Search results for "Electrode potential"

showing 10 items of 36 documents

Polypyrrole films functionalized with pendant titanocene dichloride complexes: Ellipsometric study of the electropolymerization process

2007

Electrochemical and ellipsometric methods have been used to study the electropolymerization process of a functionalized monomer, Tc3Py (in which pyrrole is covalently bonded with titanocene dichloride complex) on platinum electrode from a dilute monomer solution in acetonitrile. The deposition has been performed in the potentiodynamic regime. A new method for the acquisition and treatment of ellipsometric data has been proposed which allowed us to analyze the evolution of the film properties at each potential. The model of a single uniform layer was unable to describe the ellipsometric experimental observations with the necessary precision. A proper fitting of the data has been achieved con…

Absorbancechemistry.chemical_compoundMonomerchemistryAbsorption spectroscopyEllipsometryGeneral Chemical EngineeringElectrodeElectrochemistryAnalytical chemistryMolar absorptivityPolypyrroleElectrode potentialElectrochimica Acta
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Physicochemical characterization of passive films on niobium by admittance and electrochemical impedance spectroscopy studies

2005

An analysis of the electronic properties of amorphous semiconductor-electrolyte junction is reported for thin (D ox < 20 nm) passive film grown on Nb in acidic electrolyte. It will be shown that the theory of amorphous semiconductor-electrolyte junction (a-SC/EI) both in the low band-bending and high band-bending regime is able to explain the admittance data of a-Nb 2 O 5 /El interface in a large range (10 Hz-10 kHz) of frequency and electrode potential values. A modelling of experimental EIS data at different potentials and in the frequency range of 0.1 Hz-100 kHz is presented based on the theory of amorphous semiconductor and compared with the results of the fitting of the admittance data…

AdmittanceChemistryGeneral Chemical EngineeringNiobiumAnalytical chemistrychemistry.chemical_elementphysicochemical characterization; semiconductor-electrolyte junction; electrochemical impedance spectroscopyElectrolyteAmorphous solidDielectric spectroscopysemiconductor-electrolyte junctionelectrochemical impedance spectroscopySettore ING-IND/23 - Chimica Fisica Applicataphysicochemical characterizationElectrochemistryDensity of statesElectrical impedanceElectrode potential
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Protection by extra virgin olive oil against oxidative stress in vitro and in vivo. Chemical and biological studies on the health benefits due to a m…

2017

Abstract We report the results of in vivo studies in Caenorhabditis elegans nematodes in which addition of extra virgin olive oil (EVOO) to their diet significantly increased their life span with respect to the control group. Furthermore, when nematodes were exposed to the pesticide paraquat, they started to die after two days, but after the addition of EVOO to their diet, both survival percentage and lifespans of paraquat-exposed nematodes increased. Since paraquat is associated with superoxide radical production, a test for scavenging this radical was performed using cyclovoltammetry and the EVOO efficiently scavenged the superoxide. Thus, a linear correlation (y = -0.0838x +19.73, regres…

Animals; Caenorhabditis elegans; Cell Cycle; Cell Line; Electron Spin Resonance Spectroscopy; Humans; In Vitro Techniques; Olive Oil; Oxidative Stress; Paraquat; Rats; Reactive Oxygen Species; Diet Mediterranean0301 basic medicineAntioxidantmedicine.medical_treatmentlcsh:MedicineMediterraneanmedicine.disease_causeDiet MediterraneanBiochemistryAntioxidantsMonocytesMyoblastschemistry.chemical_compoundWhite Blood Cells0302 clinical medicineParaquatGalvinoxylSuperoxidesAnimal CellsPlant ProductsMedicine and Health SciencesElectrochemistryFood sciencelcsh:Sciencechemistry.chemical_classificationMultidisciplinarySuperoxideStem CellsCell CycleAgricultureOxidesLipidsPeroxidesHydroperoxideChemistry030220 oncology & carcinogenesisPhysical SciencesCellular TypesResearch ArticleParaquatImmune CellsImmunologyIn Vitro TechniquesSettore BIO/09Vegetable OilsCell Line03 medical and health sciencesmedicineAnimalsHumansSettore BIO/10Caenorhabditis elegansOlive OilReactive oxygen speciesBlood CellsElectrode Potentialslcsh:RElectron Spin Resonance SpectroscopyChemical CompoundsBiology and Life SciencesCell BiologyAgronomyDietRatsTyrosolOxidative Stress030104 developmental biologychemistryHydroxytyrosollcsh:QReactive Oxygen SpeciesOilsOxidative stressCrop Science
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Rate Theory for Electrocatalytic Systems: Fixed Potential Formulation for General, Electron Transfer, and Proton-Coupled Electron Transfer Reactions

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 gene…

Canonical ensembleTransition state theoryElectron transferGrand canonical ensembleMaterials scienceStandard electrode potentialElectrochemical kineticsThermodynamicsRate equationProton-coupled electron transfer
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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…

Canonical ensembleTransition state theoryGrand canonical ensembleElectron transferMaterials scienceStandard electrode potentialThermodynamicsRate equationProton-coupled electron transferElectrode potential
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Electrical impedance spectroscopy of ionic liquid 1-ethyl-3-methylimidazolium methanesulfonate (ECOENG™ 110)

2011

Abstract Ionic liquid “ECOENG™ 110”, a promising electrolyte for electrochemical devices, was investigated by impedance spectroscopy. Metallic electrodes (Pt, Cu, Ag, and Mo) as well as carbon were used for the electrochemical characterization. The dependences of the real and imaginary impedance, polarization resistance and electrochemical capacity of the double layer on the electrode potential were investigated using electrical equivalent circuits of R1(QR2) and R1[Q(R2W)] types.

ChemistryAnalytical chemistryGeneral ChemistryElectrolyteCondensed Matter PhysicsElectrochemistryDielectric spectroscopychemistry.chemical_compoundIonic liquidEquivalent circuitGeneral Materials SciencePolarization (electrochemistry)Electrical impedanceElectrode potentialSolid State Ionics
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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 …

ChemistryGeneral Chemical EngineeringAnalytical chemistryElectrochemical kineticsThermodynamicsTortuosityAnalytical ChemistryElectron transferMass transferElectrodeElectrochemistryRotating disk electrodePorosityElectrode potentialJournal of Electroanalytical Chemistry
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Solvent-Independent Electrode Potentials of Solids Undergoing Insertion Electrochemical Reactions: Part I. Theory

2012

A formally solvent-independent redox system can be theoretically defined using the Lovric and Scholz modeling of the voltammetry of microparticles for ion-insertion solids. The proposed theory is based on the extra-thermodynamic assumptions that no net charge accumulates at the solid|electrolyte interface and the assumption that the structure of the solid and the ion binding remain unaffected by the solvent. Under voltammetric conditions, the corresponding redox potential can be estimated from voltammetric and chronoamperometric data assuming electrochemical reversibility and diffusive charge transport in the solution and solid phases, also taking into account ion partition (electrolyte/sol…

ChemistryInorganic chemistryThermodynamicsElectrolyteElectrochemistryRedoxSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonSolventGeneral EnergyIon bindingStandard electrode potentialPhysics::Chemical PhysicsPhysical and Theoretical ChemistryVoltammetryThe Journal of Physical Chemistry C
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Deposition of Cu Nanoparticles on the Surface of Metallic Aluminum

2012

Deposition of Cu particles by electrolysis at constant electrode potential and by internal electrolysis methods was investigated. The composition of deposited material was confirmed by optical and scanning electron microscope methods. Combination of electrolysis at constant electrode potential with internal electrolysis method was found most effective for fabrication of nanoparticle arrays. Single crystalline Cu particles are fabricated by internal electrolysis, while polycrystalline ones obtained by combined chronopotentiometric and internal electrolysis methods. The formation mechanism of Cu nanoparticles is described.

Cu nanoparticlesElectrolysisFabricationMaterials scienceChemical engineeringlawScanning electron microscopeAnalytical chemistryNanoparticleCrystalliteDeposition (law)law.inventionElectrode potentialIOP Conference Series: Materials Science and Engineering
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The nanoscale structure of the Pt-water double layer under bias revealed

2019

The nanoscopic mass and charge distribution within the double layer at electrified interfaces plays a key role in electrochemical phenomena of huge technological relevance for energy production and conversion. However, in spite of its importance, the nanoscopic structure of the double layer and its response to an applied potential is still almost entirely unknown, even for Pt-water, the most fundamental electrochemical interface. Using a general ab initio methodology which advances previous models towards a dynamic and more realistic description of an electrode/electrolyte interface, we simulate for the first time the nanoscopic structure of the Pt-water double layer and its response to an …

Double layer (biology)Chemical Physics (physics.chem-ph)Condensed Matter - Materials ScienceMaterials scienceGeneral Chemical EngineeringAbsolute electrode potentialCharge densityMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciences02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyElementary charge01 natural sciencesCapacitance0104 chemical sciencesDipoleChemical physicsPhysics - Chemical PhysicsElectrodeElectrochemistry0210 nano-technologyLayer (electronics)
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