Search results for "Surfaces"

showing 10 items of 2837 documents

Oscillatory Changes of the Heterogeneous Reactive Layer Detected with the Motional Resistance during the Galvanostatic Deposition of Copper in Sulfur…

2015

Metallic copper was galvanostatically deposited on quartz|gold resonant electrodes by applying a constant current in a 0.5 M CuSO4/0.1 M H2SO4 aqueous solution. Galvanostatic copper deposition is one of the best methodologies to calibrate the electrochemical quartz crystal microbalances (EQCM), a gravimetric sensor to evaluate changes in mass during the electrochemical reactions through the Sauerbrey equation. The simultaneous measurement of mass, current density, and motional resistance by an EQCM with motional resistance monitoring allows us to characterize the processes occurring on the electrode surface and at the interfacial regions with unprecedented detail. During the galvanostatic c…

Auxiliary electrodeWorking electrodeInorganic chemistryAnalytical chemistrychemistry.chemical_elementElectrochemistryMotionSauerbrey equationElectrochemistryDeposition (phase transition)General Materials ScienceElectrodesSpectroscopyElectric ConductivitySurfaces and InterfacesHydrogen PeroxideSulfuric AcidsCondensed Matter PhysicsCopperOxygenSolutionschemistryElectrodeCalibrationQuartz Crystal Microbalance TechniquesLayer (electronics)CopperLangmuir : the ACS journal of surfaces and colloids
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Kinetics of Zn2+ complexation by a ditopic phenanthroline-azamacrocyclic scorpiand-like receptor.

2012

Coordination of Zn(2+) to a ditopic phenanthroline-macrocycle receptor takes place in three steps, the first one being the coordination to the phenanthroline, followed by the slow movement of the metal to the polyamine macrocycle and a final re-arrangement to coordinate the pendent arm.

Aza CompoundsStereochemistryPhenanthrolineKineticsMetals and AlloysGeneral ChemistryHydrogen-Ion ConcentrationCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMetalchemistry.chemical_compoundKineticsZincchemistryCoordination Complexesvisual_artPolymer chemistryMaterials ChemistryCeramics and Compositesvisual_art.visual_art_mediumSlow MovementPolyamineReceptorPhenanthrolinesChemical communications (Cambridge, England)
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The azido ligand: a useful tool in designing chain compounds exhibiting alternating ferro- and antiferro-magnetic interactions

1997

A one-pot reaction of NiII 1, CoII 2, FeII 3 and MnII 4 with 2,2A-bipyridine (bipy) and azide in water leads to [M(bipy)(N3)2]n chains where the metal ion is alternatively bridged by double end-on (EO) and end-to-end (EE) azido bridges; theoretical analysis of the variable-temperature magnetic susceptibility data of 1 and 4 reveals the occurrence of intrachain alternating ferro- (through EO) and antiferro-magnetic (through EE) interactions. Julve Olcina, Miguel, Miguel.Julve@uv.es ; Lloret Pastor, Francisco, Francisco.Lloret@uv.es ; Clemente Juan, Juan Modesto, Juan.M.Clemente@uv.es

Azido ligand ; Ferro-magnetic ; Antiferro-magnetic ; BipyrineStereochemistryUNESCO::QUÍMICABipyrine:QUÍMICA [UNESCO]CatalysisMetalchemistry.chemical_compoundChain (algebraic topology)Ferro-magneticMaterials ChemistryChemistryLigandUNESCO::QUÍMICA::Química inorgánicaMetals and AlloysAzido ligandGeneral Chemistry:QUÍMICA::Química inorgánica [UNESCO]Magnetic susceptibilitySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyvisual_artAntiferro-magneticCeramics and Compositesvisual_art.visual_art_mediumAzide
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Systematic trends in (0 0 1) surface ab initio calculations of ABO 3 perovskites

2018

This work was supported by the Latvian Council of Science Grant No. 374/2012 and the Latvian National Research Program IMIS2. Many stimulating discussions with D. Vanderbilt, K.M. Rabe, M. Rohlfing, E. Heifets, J. Maier, G. Borstel and E.A. Kotomin are greatly acknowledged.

B3LYPBand gapABO3 perovskitesPopulation02 engineering and technology01 natural scienceslcsh:ChemistryCrystalAb initio quantum chemistry methodsComputational chemistry0103 physical sciences:NATURAL SCIENCES:Physics [Research Subject Categories]Surface layer010306 general physicseducationPerovskite (structure)(0 0 1) surfaceseducation.field_of_studyCondensed matter physicsChemistryRelaxation (NMR)General Chemistry021001 nanoscience & nanotechnologyB3PWlcsh:QD1-999Chemical bondAb initio calculations0210 nano-technologyJournal of Saudi Chemical Society
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Electron Transfer from Organic Aminophenyl Acid Sensitizers to Titanium Dioxide Nanoparticle Films

2009

Electron transfer from three conjugated amino-phenyl acid dyes to titanium and aluminum oxide nanocrystalline films was studied by using transient absorption spectroscopy with sub 20 fs time-resolution over the visible spectral region. All the dyes attached to TiO2 showed long-lived ground state bleach signals indicative of formation of new species. Global analysis of the transient kinetics of the dyes on TiO2 revealed stimulated emission decays of about 40 fs and less than 300 fs assigned to electron injection. The same dyes on Al2O3 substrates displayed long stimulated emission decays (ns) suggesting that electron transfer is blocked in this high band gap semiconductor. For two of the dye…

Band gapConjugated systemPhotochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundElectron transferGeneral EnergychemistryTitanium dioxideUltrafast laser spectroscopyDensity functional theoryStimulated emissionPhysical and Theoretical ChemistrySpectroscopyThe Journal of Physical Chemistry C
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Acid-Base Properties of 2:1 Clays. I. Modeling the Role of Electrostatics

2010

We present a theoretical investigation of the titratable charge of clays with various structural charge (sigma(b)): pyrophyllite (sigma(b) = 0 e x nm(-2)), montmorillonite (sigma(b) = -0.7 e x nm(-2)) and illite (sigma(b) = -1.2 e x nm(-2)). The calculations were carried out using a Monte Carlo method in the Grand Canonical ensemble and in the framework of the primitive model. The clay particle was modeled as a perfect hexagonal platelet, with an "ideal" crystal structure. The only fitting parameters used are the intrinsic equilibrium constants (pK(0)) for the protonation/deprotonation reactions of the broken-bond sites on the lateral faces of the clay particles, silanol, =SiO(-) + H(+) --=…

Base (chemistry)Mineralogy02 engineering and technologyengineering.material010402 general chemistry01 natural scienceschemistry.chemical_compoundElectrochemistryGeneral Materials ScienceCharging ProcessSpectroscopyPyrophyllitechemistry.chemical_classificationSurfaces and Interfaces021001 nanoscience & nanotechnologyCondensed Matter PhysicsElectrostatics0104 chemical sciences[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]MontmorillonitechemistryChemical engineeringvisual_artIlliteengineeringvisual_art.visual_art_mediumClay[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technology
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Acid–Base Properties and Surface Charge Distribution of the Water-Soluble Au102(pMBA)44 Nanocluster

2016

The pKa of the p-mercaptobenzoic acid (pMBA) ligands in the Au102(pMBA)44 nanocluster was measured by using acid–base and IR titration. The observed macroscopic pKa = 6.18 ± 0.05 is significantly more basic than that of free pMBA (pKa = 4.16), and the protonation behavior is anticooperative according to the Hill coefficient n = 0.64 ± 0.04. The cluster is truly water-soluble when more than 22 and insoluble when fewer than 7 ligands are in the deprotonated state. In order to obtain more insight into the anticooperative character, the cluster was modeled at pH ∼6.2 using constant pH molecular dynamics simulations. The pKa values of the individual pMBAs are in the range of 5.18–7.58, depending…

Base (chemistry)acid–base propertiesInorganic chemistryProtonation02 engineering and technology010402 general chemistry01 natural sciencescharge distributionMolecular dynamicsDeprotonationCluster (physics)Surface chargePhysical and Theoretical Chemistryta116chemistry.chemical_classificationChemistryCharge density021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyPhysical chemistryTitration0210 nano-technologygold nanoclustersJournal of Physical Chemistry C
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Carbon-Coated Anatase TiO2Nanotubes for Li- and Na-Ion Anodes

2014

aInstitute of Physical Chemistry and MEET Battery Research Centre, University of Muenster, 48149 Muenster, Germany bHelmholtz-Institute Ulm (HIU), Electrochemistry I, 89081 Ulm, Germany cKarlsruher Institute of Technology (KIT), 76021 Karlsruhe, Germany dInstitute for Organic Chemistry, University of Mainz, 55128 Mainz, Germany eGraduate School Materials Science in Mainz, 55128 Mainz, Germany fInstitute for Inorganic and Analytical Chemistry, University of Mainz, 55128 Mainz, Germany gMax Planck Institute for Polymer Research, 55128 Mainz, Germany

Battery (electricity)AnataseMaterials scienceRenewable Energy Sustainability and the EnvironmentCondensed Matter PhysicsElectrochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAnodeChemical engineeringResearch centreMaterials ChemistryElectrochemistryCarbon coatingJournal of The Electrochemical Society
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Composite polymer electrolytes with improved lithium metal electrode interfacial properties: II. Application in rechargeable batteries

1998

The application of a liquid-free, ceramic-added composite polymer electrolyte in a Li/LiMn{sub 2}O{sub 4} rechargeable battery is presented and discussed. As expected by the high stability of the electrolyte toward the lithium metal anode, the battery has promising characteristics in terms of reliability and cyclability.

Battery (electricity)Materials scienceRenewable Energy Sustainability and the EnvironmentInorganic chemistryElectrolyteCondensed Matter PhysicsLithium aluminateEnergy storageSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAnodechemistry.chemical_compoundchemistryChemical engineeringElectrodeMaterials ChemistryElectrochemistryFast ion conductorTrifluoromethanesulfonate
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Atomic Layer Deposition of Spinel Lithium Manganese Oxide by Film-Body-Controlled Lithium Incorporation for Thin-Film Lithium-Ion Batteries

2013

Lithium manganese oxide spinels are promising candidate materials for thin-film lithium-ion batteries owing to their high voltage, high specific capacity for storage of electrochemical energy, and minimal structural changes during battery operation. Atomic layer deposition (ALD) offers many benefits for preparing all-solid-state thin-film batteries, including excellent conformity and thickness control of the films. Yet, the number of available lithium-containing electrode materials obtained by ALD is limited. In this article, we demonstrate the ALD of lithium manganese oxide, LixMn2O4, from Mn(thd)3, Li(thd), and ozone. Films were polycrystalline in their as-deposited state and contained le…

Battery (electricity)Materials scienceta114Lithium vanadium phosphate batterySpinelInorganic chemistrychemistry.chemical_elementengineering.materialElectrochemical energy conversionSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAtomic layer depositionGeneral EnergychemistryImpurityengineeringLithiumCrystallitePhysical and Theoretical ChemistryThe Journal of Physical Chemistry C
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