Electrodeposition of Nickel onto 12K Carbon Fibre Tow in a Continuous Manner

Nickel-coated carbon fibre (NiCCF) is an important composite material, which finds nu- merous engineering applications, primarily within: computer, telecommunication, automotive and military industries. In general, NiCCF can be produced by one of the three methods, namely: chemical vapour deposition (CVD), electroless, and electrochemical (galvanic) deposition of Ni on a carbon fibre tow material. The present paper reports a study of the process of nickel electrodeposition (at ultrathin layers of ≈ 0.3–0.5 μm) onto the surface of 12K (12000 single filaments) carbon fibre (CF) tow, carried-out in a continuous way. In addition, the effect of selected pre-treatments applied to carbon fibre, as well as that of operational parameters of the process, on the quality of the NiCCF product were investigated. (doi: 10.5562/cca1743

The Process of Electrooxidation of Quercetin 3,4\u27-di-O-β-Glucopyranoside at Glassy Carbon Electrode

The present paper reports electrochemical and UV-VIS spectroscopic studies on the process of electrooxidation of quercetin 3,4\u27-di-O-β-glucopyranoside (Q 3,4\u27-diglc) molecule, at glassy carbon electrode surface in 0.1 M sodium acetate – acetic acid buffer in 90 % methanol solution. The process starts at 3\u27-OH group (ring B), followed by oxidation of 5,7-dihydroxyl group in ring A. As a result of electrochemical reactions, the surface area of glassy carbon (GC) electrode becomes extensively blocked by Q 3,4\u27-diglc oxidation products

Dithiooxamide Modified Glassy Carbon Electrode for the Studies of Non-Aqueous Media: Electrochemical Behaviors of Quercetin on the Electrode Surface

Electrochemical oxidation of quercetin, as an important biological molecule, has been studied in non-aqueous media using cyclic voltammetry, electrochemical impedance spectroscopy and scanning electron microscopy. To investigate the electrochemical properties of quercetin, an important flavonoid derivative, on a different surface, a new glassy carbon electrode has been developed using dithiooxamide as modifier in non-aqueous media. The surface modification of glassy carbon electrode has been performed within the 0.0 mV and +800 mV potential range with 20 cycles using 1 mM dithioxamide solution in acetonitrile. However, the modification of quercetin to both bare glassy carbon and dithiooxamide modified glassy carbon electrode surface was carried out in a wide +300 mV and +2,800 mV potential range with 10 cycles. Following the modification process, cyclic voltammetry has been used for the surface characterization in aqueous and non-aqueous media whereas electrochemical impedance spectroscopy has been used in aqueous media. Scanning electron microscopy has also been used to support the surface analysis. The obtained data from the characterization and modification studies of dithioxamide modified and quercetin grafted glassy carbon electrode showed that the developed electrode can be used for the quantitative determination of quercetin and antioxidant capacity determination as a chemical sensor electrode

Assessment of the roughness factor effect and the intrinsic catalytic activity for hydrogen evolution reaction on Ni-based electrodeposits

The hydrogen evolution reaction (HER) was studied in 30 wt.% KOH solution at temperatures ranging between 30 and 80 °C on three type of electrodes: (i) rough pure Ni electrodeposits, obtained by applying a large current density; (ii) smooth NiCo electrodeposits; (iii) smooth commercial Ni electrodes. By using steady-state polarization curves and electrochemical impedance spectroscopy (EIS) the surface roughness factor and the intrinsic activities of the catalytic layers were determined. These techniques also permitted us to determine the mechanism and kinetics of the HER on the investigated catalysts. Different AC models were tested and the appropriate one was selected. The overall experimental data indicated that the rough/porous Ni electrode yields the highest electrocatalytic activity in the HER. Nevertheless, when the effect of the surface roughness was taken into consideration, it was demonstrated that alloying Ni with Co results in an increased electrocatalytic activity in the HER when comparing to pure Ni. This is due to an improved intrinsic activity of the material, which was explained on the basis of the synergism among the catalytic properties of Ni (low hydrogen overpotential) and of Co (high hydrogen adsorption).Isaac Herraiz-Cardona is grateful to the Ministerio de Ciencia e Innovacion (Spain) for a postgraduate grant (Ref. AP2007-03737). This work was supported by Generalitat Valenciana (Project PROMETEO/2010/023)Herraiz Cardona, I.; Ortega Navarro, EM.; Garcia-Anton, J.; Pérez-Herranz, V. (2011). Assessment of the roughness factor effect and the intrinsic catalytic activity for hydrogen evolution reaction on Ni-based electrodeposits. International Journal of Hydrogen Energy. 36(16):9428-9438. https://doi.org/10.1016/j.ijhydene.2011.05.047S94289438361

Enhancement of electrochemical activity of Raney-type NiZn coatings by modifying with PtRu binary deposits: Application for alkaline water electrolysis

This study presents electrochemical preparation and characterization of PtRu-modified Cu/Ni/NiZn electrodes (Cu/Ni/NiZn-PtRu) as cathode materials for alkaline water electrolysis. The electrodes were characterized using energy dispersive X-ray spectroscopy (EDX), scanning electron microscopy (SEM) and X-ray diffraction (XRD) techniques. Their electrochemical activities as cathode materials for alkaline water electrolysis were evaluated with the help of current potential curves. The results showed that the PtRu-modified layers have porous structures with relatively low Pt and Ru chemical compositions. The modification of the alkaline leached Cu/Ni/NiZn surface by Pt and/or Ru enhances the electrochemical activity of the electrode. Their catalytic activity depends on the molar ratios of Pt and Ru; the PtRu binary deposit with the percentage weight ratio of approximately 56:44 exhibits the highest hydrogen evolution activity among the studied electrodes. The enhanced hydrogen evolution activity of the PtRu-modified electrodes was related to the porous surface and/or a possible synergistic effect between the metals. Copyright (c) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved

Ethanol Oxidation on Pt Single-Crystal Electrodes: Surface-Structure Effects in Alkaline Medium

Ethanol oxidation in 0.1 M NaOH on single-crystal electrodes has been studied using electrochemical and FTIR techniques. The results show that the activity order is the opposite of that found in acidic solutions. The Pt(111) electrode displays the highest currents and also the highest onset potential of all the electrodes. The onset potential for the oxidation of ethanol is linked to the adsorption of OH on the electrode surface. However, small (or even negligible) amounts of COads and carbonate are detected by FTIR, which implies that cleavage of the C[BOND]C bond is not favored in this medium. The activity of the electrodes diminishes quickly upon cycling. The diminution of the activity is proportional to the measured currents and is linked to the formation and polymerization of acetaldehyde, which adsorbs onto the electrode surface and prevents further oxidation.This work has been financially supported by the MCINN-FEDER (Spain) and Generalitat Valenciana through projects CTQ 2010-16271 and PROMETEO/2009/045 respectively

Electrocatalytic urea mineralization in aqueous alkaline medium using NiIIcyclam-modified nanoparticulate TiO2 anodes and its relationship with the simultaneous electrogeneration of H2 on Pt counterelectrodes

NiIIcyclam-modified nanoparticulate TiO2-coated ITO electrodes (ITO/TiO2//NiIIcyclam) were prepared by electropolymerization of NiIIcyclam monomers to TiO2-coated ITO electrodes (ITO/TiO2) to improve electrocatalytic urea CO(NH2)2 oxidation in alkaline aqueous solutions. A high value adding secondary effect was the collection of electrons at Pt cathodes, to simultaneously generate H2 from water reduction. NiIIcyclam-modified ITO electrodes (ITO//NiIIcyclam) were also prepared by electropolymerization of NiIIcyclam monomers to bare ITO electrodes (ITO) for comparison purposes. In the presence of the TiO2 nanoparticles, the urea mineralization on NiIIcyclam coatings was doubled (23.95% – organic carbon removal at 120 min of electrolysis) compared to those without TiO2 nanoparticles (13.02% – organic carbon removal at 120 min of electrolysis). In agreement, the faradaic efficiency for H2 generation at the Pt cathode, electrically connected to an anode having TiO2 nanoparticles (0.99 at 120 min of electrolysis), was also twice as effective than that observed when the same Pt cathode was electrically connected to an anode without TiO2 nanoparticles (0.46 at 120 min of electrolysis). The experimental results indicated that the poisoning of NiII centers (which is caused by an excessive production of CO intermediates during the urea oxidation on both NiIIcyclam-modified anodes) was strongly inhibited in the presence of the nanoparticulate TiO2|NiIIcyclam junction. A final comparison between our results and those reported in selected publications revealed that the NiIIcyclam-modified nanoparticulate TiO2-coated ITO anodes here developed, constitutes a promising electrocatalytic system for performing direct urea mineralization at a relative short electrolysis time. Furthermore, the combination of the following phenomena: (a) effective charge separation on the semiconducting ITO|nanoparticulate TiO2 junctions, (b) remarkable capabilities of the nanoporous TiO2 films for tuning the load of OH� anions demanded by the urea oxidation and, (c) outstanding capabilities of the TiO2 nanoparticles for capturing CO intermediates (at Ti3+ donor sites), successfully promoted the enhancement of the electron external transport to Pt cathodes, and consequently improved the faradaic efficiency associated to the cathodic generation of H2

Fuel cells - the future of electricity generation for portable applications

Fossil fuels, including crude oil, coal and natural gas are currently the key resources for world energy supply. Hence, the majority of electrical energy production is realized via combustion of conventional fuels, such as: coal, methane and petroleum. However, increasing emissions of pollutants and greenhouse gases from fossil fuel-based electricity production (especially withrespect to SO2, NOx and CO2 discharge) bring about major environmental concerns. In addition, the status of conventional (fossil) fuel reserves is still uncertain. Thus, production of "clean" electrical energy, especially from renewable resources, such as: biomass, solar, photovoltaic, geothermal, hydro and wind energy sources becomes of significant importance to the world's economy. Fuel cells (FCs) are electrochemical cells, which convert a source fuel (e.g. H2, CH4, alcohols, etc.) into an electric current. They generate electricity inside a cell via electrochemical reactions between a fuel and an oxidant, in the presence of an electrolyte. In general, most of fuel cells can be operated as emission-free devices, based on fuels produced fromrenewable resources. With a variety of possible FC types, fuel cells could potentially serve in stationary, transportation or portable applications. This work is a review of the state-of-the-art in fuel cell technology, with respect to FC employment in portable applications

An Innovative 500 W Alkaline Water Electrolyser System for the Production of Ultra-Pure Hydrogen and Oxygen Gases

This paper communicates on an innovative, laboratory size alkaline water electrolyser (AWE) system, capable of efficiently producing ultra-pure hydrogen and oxygen gases. The system is composed of a zero-gap, bipolar-electrode stack, equipped with a polymer-based membrane, along with two drying columns for effective purification of H2 and O2 gaseous products. An optimal electrochemical efficiency of the electrolyser stack is provided through the employment of catalytically activated, extended surface-area nickel foam electrodes. Laboratory electrochemical examinations of the electrolyser included a series of galvanostatic AWE and alternating current (a.c.) impedance (single cell) experiments. Complementary examinations covered catalyst’s surface topography analysis by combined SEM (Scanning Electron Microscopy) and EDX (Energy Dispersive X-ray Spectroscopy) techniques along with chromatographic evaluation of the purity of hydrogen and oxygen products