Search results for " electrode"
showing 10 items of 301 documents
Unified Rate Theory of Electrochemistry and Electrocatalysis: Fixed Potential Formulation for General, Electron Transfer, and Proton-Coupled Electron…
2019
Atomistic modeling of electrocatalytic reactions is most naturally conducted within the grand canonical ensemble (GCE) which enables fixed chemical potential calculations. While GCE has been widely adopted for modeling electrochemical and electrocatalytic thermodynamics, the electrochemical reaction rate theory within GCE is lacking. Molecular and condensed phase rate theories are formulated within microcanonical and canonical ensembles, respectively, but electrocatalytic systems described within the GCE require extension of the conventionally used rate theories for computation reaction rates at fixed electrode potentials. In this work, rate theories from (micro)canonical ensemble are gener…
STUDY OF CAPACITIVE ELECTRODES FOR REVERSE ELECTRODIALYSIS PROCESSES
2018
It has been calculated that the energy dissipated wherever the rivers get to the sea this corresponds to an amount of about 2 TW of power [1]. Recovering part of this energy could attenuate the dependency of our economic system from fossil fuels. The techniques conceived to exploit this blue energy are grouped within the family of the salinity gradient technologies, where pressure-retarded osmosis (PRO) and reverse electrodialysis (RED) are regarded as the most established technologies [2]. Nevertheless, their power is limited respectively by various factors including the kinetics of electrodes reactions. Conversely, the use of capacitive electrodes proposed by Brogioli in 2009, does not se…
Sensor Properties of Pristine and Functionalized Carbon Nanohorns
2016
Nanodispersions of pristine single-wall carbon nanohorns (i.e., p-SWCNHs) and oxidized-SWCNHs (i.e.; o-SWCNHs) were used to modify screen printed electrode (SPE). p-SWCNHs and o-SWCNHs were fully characterized by using several analytical techniques, as: HR-TEM (High Resolution-Transmission Electron Microscopy), FE-SEM/EDX (Field Emission-Scanning Electron Microscopy/Energy Dispersive X-ray Analysis), Raman spectroscopy, thermogravimetric analysis, differential thermal analysis (DTA), and the Brunauer-Emmett-Teller (BET) method. The chemically modified SPEs were also characterized with Cyclic Voltammetry (CV), using several different electro-active targets. In all cases, p-SWCNHs showed bett…
Properties of amphiphilic terminally substituted conjugated nonaene- and 2-docosylnonaene carboxylic acids in monolayers at the air-water interface
1991
was a lo-' M Co(NO,), + lo-' M CH,COONa solution, with pH 7.5; the counter electrode was a Pt sheet, conveniently located in the electrochemical cell. After deposition, the electrochemical/electrochromic properties of the films were analyzed in degassed lo-' M KOH electrolyte, in a three electrode cell (Pt wire counter electrode, saturated calomel reference electrode) with optical windows. A PAR 173 potentiostat-galvanostat associated with a PAR 175 function generator was used in the electrochemical experiments. Data were recorded in a analogical X-Y (X-T) recorder. Monochromatic transmission (He-Ne laser, A = 632.8 nm) was recorded in situ, by means of a versatile optical bench; spectral t…
Proton exchange membrane fuel cell made of magnetron sputtered Pt–CeO and Pt–Co thin film catalysts
2015
Abstract Preparation of catalysts for proton exchange membrane fuel cells (PEMFCs) is of growing interest during last years. The magnetron sputtering technique is a promising method of catalyst preparation because it permits to synthesize catalysts in a fast and relatively less expensive way, however control of specific surface and durability of such catalysts still remains the main concern. We tested a single cell PEMFC catalyzed by using exclusively thin film approach by combining state-of-the art Pt-doped cerium oxide anode and a new Pt–Co alloy cathode. We have shown that beside very high mass activity of the catalysts relative to the membrane electrode assembly the catalyst nanoporous …
Speciation of Al3+ in fairly concentrated solutions (20 to 200 mmol L-1) at I = 1 mol L-1 (NaNO3), in the acidic pH range, at different temperatures.
2011
AbstractThe hydrolysis of Al3+ was studied in aqueous 1 mol L−1 NaNO3 solution at different concentrations (20–200 mmol L−1) and temperatures (283.15–343.15 K) by potentiometry (ISE-H+, glass electrode). Many different speciation models were considered in the calculations and it was found that the best model is represented by the following species: Al(OH)2+, Al(OH)45+, Al13(OH)327+. Hydrolysis constants and enthalpy changes at different temperatures are reported.
Evidence of intramolecular electron transfer between two metallic atoms in a bimetallic complex by electrochemical methods
2005
The electrochemical properties of the monomeric complex [(η5-C5H5)(μ-η5:η1-C5H4(CH2)2P(C6H5)2TiCl2] 1 and the heterobimetallic complex [(η5-C5H5)(μ-η5:η1-C5H4(CH2)2P(C6H5)2TiCl2][RuCl2(C6H4(CH3)(C3H7))] 2 have been studied by cyclic voltammetry, controlled potential electrolysis and rotating disk electrode voltammetry. An unexpected electron transfer between the two heterobimetallic atoms has been observed. This transfer takes place via an intramolecular interaction, hence via a chloride bridge. Electrochemical simulation has been carried out to verify experimental results and to obtain the kinetic constant of the proposed square scheme.
Substituent effect on the redox potential of substituted (aryl)(2-nitrobenzo[ b ]thiophen-3-yl)amines
2001
Abstract The electronic effect of some meta- or para-substituents on the reduction of the title compounds has been investigated. The reversible reduction potential values of these compounds have been evaluated by cyclic voltammetry at a mercury electrode in 0.1 M tetraethylammoniumtetrafluoroborate, dimethylsulfoxide solutions. The substituent effect depends on both its nature and its position. The reduction potential values of the derivatives studied have been correlated with the Hammett substituent constants.
Convective mass transfer to partially recessed and porous electrodes
2003
Abstract The diffusional problem of a rotating porous electrode has been analysed based on the mass transfer equations for a partially blocked electrode. It is shown that the porous geometry leads to a dependence of the current on rotation rate identical to that corresponding to a coupled diffusion-activated electron transfer mechanism. The apparent rate constant, however, is related only to the geometry of the porous surface. It is shown that the characteristic diffusional length corresponds to the pore dimension modified by a term including the transition from linear to spherical diffusional geometry at the pore entrance. The theory is compared with experimental results for the reduction …
Electrochemical behaviour of poly(neutral red) on an ITO electrode
1998
Abstract The formation of a radical cation, by electrochemical oxidation of the neutral red dye in acidic aqueous solution, is controlled by diffusion towards the electrode surface. This is the initiation step of the electrogeneration, potentiostatic or potentiodynamic, of poly(neutral red) films on an indium–tin oxide (ITO) electrode. The polymeric film is a redox semi-conductor, and shows a microporous membrane-like character. Its electrochemical behaviour depends on the generation process. The hydrogen ions play a double role: first as reactants at electrochemical and acid–base equilibrium, second as counterions of the electrons. The global process of the electron-hopping is limited by t…