Search results for "interfaces"

showing 10 items of 1258 documents

First heavy ion beam tests with a superconducting multigap CH cavity

2018

Physical review accelerators and beams 21(2), 020102 (2018). doi:10.1103/PhysRevAccelBeams.21.020102

SuperconductivityPhysicsNuclear and High Energy PhysicsPhysics and Astronomy (miscellaneous)Mass-to-charge ratio010308 nuclear & particles physicsSurfaces and InterfacesInjector53001 natural sciencesLinear particle acceleratorlaw.inventionIonNuclear physicsAccelerationlaw0103 physical scienceslcsh:QC770-798Physics::Accelerator PhysicsContinuous wavelcsh:Nuclear and particle physics. Atomic energy. Radioactivityddc:530010306 general physicsBeam (structure)Physical Review Accelerators and Beams
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Critical Micelle Density for the Self-Assembly of Block Copolymer Surfactants in Supercritical Carbon Dioxide

1999

The parameters which influence the self-assembly of molecules in solution include the temperature and solvent quality, and this study illustrates the use of these variables to regulate the degree of association of block copolymer amphiphiles in highly compressible supercritical carbon dioxide. Small-angle neutron scattering (SANS) has been used to examine the association behavior of a block copolymer containing a CO2-phobic moiety, poly(vinyl acetate), and a CO2-philic block, poly(1,1-dihydroperfluoro-octylacrylate). By adjustment of the density of the medium through pressure and temperature profiling, the self-assembly can be reversibly controlled from unimers to core−shell spherical micel…

Supercritical carbon dioxideMaterials scienceSurfaces and InterfacesNeutron scatteringCondensed Matter PhysicsMicelleSupercritical fluidSolventchemistry.chemical_compoundChemical engineeringchemistryAmphiphilePolymer chemistryElectrochemistryCopolymerVinyl acetateGeneral Materials ScienceSpectroscopyLangmuir
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Growth of polycrystalline nickel hydroxide films from aqueous solution. Solution chemistry, deposition methods, film morphology and texture

2014

Abstract Deposition of functional ceramic films on different substrates by using soft aqueous solution processing can represent a cheap, low- energy and environmental friendly alternative to other film technologies. In this study β-Ni(OH)2 polycrystalline films were grown on polytetrafluoroethylene, NiO, glass, copper, and Y:ZrO2 substrates from Ni2 +–NH4OH aqueous solutions. A careful control of solution supersaturation was essential to induce heterogeneous nucleation on the substrate and film growth. This was realized through the gradual decomposition of the nickel amino complexes Ni(NH3)n2 + using two different methods. Thermodynamic modeling of the Ni–NH4OH–H2O system was used to provid…

SupersaturationMaterials scienceAqueous solutionNickel hydroxideInorganic chemistrySupersaturated solutionMetals and AlloysOxideNucleationSurfaces and InterfacesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsFilm morphologychemistry.chemical_compoundchemistryMaterials ChemistryHydroxideDeposition (phase transition)CrystalliteTexture (crystalline)Nucleation Growth from solutionFilm texture
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Morphology and electronic structure of bcc Co(110) and fcc/hcp Co(111) on Fe(110) investigated by STM and STS

2009

Abstract We report on the growth of ultrathin epitaxial Co films on Fe(1 1 0) examined by scanning tunneling microscopy and spectroscopy (STM and STS). At room temperature Co forms pseudomorphic, ideally ordered body-centered cubic (bcc) layers for the first two monolayers as confirmed by atomically resolved STM images. This is in contrast to the related case of Co/Cr(1 1 0) where a superstructure occurs in the second layer. The third monolayer forms a close-packed structure and causes a transformation of the buried second monolayer into a close-packed structure. The Fe(1 1 0) substrate strongly influences the electronic structure of the first Co monolayer as concluded from the dI / dU spec…

SuperstructureChemistryScanning tunneling spectroscopySurfaces and InterfacesElectronic structureSubstrate (electronics)Condensed Matter PhysicsEpitaxySurfaces Coatings and Filmslaw.inventionCrystallographyTransition metallawMonolayerMaterials ChemistryScanning tunneling microscopeSurface Science
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Electrochemical impedance spectroscopy of polyelectrolyte multilayer modified gold electrodes: influence of supporting electrolyte and temperature.

2005

Electrochemical impedance spectroscopy and cyclic voltammetry are employed to characterize poly(styrenesulfonate)/poly(allylamine hydrochloride) multilayers assembled onto cysteamine-modified gold surfaces. The influence of the supporting electrolyte and temperature on the impedance response is studied because of both its practical interest and the need to test further the capillary membrane model recently developed by Barreira et al. [J. Phys. Chem. B 2004, 108, 17973]. The results obtained are interpreted quite satisfactorily in terms of this model, thus providing additional support to its usefulness for the description of ionic transport through polyelectrolyte multilayers. It is observe…

Supporting electrolyteCysteamineAnalytical chemistryActivation energyElectrolyteBiosensing TechniquesElectrochemistrysymbols.namesakeElectrolytesElectric ImpedanceElectrochemistryPolyaminesGeneral Materials ScienceElectrodesSpectroscopyArrhenius equationIonsModels StatisticalChemistrySpectrum AnalysisTemperatureSurfaces and InterfacesCondensed Matter PhysicsPolyelectrolyteDielectric spectroscopysymbolsPolystyrenesGoldCyclic voltammetryLangmuir : the ACS journal of surfaces and colloids
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Geminal Imidazolium Salts: A new Class of Gelators

2012

The gelling behavior of some geminal diimidazolium salts was investigated in solvents differing in polarity and hydrogen bond donor ability. The used salts, namely the 3,3'-di-n-decyl-1,1'(1,4-phenylenedimethylene)diimidazolium dibromide [p-Xyl-(decim)(2)][Br](2) (1), the 3,3'-di-n-dodecyl-1,1'(1,4-phenylenedimethylene)diimidazolium dibromide [p-Xyl-(dodecim)(2)][Br](2) (2), and the 3,3'-di-n-dodecyl-1,1'(1,4-phenylenedimethylene)diimidazolium ditetrafluoroborate [p-Xyl-(dodecim)(2)][BF(4)](2) (3), differ in the alkyl chain length and in the anion properties, such as size, shape, and coordination ability. In all cases in which gelation process was observed, the obtained gels were characteri…

Supramolecular chemistrychemistry.chemical_compoundBromidePolymer chemistryElectrochemistryMoleculeOrganic chemistryGeneral Materials ScienceSpectroscopyAlkylchemistry.chemical_classificationMolecular StructureGeminalHydrogen bondChemistryImidazolesHydrogen BondingSurfaces and InterfacesSettore CHIM/06 - Chimica OrganicaCondensed Matter PhysicsResonance (chemistry)Geminal imidazolium salts Low molecular weight gelator OrganogelThermodynamicsSaltsChemical stabilityGelsOrganogels Hydrogels imidazolium salts
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An empirical model for free surface energy of strained solids at different temperature regimes.

2006

Abstract We have developed an empirical formulation, based on the elastic theory, to calculate the variation of the surface free energy when a crystal is strained in the elastic regime. The model permits to obtain the variation of the surface energy at different strains and temperatures when are known the thermal dependence on the bulk and surface elastic constants. Molecular dynamics (MD) simulations were performed using the three low index surfaces of Al, to validate the accuracy of the model. The comparison between the empirical model and the MD simulations shows a good agreement for temperatures ranging between 0 and 900 K, and for deformation between −2% and 2%.

Surface (mathematics)ChemistryGeneral Physics and AstronomyThermodynamicsmodelingSurfaces and InterfacesGeneral ChemistryMolecular dynamicsCondensed Matter PhysicsSurface energySurfaces Coatings and FilmsStrain energyCrystalMolecular dynamicsPACS: 68.35.Md; 31.15.Qgsurface energyFree surface[ CHIM.MATE ] Chemical Sciences/Material chemistryThermalStatistical physicsDeformation (engineering)
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Atomistic simulation of SrTiO3 and BaTiO3 (110) surface relaxations

2000

Abstract The (110) surface relaxations were calculated for SrTiO 3 and BaTiO 3 perovskites in a cubic phase. Using a shell model, the positions of atoms in 16 near- surface layers placed atop a slab of rigid ions are calculated. The strong surface rumpling and induced surface dipole moments perpendicular to the surface are predicted for both the O-terminated and TiO-terminated surfaces.

Surface (mathematics)ChemistrySHELL modelMetals and AlloysMineralogySurfaces and InterfacesMolecular physicsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonCondensed Matter::Materials Sciencechemistry.chemical_compoundDipolePhase (matter)Materials ChemistrySlabStrontium titanatePerpendicularThin Solid Films
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ATOMISTIC CALCULATIONS OF (110) SURFACE RELAXATION FOR PEROVSKITE TITANATES

1999

Using a shell model, for the first time the (110) surface relaxations are calculated for SrTiO 3 and BaTiO 3 perovskites. The positions of atoms in 16 near-surface layers placed atop a slab of rigid ions are calculated. Strong surface rumpling and surface-induced dipole moments perpendicular to the surface are predicted for both the O-terminated and Ti-terminated surfaces.

Surface (mathematics)Condensed matter physicsChemistrySHELL modelRelaxation (NMR)Surfaces and InterfacesCondensed Matter PhysicsSurfaces Coatings and FilmsIonDipoleMaterials ChemistrySlabPerpendicularPerovskite (structure)Surface Review and Letters
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Quenched molecular dynamics studies on the extraction energy of aluminum atoms

2007

The extraction energy of an aluminum atom is calculated at 0 K as a function of coordination number and defect depth for three surface orientations [(100), (110) and (111)]. For each orientation, atoms are selected and extracted one by one. A linear relationship is obtained between the extraction energy of surface atoms and their coordination numbers (with slight variations due to the geometrical configuration of the atoms). However, the study of the influence of the defect depth on the extraction energy highlights the role played by intrinsic stress on the extraction energy. Copyright © 2008 John Wiley & Sons, Ltd.

Surface (mathematics)Coordination numberchemistry.chemical_element02 engineering and technology01 natural sciencesMolecular physicsStress (mechanics)Molecular dynamicsAluminiumVacancy defect0103 physical sciencesAtomMaterials ChemistryPhysics::Atomic and Molecular Clusters010306 general physicsExtraction (chemistry)Surfaces and InterfacesGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsSurfaces Coatings and Filmschemistry[ CHIM.MATE ] Chemical Sciences/Material chemistryAtomic physics0210 nano-technology
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