Search results for "Surfaces"

showing 10 items of 2837 documents

Atomic Layer Deposition of Aluminum Oxide on TiO2 and Its Impact on N3 Dye Adsorption from First Principles

2011

The atomic layer deposition of aluminum oxide on an OH-terminated TiO2(101) anatase surface was studied employing density functional theory calculations. The formation of the Al2O3−TiO2 interface during the first atomic layer deposition cycle was modeled by studying the dissociative adsorption of an Al(CH3)3 precursor, followed with a H2O-pulse reaction step that changes the surface termination. Calculations provide evidence for the formation of a discontinuous, atomically rough aluminum oxide layer after the first cycle. To explore the role of the aluminum oxide layer on adsorption of a ruthenium-based N3 dye molecule, various adsorption geometries were investigated. Calculations show that…

inorganic chemicalsAnataseMaterials scienceta114Reaction stepInorganic chemistrychemistry.chemical_elementBlock (periodic table)Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsRutheniumAtomic layer depositionGeneral EnergyAdsorptionchemistryChemical engineeringDensity functional theoryPhysical and Theoretical ChemistryLayer (electronics)ta116Journal of Physical Chemistry C
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Inhibitoren der Korrosion 25(1) - Über die Rolle der Kationen in Neutralsalzen bei der Korrosion von Eisenwerkstoffen in Gegenwart von Sauerstoff

1979

Die Geschwindigkeit des Sauerstoffverbrauchs bei der Korrosion von jeweils 500 mg DAB6-Eisenpulver wird in Abhangigkeit von der Art des Kations in Neutralsalzen (Chloriden) unter Standardbedingungen bestimmt. In Gegenwart von Alkali-, Quartaren Ammonium, Quartaren Phosphonium-und Erdalkalichloriden ist die Geschwindigkeit des Sauerstoffverbrauches vergleichbar gros. Mit Zink-, Cadmium-, Nickel-und Kobaltchloriden wird aber im Bereich von pH5 bis pH7 eine uberraschend grose Verzogerung der Sauerstoffaufnahme beobachtet. Es handelt sich mit hoher Wahrscheinlichkeit um eine Blockade der kathodischen Bezirke in der Eisengrenzflache durch Abscheidung der schwerloslichen basischen Hydroxyde von Z…

inorganic chemicalsCadmiumChemistryMechanical EngineeringMetals and Alloyschemistry.chemical_elementGeneral MedicineZincChlorideOxygenSurfaces Coatings and FilmsNickelchemistry.chemical_compoundMechanics of MaterialsMaterials ChemistrymedicineEnvironmental ChemistryAmmoniumPhosphoniumCobaltmedicine.drugNuclear chemistryMaterials and Corrosion/Werkstoffe und Korrosion
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Iron(iii) oxamato-catalyzed epoxidation of alkenes by dioxygen and pivalaldehyde

1997

A new iron(III)–carbonato monomeric complex of orthophenylenebis( oxamato) (opba) 1 is synthesized, and spectroscopically and structurally characterized; it is a moderately efficient non-heme catalyst for the aerobic epoxidation of alkenes with co-oxidation of pivalaldehyde. Ruiz Garcia, Rafael, Rafael.Ruiz@uv.es ; Fernandez Picot, Isabel, Isabel.Fernandez@uv.es ; Pedro Llinares, Jose Ramon, Jose.R.Pedro@uv.es

inorganic chemicalsDioxygenUNESCO::QUÍMICA::Química inorgánicaUNESCO::QUÍMICAorganic chemicalsIronMetals and AlloysIron ; Dioxygen ; Orthophenylenebis ; Catalyst ; PivalaldehydeGeneral Chemistry:QUÍMICA::Química inorgánica [UNESCO]:QUÍMICA [UNESCO]CatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysischemistry.chemical_compoundMonomerchemistryPolymer chemistryMaterials ChemistryCeramics and Compositesheterocyclic compoundsCatalystOrthophenylenebisPivalaldehyde
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Tetraiodoethynyl resorcinarene cavitands as multivalent halogen bond donors

2014

The first examples of iodoethynyl resorcinarene cavitands as rigid 3D halogen bond (XB) donor molecules are presented. These concave macrocycles form strong, RXB = 0.78–0.83, halogen bonds with dioxane oxygen, pyridine nitrogen and a bromide anion in tetraproropyl ammonium bromide resulting in deep cavity cavitand structures.

inorganic chemicalsHalogen bondChemistryMetals and Alloyschemistry.chemical_elementGeneral ChemistryResorcinarenePhotochemistryOxygenNitrogenCatalysis3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundBromidePolymer chemistryHalogenMaterials ChemistryCeramics and Compositesta116Chemical communications
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Graphitically encapsulated cobalt nanocrystal assemblies

2010

Graphitically encapsulated cobalt nanocrystal assemblies are chemically prepared by one-pot reaction at380 degrees C followed by a reversed etching process to produce porous graphitic structure for revealing their self-assembling nature.

inorganic chemicalsHot TemperatureMaterials sciencefungitechnology industry and agricultureMetals and Alloyschemistry.chemical_elementNanotechnologyCobaltGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMagneticschemistryNanocrystalEtching (microfabrication)Scientific methodMaterials ChemistryCeramics and CompositesNanoparticlesPorosityPorosityCobaltChemical Communications
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Cocrystal trimorphism as a consequence of the orthogonality of halogen- and hydrogen-bonds synthons.

2019

True trimorphic cocrystals, i.e. multi-component molecular crystals of identical composition that exhibit three polymorphic structures, are exceedingly rare and so far no halogen-bonded cocrystal system has been reported to exhibit trimorphism. Here we describe a unique example of a trimorphic cocrystal exhibiting both hydrogen and halogen bonds in which the differences between polymorphs reveal their orthogonality, evident by the apparently independent variation of well-defined hydrogen- and halogen-bonded motifs. peerReviewed

inorganic chemicalsHydrogenchemistry.chemical_element010402 general chemistry01 natural sciencesCocrystalCatalysiskemialliset sidoksetOrthogonalityTrimorphismMaterials Chemistrysupramolekulaarinen kemiavetysidokset010405 organic chemistryHydrogen bondSynthonMetals and Alloysorthogonality halogen bond hydrogen bond cocrystal trimorphismGeneral Chemistrykiteet0104 chemical sciences3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistryHalogenCeramics and CompositesChemical communications (Cambridge, England)
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Effect of air on oxygen p-doped graphene on SiO2

2016

Stability in ambient air or in vacuum-controlled atmosphere of molecular oxygen-induced p-type doping of graphene monolayer on SiO2 substrate on Si is investigated by micro-Raman spectroscopy and atomic force microscopy (AFM). The Raman 2D and G bands spectral positions and amplitude ratio are affected by the permanence in air atmosphere in a time scale of months whereas the vacuum safely maintains the doping effects determined through Raman bands. No morphological effects are induced by the doping and post-doping treatments. A reactivity of ambient molecular gas with stably trapped oxygen is suggested to induce the doping modification. (C) 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

inorganic chemicalsMaterials Chemistry2506 Metals and AlloyElectronic Optical and Magnetic MaterialSettore FIS/01 - Fisica Sperimentaletechnology industry and agricultureSurfaces Coatings and FilmCondensed Matter Physicgraphene dopingCondensed Matter::Materials ScienceCondensed Matter::Strongly Correlated ElectronsSiAFMSiO2Electrical and Electronic Engineeringhuman activitiesRamanSurfaces and Interface
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Production of Phosphorescent Coatings on 6082 Aluminum Using Sr0.95Eu0.02Dy0.03Al2O4-δ Powder and Plasma Electrolytic Oxidation

2019

In this study, a new approach for producing phosphorescent aluminum coatings was studied. Using the plasma electrolytic oxidation (PEO) process, a porous oxide coating was produced on the Al6082 aluminum alloy substrate. Afterwards, activated strontium aluminate (SrAl2O4: Eu2+, Dy3+) powder was filled into the cavities and pores of the PEO coating, which resulted in a surface that exhibits long-lasting luminescence. The structural and optical properties were studied using XRD, SEM, and photoluminescence measurements. It was found that the treatment time affects the morphology of the coating, which influences the amount of strontium aluminate powder that can be incorporated into the coating …

inorganic chemicalsMaterials scienceMorphology (linguistics)Photoluminescencechemistry.chemical_element02 engineering and technologyengineering.material01 natural scienceschemistry.chemical_compoundCoatingPlasma electrolytic oxidation (PEO)Aluminium0103 physical sciencesLuminescent coatings:NATURAL SCIENCES:Physics [Research Subject Categories]Materials Chemistry010302 applied physicsAluminum 6082aluminum 6082Phosphorescencetechnology industry and agricultureStrontium aluminateSurfaces and InterfacesPlasma electrolytic oxidationplasma electrolytic oxidation (PEO)021001 nanoscience & nanotechnologySurfaces Coatings and Filmsphosphorescenceluminescent coatingschemistryChemical engineeringengineering0210 nano-technologyLuminescencePhosphorescenceCoatings
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Optimized bath for electroless deposition of palladium on amorphous alumina membranes

2006

A new bath for the electroless deposition of palladium on anodic alumina (AA) membranes is proposed. It was found that the optimal conditions for the uniform deposition of palladium, with minimal damage to the AA membranes, were under conditions of pH 8.4 and plating times shorter than 30 min. The deposited Pd layer was detected by X-ray diffraction (XRD) and energy dispersive X-ray (EDX) analysis. The morphology of the AA membrane before and after plating was examined by scanning electron microscopy (SEM). EDX analysis revealed that palladium was deposited only on the surfaces of the membrane and Sn ions, coming from the sensitizing bath, were incorporated into the palladium layer. EDTA in…

inorganic chemicalsMaterials scienceScanning electron microscopeInorganic chemistrychemistry.chemical_elementSurfaces and InterfacesGeneral ChemistryCondensed Matter PhysicsSurfaces Coatings and FilmsAmorphous solidMembranechemistryAluminiumPlatingMaterials ChemistryFourier transform infrared spectroscopyElectroless deposition Palladium Dehydrogenation Anodic alumina membranesLayer (electronics)PalladiumSurface and Coatings Technology
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Acetylcholine-responsive cargo release using acetylcholinesterase-capped nanomaterials

2019

[EN] Mesoporous silica nanoparticles capped with acetylcholinesterase, through boronic ester linkages, selectively release an entrapped cargo in the presence of acetylcholine.

inorganic chemicalsNanoparticlemacromolecular substances010402 general chemistry01 natural sciencesCatalysisNanomaterialschemistry.chemical_compoundQUIMICA ORGANICAQUIMICA ANALITICAMaterials ChemistrymedicineBIOQUIMICA Y BIOLOGIA MOLECULAR010405 organic chemistryQUIMICA INORGANICAtechnology industry and agricultureMetals and AlloysGeneral ChemistryMesoporous silicaCombinatorial chemistryAcetylcholinesterase0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialsstomatognathic diseaseschemistryCeramics and CompositesAcetylcholinemedicine.drug
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