Search results for "electrochemical cell"

showing 10 items of 104 documents

A comparative evaluation of palladium and platinum nanoparticles as catalysts in proton exchange membrane electrochemical cells

2008

The goal of the present study is the development and comparative characterisation of carbon-supported and nanostructured Pd- and Pt-based electrocatalysts for hydrogen oxidation in Proton Exchange Membrane (PEM) H2/O2(air) fuel cells and proton reduction in PEM water electrolysers. Catalysts have been synthesised in a solution using a combined impregnation/reduction polyol method. They have been characterised using X-ray Diffraction (XRD) analysis, Transmission Electron Microscopy (TEM), Thermogravimetric Analysis (TGA) and cyclic voltammetry. NanoPt, nanoPd and nanoPt-Pd catalysts deposited onto a carbon carrier have been used to prepare Membrane-Electrode Assemblies (MEAs) which, in turn,…

ElectrolysisMaterials scienceElectrolysis of waterElectrolytic celllawInorganic chemistryProton exchange membrane fuel cellCyclic voltammetryElectrochemistryDirect-ethanol fuel cellElectrochemical celllaw.inventionInternational Journal of Nuclear Hydrogen Production and Applications
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Adiabatic versus Non-Adiabatic Electron Transfer at 2D Electrode Materials

2021

<div><div><div><p>Outer-sphere electron transfer (OS-ET) is a cornerstone elementary electrochemical reaction, yet microscopic understanding is largely based on idealized theories, developed in isolation from experiments that themselves are often close to the kinetic (diffusion) limit. Focusing on graphene as-grown on a copper substrate as a model 2D material/metal-supported electrode system, this study resolves the key electronic interactions in OS-ET, and identifies the role of graphene in modulating the electronic properties of the electrode/electrolyte interface. An integrated experimental-theoretical approach combining co-located multi-microscopy, centered on sc…

Electron transferMaterials scienceGraphenelawChemical physicsBilayerMonolayerOuter sphere electron transferDensity functional theoryBilayer graphenelaw.inventionElectrochemical cell
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Ionic multiresonant thermally activated delayed fluorescence emitters for light emitting electrochemical cells

2022

Funding: M. K. would like to thank 2214-A International Research Fellowship Programme for Ph.D. students (1059B141900585). This project has received funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska Curie grant agreement No 838885 (NarrowbandSSL). S.M.S. acknowledges support from the Marie Skłodowska-Curie Individual Fellowship (grant agreement No 838885 NarrowbandSSL). A. K. G. is grateful to the Royal Society for Newton International Fellowship NF171163. L.M acknowledges that the project who gave rise to these results received support from the European Research Council (ERC) under the European Union’s Horizon 2020 research and inno…

ElectroquímicaMultiresonancePurely organic emittersMCCThermally activated delayed fluorescenceElectroluminescenceLight-emitting electrochemical cellsOrganic ChemistryDASQDQD ChemistryQuímica orgànica
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Electrochemical oxidation of organics in water: Role of operative parameters in the absence and in the presence of NaCl

2008

The electrochemical oxidation of organics in water was investigated theoretically and experimentally to determine the role of several operative parameters on the performances of the process in the presence and in the absence of sodium chloride. Theoretical considerations were used to design the experimental investigation and were confirmed by the results of the electrochemical oxidation of oxalic acid (OA) at boron doped diamond (BDD) or IrO(2)-Ta(2)O(5) (DSA-O(2)) anodes in a continuous batch recirculation reaction system equipped with a parallel plate undivided electrochemical cell. Polarization curves and chronoamperometric measurements indicated that, in the presence of chlorides, the a…

Environmental EngineeringInorganic chemistryOxalic acidIncinerationSodium ChlorideElectrochemistryChemical reactionChlorideElectrolysisElectrochemical celllaw.inventionchemistry.chemical_compoundlawElectrochemical incinerationeSodium chlorideOxalic acidBDDDSAOxidation of organicsmedicineOrganic ChemicalsPolarization (electrochemistry)Waste Management and DisposalWater Science and TechnologyCivil and Structural EngineeringBoronElectrolysisEcological ModelingOxalic AcidElectric ConductivityWaterElectrochemical TechniquesHydrogen-Ion ConcentrationSettore ING-IND/27 - Chimica Industriale E TecnologicaPollutionAnodeSolutionschemistryChlorineDiamondRheologyOxidation-Reductionmedicine.drug
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2016

The structure–property relationship study of a series of cationic Ir(III) complexes in the form of [Ir(C^N)2(dtBubpy)]PF6 [where dtBubpy = 4,4′-di-tert-butyl-2,2′-bipyridine and C^N = cyclometallating ligand bearing an electron-withdrawing group (EWG) at C4 of the phenyl substituent, i.e., −CF3 (1), −OCF3 (2), −SCF3 (3), −SO2CF3 (4)] has been investigated. The physical and optoelectronic properties of the four complexes were comprehensively characterized, including by X-ray diffraction analysis. All the complexes exhibit quasireversible dtBubpy-based reductions from −1.29 to −1.34 V (vs SCE). The oxidation processes are likewise quasireversible (metal + C^N ligand) and are between 1.54 and …

FabricationChemistryStereochemistryLigandCationic polymerizationSubstituent02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesInorganic ChemistryMetalchemistry.chemical_compoundCrystallographyvisual_artvisual_art.visual_art_mediumPolar effectLight-emitting electrochemical cellPhysical and Theoretical ChemistryAbsorption (chemistry)0210 nano-technologyInorganic Chemistry
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Electrical characterization of deoxyribonucleic acid hybridization in metal-oxide-semiconductor-like structures

2012

In this work, metal-oxide-semiconductor (MOS)-like sensors in which deoxyribonucleic acid (DNA) strands are covalently immobilized either on Si oxide or on a gold surface were electrically characterized. Si oxide fabrication process allowed us to have a surface insensitive to the solution pH. A significant shift in the flat band voltage was measured after single strand DNA immobilization (+0.47 +/- 0.04 V) and after the complementary strand binding (+0.07 +/- 0.02 V). The results show that DNA sensing can be performed using a MOS structure which can be easily integrated in a more complex design, thus avoiding the problems related to the integration of micro-electrochemical cells.

FabricationMaterials scienceComplementary strandPhysics and Astronomy (miscellaneous)OxideNanotechnologyElectrical characterizationSettore ING-INF/01 - ElettronicaComplex designSIO2 SURFACESMetalSi oxidechemistry.chemical_compoundCAPACITORSComplementary DNASolution pHFlat-band voltageMicro-electrochemical cellFIELD-EFFECT DEVICESMolecular biophysicsMetal oxide semiconductorDNAGold surfaceMOS structureIMMOBILIZATIONChemical engineeringchemistryFabrication proceCovalent bondvisual_artvisual_art.visual_art_mediumSingle strand DNABiosensorDNADNA sensing
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Front Cover: CF3 Substitution of [Cu(P^P)(bpy)][PF6 ] Complexes: Effects on Photophysical Properties and Light-Emitting Electrochemical Cell Performa…

2018

Front coverMaterials sciencechemistrySubstitution (logic)chemistry.chemical_elementChelationGeneral ChemistryLight-emitting electrochemical cellPhotochemistryElectrochemistryCopperChemPlusChem
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INFLUENCE OF THE EXPERIMENTAL SYSTEM AND OPTIMIZATION OF THE SELECTIVITY FOR THE ELECTROCARBOXYLATION OF CHLOROACETONITRILE TO CYANOACETIC ACID

2004

The electrocarboxylation of chloroacetonitrile (ClACN) to cyanoacetic acid in undivided cells equipped with sacrificial anodes was investigated both in a bench-scale electrochemical batch reactor and in a continuous batch recirculation reaction system equipped with a parallel-plate electrochemical cell. Selectivity and faradaic yields higher than 90% were obtained by working under anhydrous conditions with low halide concentrations and at more negative potentials. It was found that the instantaneous selectivity in the carboxylate compound depends mainly on the [CO 2 ]/[ClACN] ratio at high substrate concentration and is close to 100% for low ClACN concentration. These results were consisten…

General Chemical EngineeringInorganic chemistryBatch reactorSubstrate (chemistry)General ChemistrySettore ING-IND/27 - Chimica Industriale E TecnologicaElectrochemistryIndustrial and Manufacturing EngineeringElectrochemical cellchemistry.chemical_compoundcarboxylation father-son reactionCyanoacetic acidchemistryCarboxylationOrganic chemistryCarboxylateSelectivity
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Green Light-Emitting Solid-State Electrochemical Cell Obtained from a Homoleptic Iridium(III) Complex Containing Ionically Charged Ligands

2006

An efficient bluish-green light-emitting Ir(III) complex was prepared by introducing charged side groups onto phenylpyridine ligands. Green light emission with a first maximum at 487 nm (CIE coordinates x = 0.337 and y = 0.501) was observed from a single layer light-emitting electrochemical cell using this new complex; this is the lowest wavelength observed so far for devices based on ionic transition metal complexes.

General Chemical EngineeringInorganic chemistrySolid-stateIonic bondingchemistry.chemical_elementGeneral ChemistryGreen-lightPhotochemistryElectrochemical cellchemistry.chemical_compoundWavelengthTransition metalchemistryMaterials ChemistryIridiumHomolepticChemistry of Materials
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An electrochemical quartz crystal microbalance study of lithium insertion into thin films of tungsten trioxide I. Modeling of the ionic insertion mec…

1995

A theoretical description of the mechanism of lithium insertion into amorphous thin films of tungsten trioxide (a-WO3) prepared by thermal vacuum evaporation of WO3 powder is presented. The model developed is based on the experimental results obtained by chronoamperometry and ac impedance spectroscopy associated with electrochemical quartz crystal microbalance (EQCM). The electrode mass change and the current flowing through the electrochemical cell during cathodic polarization are simulta neously recorded. As expected, it can be observed that the insertion process is associated with a gain of mass of the inserted electrode at long times (t > 1 s). On the other hand at short times (t < 1 s)…

General Chemical EngineeringInorganic chemistrychemistry.chemical_elementQuartz crystal microbalanceChronoamperometryTungsten trioxideLithium perchlorateElectrochemical cellAmorphous solidchemistry.chemical_compoundchemistryElectrodeElectrochemistryLithiumElectrochimica Acta
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