Search results for "CYCLIC VOLTAMMETRY"

Experimental analysis of materials in proton exchange membrane electrolysis cells

2019

Abstract An accelerated supply and demand of energy has resulted in an increased need for efficient energy storage options, where storing energy in hydrogen gas emerges as one of the most attractive. In this study, a singular proton exchange membrane (PEM) electrolysis cell was designed using adequately low-cost materials, and tested using polarisation curves, cyclic voltammetry and AC impedance. A comparative study of various micro porous layer (MPL) materials was performed in an effort to find suitable options which are able to steadily operate under anodic conditions. The best performance was achieved using carbon cloth, however this material was unstable. Untreated porous titanium and n…

Electrochemical incineration of 1,2-dichloroethane: Effect of the electrode material

2008

The electrochemical incineration of 1,2-dichloroethane (EDC) at Pt, Au, boron-doped diamond (BDD), Ebonex, stainless steel, Ti/IrO2–Ta2O5 and PbO2 has been studied in acid media by cyclic voltammetry and bulk electrolysis. It has been shown that the performances of the process dramatically depend on the anodic material. Higher current efficiencies were obtained at BDD. In particular, at proper values of applied current density, it is possible to obtain the almost complete conversion of EDC to CO2 at BDD with current efficiencies higher than 40%.

Electrochemical reduction and carboxylation of halobenzophenones

2002

Abstract The electrochemical reduction of a series of halogenated benzophenones XC6H4COC6H4Y (1) was studied in aprotic solvents, in the absence and presence of CO2, by cyclic voltammetry (CV) and controlled-potential electrolysis. The mechanism of electroreduction in dimethylformamide (DMF) has been investigated in some detail. Most of the compounds undergo reductive carbonhalogen bond cleavage in the time window of CV. The radical anions derived from difluorobenzophenones (X=Y=4-F; X=2-F, Y=4-F) as well as from the 3-chloro derivative are quite stable with a cleavage rate constant (kc) of the order of 10−2 s−1 or less. With 4-chloro-, 2-chloro-, 4,4′-dichloro- and 2,4′-dichorobenzophen…

Unusual B4N2C2 Ligand in a Ruthenium Pseudo-Triple-Decker Sandwich Complex Displaying Three Reversible Electron-Transfer Steps

2007

Study of the electrochemical and optical properties of fullerene and methano[60]fullerenediphosphonate derivatives in solution and as self-assembled …

2014

Four methanofullerenes with phosphonate groups attached to a C60 core were synthesized to probe their electrochemical and optical properties both in solution and as self-assembled monolayer structures (SAMs). As the methano[60]fullerenediphosphonate is a water soluble derivative of the fullerene it has high potential as an imaging molecule in biological applications and in optoelectronics. For the processing of fullerene based SAMs different electrode substrates (ITO, Au and Si) with specific anchoring groups (zirconium, cysteamine and amino-silane) were used. The formation of the C60-SAMs to the surfaces were investigated by atomic force microscopy (AFM), infrared spectroscopy, contact ang…

An electrochemical quartz crystal microbalance study of lithium insertion into thin films of tungsten trioxide II. Experimental results and compariso…

1995

Abstract Lithium insertion into amorphous thin films of tungsten trioxide (a-WO 3 ) prepared by thermal vacuum evaporation of WO 3 powder has been studied experimentally by chronoamperometry, cyclic voltammetry and ac impedance spectroscopy associated with electrochemical quartz crystal microbalance (EQCM). During cathodic polarization of the electrode and at short times two antagonistic processes occur. One is a non faradaic process and is associated with the expulsion of anions from the electrode surface under the effect of the electric field built in the electrolyte when a potential difference is imposed between the electrodes. The other one is the faradaic insertion of non-solvated lith…

Electrochemical performance of activated screen printed carbon electrodes for hydrogen peroxide and phenol derivatives sensing

2019

Screen-printed carbon electrodes (SPCEs) are widely used for the electroanalysis of a plethora of organic and inorganic compounds. These devices offer unique properties to address electroanalytical chemistry challenges and can successfully compete in numerous aspects with conventional carbon-based electrodes. However, heterogeneous kinetics on SPCEs surfaces is comparatively sluggish, which is why the electrochemical activation of inks is sometimes required to improve electron transfer rates and to enhance sensing performance. In this work, SPCEs were subjected to different electrochemical activation methods and the response to H2O2 electroanalysis was used as a testing probe. Changes in to…

Electrochemistry of methylene blue at an alkanethiol modified electrode

2012

International audience; Gold surfaces were derivatized with decanethiol. The electrochemistry of methylene blue at these modified electrodes was investigated in function of the gold cleaning process and compared with the results obtained at a bare gold electrode. Cyclic voltammetry at low methylene blue concentrations (c(MB) <= 16 mu M) yielded surface behavior data. The properties of the film vary with the electrode pretreatment. Without electrochemical cleaning step, the standard potential at a gold electrode modified with 1-decanethiol is nearly the same as on a bare gold electrode. On the other hand, when the electrode is electrochemically cleaned before adsorption of the alkanethiols, …

Electrochemical response of ferrocenium filled calix[4]arene capsules in solution and immobilized on gold

2008

Abstract Hydrogen-bonded dimers of tetra-urea calix[4]arenes are able to include ferrocenium ions as a guest. Heterodimeric capsules are exclusively formed in 1:1 mixtures of tetra-arylurea calix[4]arene 1 with tetra-tosylurea calix[4]arene 2. Sulfide groups attached via spacers on the urea rim of 1 allow their binding to metal surfaces rendering simultaneously their dissociation more difficult. Thus, the electrochemical response of encapsulated ferrocenium could be studied in a self-assembled monolayer (SAM) in addition to the solution electrochemistry with cyclic voltammetry. The stability of the electrochemically active monolayers was tested after a heat treatment (225 °C for 30 min in N…

Measured and Calculated Oxidation Potentials of 1-X-12-Y-CB11Me10– Anions

2012

Cyclic voltammetry of 31 icosahedral carborane anions 1-X-12-Y-CB(11)Me(10)(-) at a Pt electrode in liquid SO(2) revealed a completely reversible one-electron oxidation even at low scan rates, except for the anions with Y = I, which are oxidized irreversibly up to a scan rate of 5.0 V/s, and the anion with X = COOH and Y = H, whose oxidation is irreversible at scan rates below 1.0 V/s. Relative reversible oxidation potentials agree well with RI-B3LYP/TZVPP,COSMO and significantly less well with RI-BP86/TZVPP,COSMO or RI-HF/TZVPP,COSMO calculated adiabatic electron detachment energies. Correlations with HOMO energies of the anions are nearly as good, even though the oxidized forms are subjec…