Search results for "ionic conductivity"

showing 10 items of 56 documents

Hydrothermal synthesis of nanostructured zirconia materials: Present state and future prospects

2005

Abstract Hydrothermal procedures for the synthesis of zirconia-doped nanocrystalline powders show important advantages from the thermodynamic and kinetic point of view (larger domain stability of solid species, faster kinetics crystallisation) as well as from technological point of view (one-step synthesis process at low temperatures, better control of the crystallisation and grain sizes with possibilities to obtain nanocrystalline materials, versatility, environmental friendly technology). Establishment of the conditions for obtaining ZrO2-doped with different oxides is based on thermodynamic predictions. Kinetic modelling of the hydrothermal synthesis of zirconia nanopowders is presented.…

Materials scienceMetals and AlloysIonic bondingNanotechnologyCondensed Matter PhysicsEnvironmentally friendlyHydrothermal circulationNanocrystalline materialSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsNanomaterialsMaterials ChemistryIonic conductivityHydrothermal synthesisCubic zirconiaElectrical and Electronic EngineeringInstrumentationSensors and Actuators B: Chemical
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Lithium ion conducting PVdF-HFP composite gel electrolytes based on N-methoxyethyl-N-methylpyrrolidinium bis(trifluoromethanesulfonyl)-imide ionic li…

2010

Blends of PVDF-HFP and ionic liquids (ILs) are interesting for application as electrolytes in plastic Li batteries. They combine the advantages of the gel polymer electrolytes (GPEs) swollen by conventional organic liquid electrolytes with the nonflammability, and high thermal and electrochemical stability of ILs. In this work we prepare and characterize PVDF-HFP composite membranes swollen with a solution of LiTFSI in ether-functionalized pyrrolidinium-imide (PYRA12O1). The membranes are filled in with two different types of silica: i) mesoporous SiO2 (SBA-15) and a commercial nano-size one (HiSilTM T700). The ionic conductivity and the electrochemical properties of the gel electrolytes ar…

Materials sciencePVdFEnergy Engineering and Power TechnologyIonic bondingchemistry.chemical_elementElectrolyteIonic liquidchemistry.chemical_compoundIonic conductivityThermal stabilityElectrical and Electronic EngineeringPhysical and Theoretical ChemistryGel polymer electrolyteSettore CHIM/02 - Chimica FisicaChromatographyRenewable Energy Sustainability and the EnvironmentPVdF; Ionic liquids; Pyrrolidinium; Gel polymer electrolytes; Lithium battery; Nanoscale fillersLithium batteryLithium batteryMembraneSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiChemical engineeringchemistryIonic liquidLithiumNanoscale fillerNanoscale fillersPyrrolidinium
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Temperature Effect of Ionic Transition Metal Complex Light-Emitting Electrochemical Cells

2013

ABSTRACTLight-Emitting Electrochemical Cells (LECs) consist of solution processable ionic light-emitting materials and use air stable electrodes. Their operational mechanism relies on both ionic and electronic conduction. The dynamic behavior is primarily determined by the ionic conductivity. Here, we demonstrate that with increasing temperature the LECs turn-on faster yet without decreasing the efficiency. This is due to the activation energy of ionic transport and the temperature independent photoluminescence quantum yields.

Materials sciencePhotoluminescenceChemical engineeringTransition metalElectrodeIonic conductivityIonic bondingActivation energyLuminescencePhotochemistryElectrochemical cellMRS Proceedings
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INTERPRETATION OF POTENTIAL INTERMITTENCE TITRATION TECHNIQUE EXPERIMENTS FOR VARIOUS Li-INTERCALATION ELECTRODES

2002

In this paper we compare two different approaches for the calculation of the enhancement factor Wi , based on its definition as the ratio of the chemical and the component diffusion coefficients for species in mixed-conduction electrodes, originated from the “dilute solution” or “lattice gas” models for the ion system. The former approach is only applicable for small changes of the ion concentration while the latter allows one to consider a broad range of intercalation levels. The component diffusion coefficient of lithium ions has been determined for a series of lithium intercalation anodes and cathodes. A new “enhancement factor” for the ion transport has been defined and its relations to…

Materials sciencePhysics and Astronomy (miscellaneous)Inorganic chemistryIntercalation (chemistry)binary componentCondensed Matter Physicslcsh:QC1-999Interpretation (model theory)Physics::Plasma PhysicsElectrodelattice gas modelionic conductivityLi-ion batteryTitrationlcsh:Physicschemical diffusion coefficientCondensed Matter Physics
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Solid polymer electrolytes from a fluorinated copolymer bearing cyclic carbonate pendant groups

2018

International audience; A poly(vinylidene fluoride-co-(2-oxo-1,3-dioxolan-4-yl)methyl 2-(trifluoromethyl)acrylate) random copolymer, poly(VDF-co-MAF-cyCB), with a MAF-cyCB weight fraction of 59% was synthesized via free radical copolymerization of VDF and MAF-cyCB, which is a methacrylate bearing cyclocarbonate side-chain. This copolymer showed nano-structured morphology, where crystalline PVDF-rich domains co-existed with amorphous poly(VDF-co-MAF-cyCB) segments. Solid polymer electrolytes were further obtained by loading the poly(VDF-co-MAF-cyCB) copolymer with various amounts of LiClO4. The added lithium salt was dissolved in the poly(VDF-co-MAF-cyCB) amorphous phase, which allowed the f…

Materials scienceSustainability and the EnvironmentRenewable Energy Sustainability and the EnvironmentIonic bondingchemistry.chemical_element02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyMethacrylateElectrochemistry01 natural sciences0104 chemical sciencesAmorphous solid[CHIM.POLY]Chemical Sciences/PolymerschemistryChemical engineeringPhase (matter)CopolymerIonic conductivityLithiumGeneral Materials ScienceRenewable Energy0210 nano-technology
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Ionic conduction, rectification, and selectivity in single conical nanopores

2006

Modern track-etching methods allow the preparation of membranes containing a single charged conical nanopore that shows high ionic permselectivity due to the electrical interactions of the surface pore charges with the mobile ions in the aqueous solution. The nanopore has potential applications in electrically assisted single-particle detection, analysis, and separation of biomolecules. We present a detailed theoretical and experimental account of the effects of pore radii and electrolyte concentration on the current-voltage and current-concentration curves. The physical model used is based on the Nernst-Planck and Poisson equations. Since the validity of continuum models for the descriptio…

Models MolecularGeneral Physics and AstronomyIonic bondingRectificationNanotechnologyElectrolytePoisson equationIonElectrolytesBiopolymersIonic conductivityBiomembranesIonic conductivityComputer SimulationPoisson DistributionPhysical and Theoretical ChemistryParticle Size:FÍSICA::Química física [UNESCO]IonsPhysics::Biological PhysicsIon TransportChemistryElectric ConductivityWaterBiological TransportConical surfaceMolecular biophysicsNanostructuresUNESCO::FÍSICA::Química físicaSolutionsNanoporeMembraneBiomembranes ; Bioelectric phenomena ; Ionic conductivity ; Rectification ; Molecular biophysics ; Electrolytes ; Poisson equationChemical physicsBioelectric phenomenaPoisson's equationPorosity
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Ion transport and selectivity in nanopores with spatially inhomogeneous fixed charge distributions

2007

Polymeric nanopores with fixed charges show ionic selectivity when immersed in aqueous electrolyte solutions. The understanding of the electrical interaction between these charges and the mobile ions confined in the inside nanopore solution is the key issue in the design of potential applications. The authors have theoretically described the effects that spatially inhomogeneous fixed charge distributions exert on the ionic transport and selectivity properties of the nanopore. A comprehensive set of one-dimensional distributions including the skin, core, cluster, and asymmetric cases are analyzed on the basis of the Nernst-Planck equations. Current-voltage curves, nanopore potentials, and tr…

Models MolecularMaterials scienceStatic ElectricityGeneral Physics and AstronomyIonic bondingNanotechnologyElectrolyteIon ChannelsNanoporous materialsIonQuantitative Biology::Subcellular ProcessesElectrolytesBiopolymersIonic conductivityStatic electricityCluster (physics)Ionic conductivityComputer SimulationPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]AnisotropyIon TransportUNESCO::FÍSICA::Química físicaNanostructuresNanoporeModels ChemicalPolymer solutionsChemical physicsNanoporous materials ; Polymer solutions ; Electrolytes ; Ionic conductivityAnisotropyIon Channel GatingPorosityThe Journal of Chemical Physics
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Channel Formation and Intermediate Range Order in Sodium Silicate Melts and Glasses

2004

We use inelastic neutron scattering and molecular dynamics simulation to investigate the interplay between the structure and the fast sodium ion diffusion in various sodium silicates. With increasing temperature and decreasing density the structure factors exhibit an emerging prepeak around 0.9 A^-1. We show, that this prepeak has its origin in the formation of sodium rich channels in the static structure. The channels serve as preferential ion conducting pathways in the relative immobile Si-O matrix. On cooling below the glass transition this intermediate range order is frozen in.

Models MolecularSiliconSodiumNeutron diffractionFOS: Physical sciencesGeneral Physics and Astronomychemistry.chemical_elementSodium silicateInelastic scatteringInelastic neutron scatteringIonDiffusionchemistry.chemical_compoundIonic conductivityIonsModels StatisticalPhysicsSilicatesSodiumTemperatureDisordered Systems and Neural Networks (cond-mat.dis-nn)Condensed Matter - Disordered Systems and Neural NetworksOxygenchemistryChemical physicsGlassGlass transitionPhysical Review Letters
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Influence of chain length on the molecular dynamics of an aliphatic ionene

1998

An aliphatic random copolymer ionene (a cationic polyelectrolyte with N + in the repeat unit), was fractionated with the continuous polymer fractionation and investigated for its molecular weight dependent properties. The fractions were analyzed with GPC and capillary viscometry for their molecular weight. Glass transition temperatures were determined with DSC and a strong molecular weight dependence was observed, but no influence in the ionic conductivity was observed. The temperature dependency of ionic conductivity in ionenes is described.

Molecular dynamicsPolymers and PlasticsChemistryGeneral Chemical EngineeringPolymer chemistryCationic polymerizationCopolymerPhysical chemistryViscometerIonic conductivityPolymer fractionationGlass transitionPolyelectrolyteActa Polymerica
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Comparative study of electrical behavior and phase transitions in pure and chromium doped α-LiIO3single crystals

1999

Abstract The polymorphic phase transitions of undoped and chromium doped α-LiIO3 crystals have been investigated by means of DTA experiments at slow heating rates and electrical measurements vs temperature and frequency. Upon heating the well known α ⇔ γ ⇒ β sequence appears to be influenced by the sample's morphology, acidity of the growing solution and doping. Dielectric response at room temperature is close to the type “superposition of d.c. ionic conductivity and dipolar response”. We describe the thermal behavior of conductivity along the c polar axis at three frequencies. Electrical measurements also highlight a higher value of ionic conductivity and a less destructive transition for …

Nuclear and High Energy PhysicsPhase transitionRadiationMaterials scienceInorganic chemistryDopingAnalytical chemistrychemistry.chemical_elementLithium iodateConductivityCondensed Matter PhysicsDipoleChromiumchemistry.chemical_compoundchemistryCondensed Matter::SuperconductivityIonic conductivityGeneral Materials ScienceElectrical measurements
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