherical/quasispherical shape with a size distribution of 1-2 nm. The XPS measurement confirms the signature of metallic Pt and Pd. The Pt(46)Pd(54) catalyst has a pronounced electrocatalytic activity toward the ORR with a specific and mass activity of 378 µA cm(Pt-Pd)(-2) and 64 µA µg(Pt-Pd)(-1), respectively at 0.8 V. Moreover, the Pt(46)Pd(54) nanoelectrocatalyst is highly durable and it retains its initial catalytic activity even after 1000 extensive cycles. Interestingly, this catalyst has a very high tolerance toward methanol and it does not favor the oxidation of methanol in the potential window of 0.1-1.4 V. The electrocatalytic activity of the alloy electrocatalyst is compared with commercially available Pt black and MCNT-supported spherical Pt nanoparticles. The catalytic activity of the Pt(46)Pd(54) nanoelectrocatalyst is higher than the other catalysts. The Pt(46)Pd(54) catalyst outperforms the electrocatalytic activity of all other catalysts.

A rapid room temperature chemical route for the synthesis of graphene: metal-mediated reduction of graphene oxide.

A rapid and facile route for the synthesis of reduced graphene oxide sheets (rGOs) at room temperature by the chemical reduction of graphene oxide using Zn/acid in aqueous solution is demonstrated.

Stabilization of intrinsic defects at high temperatures in ZnO nanoparticles by Ag modification.

The stabilization of defects in ZnO at high temperatures has been investigated. The properties of unmodified and modified ZnO nanoparticles (NPs) with 2 at.% of Ag prepared by microwave assisted combustion method, have been systematically studied using X-ray diffraction (XRD), photoluminescence (PL), X-ray photoelectron spectroscopy (XPS) and photocatalytic activity measurements. Though the XRD data shows a marginal shift in the ZnO peak position upon Ag addition, the amount of shift does not change with annealing temperatures. The PL data reveals that the defect mediated visible emission intensity of unmodified ZnO NPs increases with increase in the annealing temperature, whereas it remains almost unchanged in Ag-ZnO. This study clearly establishes that silver is an efficient stabilizer of intrinsic defects in ZnO at high temperatures. This is further supported by the core and valence band XPS spectra.

A facile approach for morphosynthesis of Pd nanoelectrocatalysts.

A facile approach has been developed for synthesis of highly-structured, anisotropic Pd nanostructures. The dendritic Pd nanostructures show superior performance toward oxidation of formic acid and methanol for fuel cell application.

Effect of Ru-Mn redox interactions on the hole carrier density in pulsed electron deposited La(1-x)Pb(x)Mn(0.8)Ru(0.2)O(3) (0.2≤x≤0.4) thin films.

Pulsed electron deposited thin films of Ru substituted La(1-x)Pb(x)Mn(0.8)Ru(0.2)O(3) (0.2≤x≤0.4) show an increase in the magneto-resistance ratio by ∼5-15% at the respective metal to insulator transition (T(MIT)) temperature when compared to the parent La(0.6)Pb(0.4)MnO(3) thin film. A systematic decrease in T(MIT) is observed from ∼310 to ∼260 K when the hole (Pb) concentration varies from 40 to 20% with constant 20% Ru substitution at the Mn site. The x-ray rocking curve and high-resolution transmission electron microscopy (HRTEM) images of the thin films suggest that Ru occupies the Mn site and shows epitaxial growth of the films on the LaAlO(3) (LAO) substrate. Transport and magneto-resistive properties show that Ru substitution maintains a considerable hole carrier density (due to Mn(4+):t(2g)(3)e(g)(0)/Ru(5+):t(2g)(3)e(g)(0)) even for La(0.8)Pb(0.2)Mn(0.8)Ru(0.2)O(3) (8282) composition, which influences the double exchange interactions.

Evidence for an anomalous redox ionic pair between Ru and Mn in SrRu0.5Mn0.5O3: an X-ray absorption spectroscopy approach.

X-ray absorption spectroscopy studies of the polycrystalline SrRu0.5Mn0.5O3 have been performed at Ru, Mn-L2,3 edges. The 2p-->t2g related peak at the Ru-L2 edge is more intense than the Ru-L3 edge and a shift of the 2p-->eg related peak by approximately 0.8 eV to higher energy than that of the Ru(IV) compound, SrRuO3 is observed. In combination with a crystal field multiplet calculation approach, a possible anomalous change in the spectral features is explained based on the existence of a redox ionic pair involving Ru(IV)/Ru(v)<-->Mn(III)/Mn(IV).