One-pot synthesis of ultrasmall PtAg nanoparticles decorated on graphene as a high-performance catalyst toward methanol oxidation

A one-pot synthesis method is utilized for the fabrication of ultrasmall platinum-silver nanoparticles decorated on graphene (PtAg/G) catalyst. This method has several advantages such as inexpensiveness, simplicity, low temperature, surfactant free, reductant free, being environmentally friendly and greenness. In this work, graphene and silver formate were dispersed in ultrapure water in an ultrasonic bath at 25 °C followed by through a galvanic displacement reaction; to prepare PtAg/G, PtCl₂ was added to the suspension under mild stirring condition. The morphology, crystal structure and chemical compositions of the as-fabricated PtAg/G and Pt/C catalysts were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD) and Energy dispersive X-ray spectroscopy (EDS) techniques. Electrochemical techniques, including cyclic voltammetry (CV) and chronoamperometry (CA) measurements were used to analyze the electrochemical activity of the PtAg/G and Pt/C catalysts. The TEM images illustrate the uniform distribution of ultrasmall PtAg nanoparticles with the average size of 2–3 nm on the graphene nanosheets. The PtAg/G promoted the current density 2.46 times as much as Pt/C with a negative shift in onset oxidation potential and peak potential for oxidation reaction of methanol. Besides, the novel PtAg/G catalyst shows large electrochemically active surface area, lower apparent activation energy, and higher levels of durability in comparison to the Pt/C catalyst for the oxidation of methanol. The PtAg/G catalyst depicts extraordinary catalytic performance and stability to those of the Pt/C catalyst toward methanol oxidation in alkaline media.     

Cross-linked poly(N-alkyl-4-vinylpyridinium) iodides as new eco-friendly inhibitors for corrosion study of St-37 steel in 1 M H2SO4

Iranian Polymer Journal - Cross-linked poly (N-alkyl-4-vinylpyridinium) iodides abbreviated as P4-VPMI, P4-VPOI and P4-VPDI, were synthesized from quaternization of poly(4-vinyl pyridine)...     

Novel fabrication of PdCu nanostructures decorated on graphene as excellent electrocatalyst toward ethanol oxidation

In this study, the electrochemical reduction reaction of copper(II) formate on the graphene/glassy carbon electrode (G/GCE) surface in the HCl (5 wt.%) was employed for fabrication of the PdCu nanostructures by galvanic displacement reaction. This method has a number of advantages including being environmentally-friendly, simplicity, inexpensiveness and fast. The PdCu nanostructures decorated on the G/GCE were fabricated in two steps: (1) electrochemical reduction reaction of copper(II) formate to Cu on the G/GCE and (2) the galvanic replacement reaction between Cu and Pd²⁺ ions. The physical and electrochemical properties of as-prepared PdCu/G were investigated via Field Emission Scanning Electron Microscopy, Energy Dispersive X-ray Spectroscopy, Cyclic Voltammetry, Chronoamperometry, and Electrochemical Impedance Spectroscopy. The PdCu/G compositional effect on ethanol oxidation in alkaline media is investigated. The results were shown that the catalytic activity and durability of PdCu/G catalyst are superior to those of Pd/C electrocatalyst for ethanol oxidation. The PdCu/G increased the current density 6.2 times more than Pd/C with a 50 mv negative shift in onset potential for electrooxidation of ethanol. Besides, the novel PdCu/G catalyst exhibits large electrochemically active surface area, lower apparent activation energy, higher levels of stability, poisoning tolerance, and lower charge transfer resistance compared to the Pd/C for the oxidation of ethanol.     

Inhibition of aluminum corrosion in acid solution by environmentally friendly antibacterial corrosion inhibitors: Experimental and theoretical investigations

Protection of Metals and Physical Chemistry of Surfaces - The inhibition performance of penicillin G(I), methicillin(II) and nafcillin(III) on the corrosion of aluminum in a 1 M HCl solution has...     

Platinum nanoparticles self-assembled onto chitosan membrane as anode for direct methanol fuel cell

In this article, incorporation of platinum nanoparticles (PtNPs) into chitosan-coated glassy carbon (GC) electrode for methanol oxidation is studied. Pt–chitosan nanocomposites are prepared and characterized by UV–vis spectroscopy, X-ray powder diffraction (XRD), and transmission electron microscopy (TEM). Catalytic activity of GC–PtNPs–chitosan electrode for the electrooxidation of methanol is studied by cyclic voltammetry and chronoamperometry. The current density and potential of the methanol oxidation are affected by amount of platinum, methanol, sulfuric acid, and chitosan. The current density of the methanol oxidation at GC–PtNPs–chitosan electrode is measured in optimized conditions and compared with that obtained at the glassy carbon modified electrode by Pt with different polymers.     

A simple and fast method for the preparation of super active Pd/CNTs catalyst toward ethanol electrooxidation

For the first time, galvanic reduction by zinc sheet is used as a new strategy to prepare modified electrodes. In this work, glassy carbon electrode (GCE) was modified by decoration of Pd nanostructures on carbon nanotubes (Pd/CNTs). In this method, deposited PdCl₂ on CNTs was directly reduced to metallic Pd nanostructure using a zinc sheet in HCl (2% w/w) solution. This approach offers a number of advantages including being very fast, simple and green; and modified electrodes show high activity. The prepared catalyst is characterized by Field Emission Scanning Electron Microscopy, X-Ray Diffraction and energy-dispersive X-ray and Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES). In addition, electrochemical measurements show that the performance as well as the stability of the as-prepared catalyst for ethanol oxidation is outstanding. The Pd/CNTs catalyst shows higher mass current density, which is 7.9 times as high as that of commercial Pd/C.