Search results for "electrochemical"

showing 10 items of 574 documents

Ionic and Free Solvent Motion in Poly(azure A) Studied by ac-Electrogravimetry

2011

International audience; This work is focused on the mechanistic aspects of the redox behavior of poly(azure A) taking advantage of the controlled modulation of their oxidation states by ac-electrogravimetry. The originality of this technique is its ability to discriminate between cation and anion involved in the charge compensation process and the accompanying free solvent transfer, directly or indirectly. Two processes were proposed where the faster ionic exchange is considered to be the participation of the anion species acting as counterions whereas the slower one is related to the proton transfer. The proton is implied as reactants for the two electroactive sites identified in the polym…

Inorganic chemistryIonic bondingAzure A02 engineering and technology010402 general chemistry01 natural sciencesRedoxIonchemistry.chemical_compoundQUARTZ-CRYSTAL MICROBALANCEElectrogravimetryPOLYMER-MODIFIED ELECTRODESPhysical and Theoretical ChemistryELECTROACTIVE THIN-FILMSchemistry.chemical_classificationAqueous solutionPRUSSIAN BLUE021001 nanoscience & nanotechnologyPOLY(NEUTRAL RED)0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSolventGeneral EnergyELECTROCHEMICAL POLYMERIZATIONTECHNIQUES ELECTRICAL CHARGEchemistryCONDUCTING POLYMERSCounterion[CHIM.OTHE]Chemical Sciences/Other0210 nano-technologyELECTROPOLYMERIZED AZINESINNOVATIVE COMBINATIONThe Journal of Physical Chemistry C
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Dynamics of closure of zinc bis-porphyrin molecular tweezers with copper(II) ions and electron transfer.

2011

Zinc bis-porphyrin molecular tweezers composed of a N(4) spacer bound through pyridyl units to the meso position of porphyrins were synthesized, and the tweezers are closed by the coordination of a copper(II) ion inside the spacer ligand. The effect of the π-π interaction between the porphyrin rings in the closed conformation on the absorption spectra of multi-electron oxidized species and the reduction potentials were clarified by chemical and electrochemical oxidation of the closed form of the zinc bis-porphyrin molecular tweezers in comparison with the open form without copper(II) ion and the corresponding porphyrin monomer. The shifts in redox potentials and absorption spectrum of the p…

IonsLigandMetalloporphyrinsOrganic Chemistrychemistry.chemical_elementGeneral ChemistryZincElectrochemical TechniquesPhotochemistryPorphyrinCopperCatalysisDicationElectron TransportElectron transferchemistry.chemical_compoundchemistryTweezerspolycyclic compoundsheterocyclic compoundsSpectrophotometry UltravioletMolecular tweezersOxidation-ReductionCopperChemistry (Weinheim an der Bergstrasse, Germany)
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Luminescent Ionic Transition-Metal Complexes for Light-Emitting Electrochemical Cells

2012

Higher efficiency in the end-use of energy requires substantial progress in lighting concepts. All the technologies under development are based on solid-state electroluminescent materials and belong to the general area of solid-state lighting (SSL). The two main technologies being developed in SSL are light-emitting diodes (LEDs) and organic light-emitting diodes (OLEDs), but in recent years, light-emitting electrochemical cells (LECs) have emerged as an alternative option. The luminescent materials in LECs are either luminescent polymers together with ionic salts or ionic species, such as ionic transition-metal complexes (iTMCs). Cyclometalated complexes of Ir(III) are by far the most util…

IonsMaterials scienceLuminescenceLightMolecular StructureIonic bondingNanotechnologycopper(I) complexes; electroluminescence; iridium(III) complexes; light-emitting electrochemical cells; ruthenium(II) complexesGeneral ChemistryElectrochemical TechniquesElectroluminescenceCatalysisElectrochemical celllaw.inventionTransition metallawOLEDOrganometallic CompoundsTransition ElementsLuminescenceLight-emitting diodeDiode
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Impact of Surface Charge Directionality on Membrane Potential in Multi-ionic Systems

2020

The membrane potential (Vmem), defined as the electric potential difference across a membrane flanked by two different salt solutions, is central to electrochemical energy harvesting and conversion. Also, Vmem and the ionic concentrations that establish it are important to biophysical chemistry because they regulate crucial cell processes. We study experimentally and theoretically the salt dependence of Vmem in single conical nanopores for the case of multi-ionic systems of different ionic charge numbers. The major advances of this work are (i) to measure Vmem using a series of ions (Na+, K+, Ca2+, Cl-, and SO42-) that are of interest to both energy conversion and cell biochemistry, (ii) to…

IonsMembrane potentialChemistryIonic bondingElectrochemical Techniques02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesElectrochemical energy conversionMembrane Potentials0104 chemical sciencesIonNanoporesMembraneChemical physicsGeneral Materials ScienceSurface chargeElectric potentialPhysical and Theoretical Chemistry0210 nano-technologyBiophysical chemistryThe Journal of Physical Chemistry Letters
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Bright Blue Phosphorescence from Cationic Bis-Cyclometalated Iridium(III) Isocyanide Complexes

2012

We report new bis-cyclometalated cationic indium(III) complexes [((CN)-N-boolean AND)(2)Ir(CN-tert-Bu)(2)](CF3SO3) that have tert-butyl isocyanides as neutral auxiliary ligands and 2-phenylpyridine or 2-(4'-fluoropheny1)-R-pyridines (where R is 4-methoxy, 4-tert-butyl, or 5-trifluoromethyl) as (CN)-N-boolean AND ligands. The complexes are white or pale yellow solids that show irreversible reduction and oxidation processes and have a large electrochemical gap of 3.58-3.83 V. They emit blue or bluegreen phosphorescence in liquid/solid solutions from a cyclometalating-ligand-centered excited state. Their emission spectra show vibronic structure with the highest-energy luminescence peak at 440-…

Ir(Iii) ComplexesIsocyanideCationic polymerizationchemistry.chemical_elementEmitting Electrochemical-CellsExcited-State PropertiesElectroluminescent DevicesPhotochemistryAncillary LigandsInorganic Chemistrychemistry.chemical_compoundchemistryExcited stateEfficient BlueIii ComplexesMetal-ComplexesEmission spectrumIridiumPhysical and Theoretical ChemistryPhosphorescenceLuminescenceTurn-On TimesPhotophysical PropertiesSolid solutionInorganic Chemistry
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Redox tuning and species distribution in Maya Blue-type materials: a reassessment.

2013

Maya Blue-type specimens prepared from indigo (1 wt %) plus kaolinite, montmorillonite, palygorskite, sepiolite, and silicalite are studied. Liquid chromatography with diode array detection, ultra-performance liquid chromatography coupled with mass spectrometry, and pyrolysis-silylation gas chromatography-mass spectrometry analyses of the extracts from these specimens combined with spectral and solid-state voltammetry, electrochemical impedance spectroscopy, and scanning electrochemical microscopy techniques provide evidence for the presence of a significant amount of dehydroindigo and isatin accompanying indigo and other minority organic compounds in all samples. Solid-state electrochemist…

Isatingas chromatography mass spectrometryMagnesium CompoundsMass spectrometryIndigo CarmineUPLC-MSIndigoMass Spectrometrychemistry.chemical_compoundScanning electrochemical microscopyMagnesium SilicatesmedicineElectrochemistryHumansGeneral Materials ScienceKaolinChromatography High Pressure LiquidMaya BlueChromatographyChemistryIsatinSilicon CompoundsPalygorskitevoltammetry of microparticlesDielectric spectroscopyMontmorillonitePINTURABentoniteGas chromatography–mass spectrometryOxidation-Reductionmedicine.drugNuclear chemistryChromatography LiquidACS applied materialsinterfaces
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Scanning electrochemical microscopy as a probe of Ag+ binding kinetics at Langmuir phospholipid monolayers

2005

A new method has been developed for measuring local adsorption rates of metal ions at interfaces based on scanning electrochemical microscopy (SECM). The technique is illustrated with the example of Ag+ binding at Langmuir phospholipid monolayers formed at the water/air interface. Specifically, an inverted 25 microm diameter silver disc ultramicroelectrode (UME) was positioned in the subphase of a Langmuir trough, close to a dipalmitoyl phosphatidic acid (DPPA) monolayer, and used to generate Ag+ via Ag electro-oxidation. The method involved measuring the transient current-time response at the UME when the electrode was switched to a potential to electrogenerate Ag+. Since the Ag+/Ag couple…

LangmuirBinding SitesSilverTime FactorsSurface PropertiesChemistryMetal ions in aqueous solutionAnalytical chemistryPhosphatidic AcidsGeneral Physics and AstronomyUltramicroelectrodeMicroscopy Scanning ProbeSurface pressureKineticsScanning electrochemical microscopyAdsorptionCationsElectrodeMonolayerElectrochemistrylipids (amino acids peptides and proteins)AdsorptionPhysical and Theoretical ChemistryPhospholipidsPhysical Chemistry Chemical Physics
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Comments on 'formation and characterization of nanotubes of La(OH) 3 obtained using porous alumina membranes'

2010

New experimental evidence concerning the formation of La(OH)3 nanowires on anodic alumina membranes by cathodic polarization in 0.05 M lanthanum nitrate solution is provided to further support the conclusions previously reached in our work (Bocchetta et al 2007 Electrochem. Commun. 9 683-8) and recently criticized by González-Rovira et al (Nanotechnology 2008 19 495305). Some unconvincing aspects of the paper of González-Rovira et al, according to which the same electrochemical process should lead to the formation of hydroxycarbonate nanotubes, are also discussed.

Lanthanum nitrateMaterials scienceMechanical EngineeringAlumina membranesNanowireBioengineeringNanotechnologyCathodic polarizationGeneral ChemistryElectrochemistryAnodeCharacterization (materials science)Settore ING-IND/23 - Chimica Fisica ApplicataChemical engineeringLa(OH)3 nanowireelectrogeneration of base anodic alumina membraneMechanics of MaterialsAnodic alumina membranes Electrochemical process Experimental evidence Hydroxy carbonates Lanthanum nitrates Porous alumina membranesGeneral Materials ScienceElectrical and Electronic EngineeringPorosity
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Detection of archaeological forgeries of Iberian lead plates using nanoelectrochemical techniques. The lot of fake plates from Bugarra (Spain)

2014

Identification of forgeries is of considerable interest in studies of archaeological signariums and written Iberian artifacts, elements of capital importance for the knowledge of that culture, because there are many Iberian inscribed lead plate counterfeits circulating in the market and among many museum funds. A case study of identification of forgeries of archaeological lead using voltammetry of microparticles (VMP) and scanning electrochemical microscopy (SECM), aided by conventional optical microscopy and scanning electron microscopy (SEM/EDX) is described. The electrochemical methods are essentially non-invasive so can be applied to samples of nanoscopic size. Application to the authen…

Lead inscriptions IberianScanning electrochemical microscopyVoltammetry of microparticlesArchaeologyPalaeographyPathology and Forensic MedicineScanning electrochemical microscopyLead plateArchaeologyPINTURALawGeologyHeritage authentication
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Highly Stable Red-Light-Emitting Electrochemical Cells

2017

The synthesis and characterization of a series of new cyclometalated iridium(III) complexes [Ir(ppy) 2 (N ∧ N)][PF 6 ] in which Hppy = 2-phenylpyridine and N ∧ N is (pyridin-2-yl)benzo[ d ]thiazole ( L1 ), 2-(4-( tert -butyl)pyridin-2-yl)benzo[ d ]thiazole ( L2 ), 2-(6-phenylpyridin-2-yl)benzo[ d ]thiazole ( L3 ), 2-(4-( tert -butyl)-6-phenylpyridin-2-yl)benzo[ d ]thiazole ( L4 ), 2,6-bis(benzo[ d ]thiazol-2-yl)pyridine ( L5 ), 2-(pyridin-2-yl)benzo[ d ]oxazole ( L6 ), or 2,2′-dibenzo[ d ]thiazole ( L7 ) are reported. The single crystal structures of [Ir(ppy) 2 ( L1 )][PF 6 ]·1.5CH 2 Cl 2 , [Ir(ppy) 2 ( L6 )][PF 6 ]·CH 2 Cl 2 , and [Ir(ppy) 2 ( L7 )][PF 6 ] have been determined. The new com…

LigandStereochemistrychemistry.chemical_element02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistryMedicinal chemistryCatalysis0104 chemical sciencesElectrochemical cellchemistry.chemical_compoundColloid and Surface ChemistrychemistryPyridineRed lightIridium0210 nano-technologyThiazoleSingle crystalOxazoleJournal of the American Chemical Society
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