Search results for " electrochemistry"

showing 10 items of 67 documents

How far are we from the valorization of waste-CO2 to formic acid via electrochemical routes for the applicative scale?

To date, the decarbonization of the world economy and storage and production of energy from alternative C-based sources is considered a relevant topic. The electrochemical conversion of CO2 has been widely investigated since the 1870s as a promising strategy to convert waste-CO2 into value-added chemicals [1,2]. Recently, it was highlighted that, among the several emerging technologies for CO2 conversion to value-added products on an applicative scale, electrochemical technologies are the closest to commercialization due to the numerous start-ups and established companies being invested in this area (e.g., Opus-12, Dioxide Material, and Carbon Recycling International) [3]. These technologie…

CO2 conversion electrochemistry Formic acid pressure GDESettore ING-IND/27 - Chimica Industriale E Tecnologica
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Sensor Properties of Pristine and Functionalized Carbon Nanohorns

2016

Nanodispersions of pristine single-wall carbon nanohorns (i.e., p-SWCNHs) and oxidized-SWCNHs (i.e.; o-SWCNHs) were used to modify screen printed electrode (SPE). p-SWCNHs and o-SWCNHs were fully characterized by using several analytical techniques, as: HR-TEM (High Resolution-Transmission Electron Microscopy), FE-SEM/EDX (Field Emission-Scanning Electron Microscopy/Energy Dispersive X-ray Analysis), Raman spectroscopy, thermogravimetric analysis, differential thermal analysis (DTA), and the Brunauer-Emmett-Teller (BET) method. The chemically modified SPEs were also characterized with Cyclic Voltammetry (CV), using several different electro-active targets. In all cases, p-SWCNHs showed bett…

Carbon NanohornThermogravimetric analysisScreen Printed ElectrodesMaterials scienceAnalytical chemistrychemistry.chemical_element02 engineering and technologyGlassy carbon010402 general chemistryElectrochemistry01 natural sciencesCarbon NanohornsAnalytical Chemistrysymbols.namesakeDifferential thermal analysisElectrochemistrySettore CHIM/01 - Chimica AnaliticaSingle-WallCarbon Nanohorns; Screen Printed Electrodes; Single-Wall; Analytical Chemistry; ElectrochemistryScreen Printed Electrode021001 nanoscience & nanotechnology0104 chemical scienceschemistryElectrodesymbolsCyclic voltammetry0210 nano-technologyRaman spectroscopyCarbonElectroanalysis
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Substituent effect on the redox potential of substituted (aryl)(2-nitrobenzo[ b ]thiophen-3-yl)amines

2001

Abstract The electronic effect of some meta- or para-substituents on the reduction of the title compounds has been investigated. The reversible reduction potential values of these compounds have been evaluated by cyclic voltammetry at a mercury electrode in 0.1 M tetraethylammoniumtetrafluoroborate, dimethylsulfoxide solutions. The substituent effect depends on both its nature and its position. The reduction potential values of the derivatives studied have been correlated with the Hammett substituent constants.

ChemistryArylOrganic ChemistrySubstituentDropping mercury electrodeBiochemistryRedoxMedicinal chemistrychemistry.chemical_compoundorganic electrochemistry substituents effect on thermodynamics redox processesDrug DiscoveryElectronic effectOrganic chemistryCyclic voltammetryTetrahedron
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Electrolyte-driven electrochemical amplification by poly(thienylacetylene) encapsulated within Zeolite Y

2006

Electrochemical oxidation and reduction of poly(thienylacetylene) encapsulated inside zeolite Y (PTA@Y) exhibit with large anodic and cathodic doping currents with a significant reversibility. Thienyl groups lower the redox potential of polyacetylene chain whereas encapsulation stabilizes the resulting charged radical species blocking undesired post electron-transfer cross-link reactions. Size-exclusion effects associated produces an electrolyte-dependent amplification of currents recorded at PTA@Y-modified electrodes for electrochemical processes involving selected substrates in solution, namely, dinitrobiphenyl and benzidine. Keywords: Poly(thienylacetylene), Zeolite Y, Electrochemistry, …

ChemistryElectrolyteElectrochemistryElectrocatalystPhotochemistryRedoxBenzidinelcsh:ChemistryElectron transferchemistry.chemical_compoundPolyacetylenelcsh:Industrial electrochemistrylcsh:QD1-999ElectrodeElectrochemistryOrganic chemistrylcsh:TP250-261Electrochemistry Communications
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Electrocatalysis of the oxidation of methylenedioxyamphetamines at electrodes modified with cerium-doped zirconias

2004

The catalytic effect of monoclinic and tetragonal cerium-doped zirconias (m-CexZr1−xO2 and t-CexZr1−xO2, 0<x<0.10, respectively), prepared from gel precursors, on the oxidation of methylenedioxyamphetamine (MDA) and methylenedioxymetamphetamine (MDMA) at pH 7.0 has been studied. Upon attachment of synthetic specimens to polymer film electrodes, an oxidation peak near to +1.05 V vs AgCl/Ag appears that is unaffected by chloride ions and common interfering compounds, namely, dopamine, norepinephrine and ascorbic acid. The catalytic effect appears to be strongly influenced by crystallinity of specimens and coordination of cerium, increasing from the amorphous starting material to t-CexZr1−xO2 …

ChemistryInorganic chemistryDopingchemistry.chemical_elementElectrocatalystElectrochemistryCatalysislcsh:ChemistryTetragonal crystal systemCeriumlcsh:Industrial electrochemistrylcsh:QD1-999ElectrodeElectrochemistryMonoclinic crystal systemlcsh:TP250-261Electrochemistry Communications
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Electrochemistry nanometric patterning of MOF particles: Anisotropic metal electrodeposition in Cu/MOF

2006

Abstract Electrodeposition of copper from Cu/MOF immersed into acetate buffer produces a quasi-periodic series of 10–20 nm sized laminae sandwiched within the pristine MOF lattice as monitored by voltammetry of microparticles/atomic force microscopy. This anisotropic patterning can be qualitatively described in terms of a highly orientation-dependent diffusion of electrons and charge-balancing electrolyte counterions in the MOF network.

ChemistryInorganic chemistrychemistry.chemical_elementElectrolyteBuffer solutionElectrochemistryCopperlcsh:Chemistrychemistry.chemical_compoundlcsh:Industrial electrochemistrylcsh:QD1-999Transition metalTransmission electron microscopyElectrochemistryMetal-organic frameworkVoltammetrylcsh:TP250-261Electrochemistry Communications
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Mass/charge balance as a tool to estimate dimensional change in polypyrrole-based actuators

2006

The deconvolution of the voltammograms of polypyrrole electrochemistry has proved to be possible through the electrochemical quartz crystal microbalance data using the F(dm/dQ) function. This deconvolution allows the evolution of the thickness of the polypyrrole films during their redox processes to be estimated and therefore, the mechanical contraction/decontraction of this polymer as a function of the ionic exchange processes can be evaluated. Keywords: Polypyrrole, EQCM, Thickness change

Conductive polymerchemistry.chemical_classificationPolypyrrole; EQCM; Thickness changeChemistryAnalytical chemistryIonic bondingPolymerQuartz crystal microbalanceElectrochemistryPolypyrrolelcsh:Chemistrychemistry.chemical_compoundlcsh:Industrial electrochemistrylcsh:QD1-999Chemical physicsMass transferElectrochemistry[CHIM]Chemical SciencesDeconvolutionlcsh:TP250-261
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Azolium and acetate ions in DMF: Formation of free N-heterocyclic carbene. A voltammetric analysis

2016

In order to reveal the possible formation of free N-heterocyclic carbene (NHC) in DMF-azolium and acetate solutions, the proton exchange equilibrium between azolium cations and CH3COO− was investigated (by cyclic voltammetry) by adding CH3COOH or tetrabutylammonium acetate to DMF solutions of imidazolium or thiazolium salts of different acidity.The voltammetric analysis confirms that the deprotonation of the azolium cation by CH3COO− (with the formation of free NHC) is significant in the case of the more acidic thiazolium cations, while it is not effective with the less acidic imidazolium ones.Accordingly, the NHC-catalyzed benzoin condensation was carried out in DMF solutions of azolium sa…

Cyclic voltammetryNHCInorganic chemistryTetrabutylammonium acetate010402 general chemistryAcetic acid01 natural sciencesMedicinal chemistryIonlcsh:ChemistryBenzaldehydeAcetic acidchemistry.chemical_compoundDeprotonationBenzoinElectrochemistryBenzoin condensationBenzoin condensation010405 organic chemistryChemistry0104 chemical sciencesAzolium saltslcsh:Industrial electrochemistrylcsh:QD1-999Acetic acid; Azolium salts; Benzoin condensation; Cyclic voltammetry; NHC; Tetrabutylammonium acetate; ElectrochemistryAzolium saltCyclic voltammetryCarbenelcsh:TP250-261
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eta1-Allypalladium complexes with tridentate PNP’ ligand for the assembly of modified Screen Printed Electrodes: an electrochemical study.

2015

Specific Pd-based organometallic complex, in particular the [Pd(η1-CH2–CH=CH2)(P–N–P’)]BF4 was used for the assembly of chemically modified Screen Printed Electrodes (SPEs) and their electrochemical reactivity was also investigated. For this purpose potassium ferricyanide, hexaammineruthenium(III) chloride, sodium hexachloroiridate-(III) hydrate, ascorbic acid (AA), uric acid (UA), acetaminophen (Ac), guanine (G) and adenine (A) were used to study the electron-transfer processes, which occurred at modified SPEs, fabricated by using the [Pd(η1-CH2–CH=CH2)(P–N–P’)]BF4, applying the drop casting procedure. Interesting results were obtained in the case of the guanine (G) quantitative detection,…

Detection limitElectrocatalysis towards guanine/GP-N-P complexesGuanineAnalytical chemistryPd center dot P-N-P complexesElectrochemistryAscorbic acidHeterogeneous electron-transfer kinetic constantsAnalytical Chemistry: Pdchemistry.chemical_compoundPotassium ferricyanidechemistrychemically modified SPEsElectrodeElectrochemistryReactivity (chemistry)Settore CHIM/01 - Chimica Analitica: Pd; P-N-P complexes; chemically modified SPEs; Electrochemistry; Heterogeneous electron-transfer kinetic constants electro-catalysis towards nucleic acidsHydrateNuclear chemistryelectro-catalysis towards nucleic acids
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Growth and characterization of horizontally suspended CNTs across TiN electrode gaps.

2010

A technique is proposed to grow horizontal carbon nanotubes (CNTs) bridging metal electrodes and to assess their electrical properties. A test structure was utilized that allows for selective electrochemical sidewall catalyst placement. The selectivity of the technique is based on the connection of the desired metal electrodes to the silicon substrate where the potential for electrochemical deposition was applied. Control over the Ni catalyst size (15-30 nm) and density (up to 3 x 10(11) particles cm(-2)) is demonstrated. Horizontal CNTs with controlled diameter and density were obtained by CVD growth perpendicular to the sidewalls of patterned TiN electrode structures. Electrode gaps with …

FabricationMaterials scienceSiliconScanning electron microscopeElectrodeHeterogeneous catalysis at surfacechemistry.chemical_elementBioengineeringNanotechnologyChemical vapor depositionCarbon nanotubeSettore ING-INF/01 - Elettronicalaw.inventionlawGeneral Materials ScienceElectrical and Electronic EngineeringOhmic contactbusiness.industryMechanical EngineeringSurface and interface chemistryGeneral ChemistryNanostructured materials in electrochemistryNanotubechemistryMechanics of MaterialsElectrodeOptoelectronicsTinbusinessScanning electron microscopyNanotechnology
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