0000000000178412

AUTHOR

Fabio Furlan Ferreira

showing 3 related works from this author

Electronic Perspective on the Electrochemistry of Prussian Blue Films

2009

The derivative of the voltabsommetric scans, together with previous nano-electrogravimetric and X-ray diffraction results, allow different electrochemical processes to be distinguished during the Prussian blue (PB) voltammetric scan. Potassium, proton, and hydrated proton counterions involved in PB electrochemistry are related here to the electrochemical reactions of specific Fe sites. Potassium counterions show two different sites for their insertion: one located in the crystalline framework and another in ferrocyanide vacancies. From the monitoring of electroactive Fe sites, the covalent-exchange model is suggested as one of the first approaches to explain the origin of the PB magnetic or…

chemistry.chemical_classificationPrussian blueProtonIon exchangeRenewable Energy Sustainability and the EnvironmentPotassiumInorganic chemistrychemistry.chemical_elementCondensed Matter PhysicsElectrochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryX-ray crystallographyMaterials ChemistryElectrochemistryCounterionFerrocyanideJournal of The Electrochemical Society
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An Electronic Perspective On The Electrochemical Changeover In Prussian Blue-Like Materials

2009

Derivative voltabsometric scans together with previous electrogravimetric results allow to distinguish between the different electrochemical processes due to Fe-sites located into the Prussian Blue crystalline framework and other located next to ferrocyanide vacancies. The potassium, proton and hydrated proton counterions involved in these reactions are correlated to changes in near-UV/VIS/near-IR spectra. Potassium counter-ions show two different sites for insertion: one located into the crystalline framework and the other into ferrocyanide vacancies. From the monitoring of electroactive Fe-sites, it is possible to assume that the reduction of all Fe-sites located next to ferrocyanide vaca…

chemistry.chemical_classificationPrussian blueMaterials scienceSalt (chemistry)ChangeoverElectrochemistryMetalchemistry.chemical_compoundCrystallographychemistryOxidation statevisual_artElectrodevisual_art.visual_art_mediumSpin (physics)ECS Transactions
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Electrochemical capacitance spectroscopy and capacitive relaxation of the changeover process in iron hexacyanoferrate molecular compound

2010

Abstract In this work it was proposed the use electrochemical capacitance spectroscopy (ECS) to evaluate the storage process during changeover in FeHCF compound. The approach is equivalent to electrochemical impedance spectroscopy (EIS) albeit from such analysis it was possible to focus attention on the capacitive and dielectric relaxation instead of the dispersive relaxation related to charge transfer. From such approach it was possible to obtain complementary information on the role played by [Fe 2+ (CN) 6 ] 4− vacancies during the changeover process. It was observed that Fe 3+ (NC) 5 OH − clusters located in these vacancies mediate an electronic and ionic coupled trapping/detrapping proc…

ChemistryGeneral Chemical EngineeringCapacitive sensingElectrochemistryAnalytical chemistryRelaxation (physics)Ionic conductivityIonic bondingDielectricElectrochemistrySpectroscopyDielectric spectroscopyElectrochimica Acta
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