Search results for "electrochromism"

showing 10 items of 50 documents

Coloration mechanism of electrochromic Na x WO3 thin films

2019

International audience; The coloration mechanism of tungsten trioxide (WO3) upon insertion of alkali ions is still under debate after several decades of research. This Letter provides new insights into the reversible insertion and coloration mechanisms of Na+ ions in WO3 thin films sputter-deposited on ITO/glass substrates. A unique model based on a constrained spline approach was developed and applied to draw out ε1+iε2 from spectroscopic ellipsometry data from 0.6 to 4.8 eV whatever the state of the electrochromic active layer, i.e. as-deposited, colored or bleached. It is shown that electrochemically intercalated sodium-tungsten trioxide, NaxWO3 (x=0.1, 0.2, 0.35), exhibits an absorption…

010302 applied physicsAlkali ions[PHYS]Physics [physics]Materials sciencebusiness.industry02 engineering and technology021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesTungsten trioxideAtomic and Molecular Physics and OpticsActive layerIonchemistry.chemical_compoundOpticschemistryElectrochromismAbsorption band0103 physical sciences[CHIM]Chemical SciencesThin film0210 nano-technologybusinessTrioxide
researchProduct

Spectroscopic and electrochromical properties of metallophthalocyanines in silicate bulks and thin films prepared by the sol–gel method

2000

Abstract Magnesium phthalocyanine (MgPc) and praseodymium bisphthalocyanine (Pr(Pc) 2 ) have been entrapped in bulks and thin films of porous silicate xerogels prepared via the sol–gel method. The electronic absorption data obtained for the complexes immobilized in bulk sol–gel matrices indicate the formation of complex equilibria between their monomeric forms and respective agglomerates. Thin xerogel films doped with metallophthalocyanines and connecting two slides of transparent ITO electrodes display changes in the absorption spectra caused by varying of the applied voltage. These changes appear to be reversible in certain ranges of the applied voltages.

Absorption spectroscopyPraseodymiumOrganic ChemistryInorganic chemistrychemistry.chemical_elementSilicateAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundchemistryElectrochromismPhthalocyanineThin filmAbsorption (chemistry)SpectroscopySol-gelJournal of Molecular Structure
researchProduct

Kinetics of coloration of anodic electrochromic films of WO3·H2O

1980

Polycrystalline layers of WO3·H2O are obtained by anodization of tungsten in 1 N H2SO4 at 70° C. The cathodic reduction of these layers in acid solutions causes the formation of blue WO3−x·H2O (0<x⩽:0.12) oxides. The kinetics of coloration are investigated by galvanostatic and potentiostatic techniques. The experimental results are compared with the theoretical data obtained by solving the diffusion equation for a constant flow of oxygen vacancies and for a time-dependent surface vacancy concentration. Except in the initial stage of coloration, the process controlling rate can be ascribed to the diffusion of oxygen vacancies from the oxide-electrolyte interface into the bulk of the layers. …

AnodizingChemistryGeneral Chemical EngineeringDiffusionKineticsAnalytical chemistrychemistry.chemical_elementTungstenElectrochemistryElectrochromismVacancy defectMaterials ChemistryElectrochemistryCrystalliteJournal of Applied Electrochemistry
researchProduct

Vis/NIR spectroelectrochemical analysis of poly-(Azure A) on ITO electrode

2006

Electrochromic behavior of poly-(Azure A) on indium–tin oxide electrode is analyzed in an aqueous potassium nitrate solution. The dependence of the absorbance on the applied potential during cyclic voltammograms proves very interesting at two selected characteristic wavelengths: at 925 nm, attributed to an intermediate species and another at 735 nm, attributed to the oxidized form of the polymer. Molar absorptivity coefficients for both species have been calculated from the relationship between current and the derivative of absorbance with respect to time. Voltammograms of formation of the intermediate are simulated from spectroelectrochemical results. Keywords: Poly-(Azure A), Spectroelect…

Aqueous solutionAnalytical chemistryAzure APotassium nitrateMolar absorptivitylcsh:ChemistryAbsorbancechemistry.chemical_compoundlcsh:Industrial electrochemistrylcsh:QD1-999chemistryElectrochromismElectrodeElectrochemistryCyclic voltammetrylcsh:TP250-261
researchProduct

&lt;title&gt;Electrochromism in oxyfluoride thin films&lt;/title&gt;

1994

Oxyfluoride films based on W and Ti were prepared by reactive sputtering in plasmas containing O2 + CF4. The deposition rate was large, particularly when chemical sputtering was promoted by heating the target. The films could show large charge insertion/extraction, high coloration efficiency, and good cycling durability.© (1994) COPYRIGHT SPIE--The International Society for Optical Engineering. Downloading of the abstract is permitted for personal use only.

ArgonMaterials sciencebusiness.industryInorganic chemistrychemistry.chemical_elementSputter depositionIonsymbols.namesakechemistryElectrochromismSputteringsymbolsOptoelectronicsLithiumThin filmRaman spectroscopybusinessSPIE Proceedings
researchProduct

Recent Advances in Electrochromics for Smart Windows Applications

1998

Electrochromic smart windows are able to vary their throughput of radiant energy by low-voltage electrical pulses. This function is caused by reversible shuttling of electrons and charge balancing ions between an electrochromic thin film and a transparent counter electrode. The ion transport takes place via a solid electrolyte. Charge transport is evoked by a voltage applied between transparent electrical conductors surrounding the electrochromic film/electrolyte/counter electrode stack. This review summarizes recent progress concerning (i) calculated optical properties of crystalline WO3, (ii) electrochromic properties of heavily disordered W oxide and oxyfluoride films produced by reactiv…

Auxiliary electrodeMaterials scienceRenewable Energy Sustainability and the Environmentbusiness.industryOxideElectrolytechemistry.chemical_compoundchemistrySputteringElectrochromismElectrodeOptoelectronicsGeneral Materials ScienceThin filmbusinessElectrical conductorOptical Interference Coatings
researchProduct

&lt;title&gt;Performance problems of electrochromic coatings&lt;/title&gt;

2003

The performance is actual problem of electrochromic coatings. The service and shelf life and cycling capacity are main performance characteristics. By solid-state ionics point of view any electrochromic cell based on phenomena with ion insertion - extraction processes is functioning as solid-state rechargeable battery. The main performance characteristics of electrochromic cells are similar. Performance of electrochromic coatings based on amorphous WO3 films and protons conducting electrolytes is limited by reversibility of ion insertion-extraction reactions, which causes degradation of cell components. The migration of water in the cell and hydration together with ion insertion-extraction …

Battery (electricity)Materials scienceOptical coatingChemical engineeringchemistryElectrochromismElectrodeForensic engineeringchemistry.chemical_elementElectrolyteTungstenAmorphous solidIonSPIE Proceedings
researchProduct

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…

Carbonsäuren Monoschicht PolymercompoundAuxiliary electrodeMaterials scienceElectrolytic cellMechanical EngineeringAnalytical chemistryElectrolyteElectrochemistry540Reference electrodeElectrochemical cellMechanics of MaterialsElectrochromismElectrodeGeneral Materials Science
researchProduct

Electrosynthesis of Ce–Co Mixed Oxide Nanotubes with High Aspect Ratio and Tunable Composition

2008

Cerium oxide and cobalt oxides have attracted the interest of several researchers due to their potential application in several technological fields electrochromism, lithium batteries, catalysis, etc.. Ceria has been used as a promoter in the so-called “three-way catalyst” for the control of toxic emission from automobile exhaust. The promotion consists of the enhancement of the noble metal dispersion, as well as stabilization of the supporting medium toward thermal sintering. 1,2 A direct catalytic effect of CeO2 in chemical processes such as water–gas shift reaction or NOx decomposition has been also evidenced. 3,4

Cerium oxideMaterials scienceALUMINA MEMBRANESGeneral Chemical EngineeringInorganic chemistrychemistry.chemical_elementCATALYSTSengineering.materialElectrosynthesisFUEL-CELLSCatalysisTEMPLATEElectrochemistryGeneral Materials ScienceElectrical and Electronic EngineeringPhysical and Theoretical ChemistryNOxCERIUM OXIDE; COBALT OXIDE; ALUMINA MEMBRANES; FUEL-CELLS; CATALYSTS; TEMPLATE; SPECTROSCOPY; ELECTROLYTES; MORPHOLOGYCerium cobalt mixed oxide nanotubeSPECTROSCOPYElectrochemical Template assisted electrosyntesisELECTROLYTESCOBALT OXIDESettore ING-IND/23 - Chimica Fisica ApplicatachemistryElectrochromismengineeringMixed oxideMORPHOLOGYNoble metalCERIUM OXIDECobalt
researchProduct

Electrochromic absorbance changes in the chlorophyll-c-containing alga Pleurochloris meiringensis (Xanthophyceae)

1994

Flash-induced absorbance changes were measured in the Chl-c-containing alga Pleurochloris meiringensis (Xanthophyceae) between 430 and 570 nm. In addition to the bands originating from redox changes of cytochromes, three major positive and tow negative transient bands were observed both 0.7 and 20 ms after the exciting flash. These transient bands peaking at 520, 480 and 451 nm and 497 and 465 nm, respectively, could be assigned to an almost homogeneous shift of the absorbance bands with maxima at 506, 473 and 444 nm, respectively. The shape of the absorbance transients elicited from PS I or PS II was identical, and the two photosystems contributed nearly equally to the absorbance changes. …

ChemistryAnalytical chemistryChlorophyll cDiatoxanthinCell BiologyPlant ScienceGeneral MedicinePhotochemistryBiochemistryFluorescenceAbsorbancePigmentchemistry.chemical_compoundElectrochromismAbsorption bandvisual_artvisual_art.visual_art_mediumPhotosystemPhotosynthesis Research
researchProduct