Search results for "nucleation"

showing 10 items of 364 documents

Atomic layer deposition of Ru films from bis(2,5-dimethylpyrrolyl)ruthenium and oxygen

2012

Abstract Ru thin films were grown on hydrogen terminated Si, SiO 2 , Al 2 O 3 , HfO 2 , and TiO 2 surfaces by atomic layer deposition from bis(2,5-dimethylpyrrolyl)ruthenium precursor and oxygen. The 4–20 nm thick films on these surfaces consisted of nanocrystalline hexagonal metallic ruthenium, regardless of the deposition temperature. At the lowest temperatures examined, 250–255 °C, the growth of the Ru films was favored on silicon, compared to the growth on Al 2 O 3 , TiO 2 and HfO 2 . At higher temperatures the nucleation and growth of Ru became enhanced in particular on HfO 2 , compared to the process on silicon. At 320–325 °C, no growth occurred on Si–H and SiO 2 -covered silicon. Res…

Materials scienceSiliconHydrogenNucleationchemistry.chemical_elementNanotechnology02 engineering and technology01 natural sciencesMetalAtomic layer deposition0103 physical sciencesMaterials ChemistryThin filmta116010302 applied physicsta114Metals and AlloysSurfaces and Interfaces021001 nanoscience & nanotechnologyNanocrystalline materialSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsRutheniumchemistryChemical engineeringvisual_artvisual_art.visual_art_medium0210 nano-technologyThin Solid Films
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Atomic Layer Deposition of Ruthenium Films from (Ethylcyclopentadienyl)(pyrrolyl)ruthenium and Oxygen

2011

Ru films were grown by atomic layer deposition in the temperature range of 275―350°C using (ethylcyclopentadienyl)(pyrrolyl)ruthenium and air or oxygen as precursors on HF-etched Si, SiO 2 , ZrO 2 , and TiN substrates. Conformal growth was examined on three-dimensional silicon substrates with 20:1 aspect ratio. ZrO 2 promoted the nucleation of Ru most efficiently compared to other substrates, but the films roughened quickly on ZrO 2 with increasing film thickness. The minimum number of cycles required to form continuous and conductive metal layers could be decreased by increasing the length of the oxygen pulse. In order to obtain well-conducting Ru films growth to thicknesses of at least 8―…

Materials scienceSiliconInorganic chemistryAnalytical chemistryNucleationchemistry.chemical_element02 engineering and technology01 natural sciencesOxygenMetalAtomic layer deposition0103 physical sciencesMaterials ChemistryElectrochemistryta116010302 applied physicsta114Renewable Energy Sustainability and the EnvironmentAtmospheric temperature range021001 nanoscience & nanotechnologyCondensed Matter PhysicsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsRutheniumchemistryvisual_artvisual_art.visual_art_medium0210 nano-technologyTinJournal of The Electrochemical Society
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Effects of partial self-ordering of Si dots formed by chemical vapor deposition on the threshold voltage window distribution of Si nanocrystal memori…

2006

We study the role that the denuded zone around Si nanocrystals obtained by chemical vapor deposition plays on the fluctuations of the dot surface coverage. In fact, the capture mechanism of the silicon adatoms in the proximity of existing dots restricts the number of possible nucleation sites, the final dot size, and the dot position, thus driving the process toward partial self-order. We numerically evaluate the relative dispersion of surface coverage for several gate areas and compare the results to the fully random case. The coverage dispersion is related to the fluctuations from bit to bit of the threshold voltage window (Δ Vth) distribution of nanocrystal memories. The evaluations, com…

Materials scienceSiliconQuantum dotsbusiness.industryNucleationGeneral Physics and Astronomychemistry.chemical_elementWindow (computing)NanotechnologyChemical vapor depositionCondensed Matter::Mesoscopic Systems and Quantum Hall EffectSettore ING-INF/01 - Elettronicanon volatile memoriesSettore FIS/03 - Fisica Della Materiachemical vapor depositionThreshold voltageDistribution (mathematics)chemistryNanocrystalnanoelectronic devicesscaling lawsDispersion (optics)OptoelectronicsbusinessJournal of Applied Physics
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Au/CeO2-SBA-15 catalysts for CO oxidation: Effect of ceria loading on physic-chemical properties and catalytic performances

2012

In this work gold catalysts supported over SBA-15 with different CeO 2 loadings (5-30 wt%) were prepared, characterized by N 2 physisorption analyses, SAXS, XRD, STEM and XPS techniques and their catalytic performances were evaluated in the CO oxidation, chosen as reaction test. Over a selected catalyst, Au/CeO 2(20 wt%)-SBA-15, the effect of CO 2 and of the mixture (CO 2 + H 2O) on the CO conversion to CO 2 was also evaluated. Characterizations by SAXS, XRD, STEM and XPS were carried out on selected spent catalysts after CO oxidation. The results were discussed in terms of relationship between morphological, structural, electronic and catalytic properties as a function of the ceria loading…

Materials scienceSmall-angle X-ray scatteringOxideNucleationSinteringNanotechnologyGeneral ChemistryCatalysisCatalysischemistry.chemical_compoundAu CeO2 SBA-15 catalysts CO oxidationchemistryX-ray photoelectron spectroscopyChemical engineeringPhysisorptionParticle sizeCatalysis Today
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Insights into localized manipulation of organogel-related microcrystalline spherulite formation

2015

Abstract The formation processes of microcrystalline spherulitic fiber systems related to bile acid amides were determined to include dominant interface-related aspects, the role of which were studied in terms of potential manipulation and increased control over the overall structure of the networks. The nucleation and growth properties and aggregation of two lithocholyl amide derivatives were studied in several organic solvents using thermomicroscopy, as well as thermal control at macroscopic level. Nucleation/crystallization at interfaces was observed to act as the main route for the formation of microcrystalline fibers/solids in six gelator–solvent systems, in which spherulite formation …

Materials scienceSpheruliteOrganogelNucleationFiber networkSpherulite (polymer physics)InterfaceThermal controllaw.inventionCrystallographyColloid and Surface ChemistryMicrocrystallineChemical engineeringlawBile acid amideNucleationFiberCrystallizationCrystallizationta116Topology (chemistry)Colloids and Surfaces A: Physicochemical and Engineering Aspects
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Solvent hydrodynamics speed up crystal nucleation in suspensions of hard spheres

2014

We present a computer simulation study on the crystal nucleation process in suspensions of hard spheres, fully taking into account the solvent hydrodynamics. If the dynamics of collodial crystallization were purely diffusive, the crystal nucleation rate densities would drop as the inverse of the solvent viscosity. However, we observe that the nucleation rate densities do not scale in this way, but are enhanced at high viscosities. This effect might explain the large discrepancy between the nuclation rate densities obtained by simulation and experiment that have reported in the literature so far.

Materials scienceStatistical Mechanics (cond-mat.stat-mech)Nucleation: Physics [G04] [Physical chemical mathematical & earth Sciences]General Physics and AstronomyThermodynamicsFOS: Physical sciencesHard spheresCondensed Matter - Soft Condensed Matterlaw.inventionSolventCrystalViscosity: Physique [G04] [Physique chimie mathématiques & sciences de la terre]lawScientific methodSoft Condensed Matter (cond-mat.soft)CrystallizationCondensed Matter - Statistical Mechanics
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Precursor-mediated crystallization process in suspensions of hard spheres.

2010

We report on a large scale computer simulation study of crystal nucleation in hard spheres. Through a combined analysis of real and reciprocal space data, a picture of a two-step crystallization process is supported: First dense, amorphous clusters form which then act as precursors for the nucleation of well-ordered crystallites. This kind of crystallization process has been previously observed in systems that interact via potentials that have an attractive as well as a repulsive part, most prominently in protein solutions. In this context the effect has been attributed to the presence of metastable fluid-fluid demixing. Our simulations, however, show that a purely repulsive system (that ha…

Materials scienceStatistical Mechanics (cond-mat.stat-mech)NucleationFOS: Physical sciencesGeneral Physics and AstronomyContext (language use)Hard spheresCondensed Matter - Soft Condensed MatterAmorphous solidlaw.inventionCrystalChemical physicslawMetastabilitySoft Condensed Matter (cond-mat.soft)CrystalliteCrystallizationCondensed Matter - Statistical MechanicsPhysical review letters
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Classical nucleation theory for the crystallization kinetics in sheared liquids

2019

While statistical mechanics provides a comprehensive framework for the understanding of equilibrium phase behavior, predicting the kinetics of phase transformations remains a challenge. Classical nucleation theory (CNT) provides a thermodynamic framework to relate the nucleation rate to thermodynamic quantities such as pressure difference and interfacial tension through the nucleation work necessary to spawn critical nuclei. However, it remains unclear whether such an approach can be extended to the crystallization of driven melts that are subjected to mechanical stresses and flows. Here, we demonstrate numerically for hard spheres that the impact of simple shear on the crystallization rate…

Materials scienceStatistical Mechanics (cond-mat.stat-mech)NucleationFOS: Physical sciencesThermodynamicsHard spheresStatistical mechanicsComputational Physics (physics.comp-ph)law.inventionPhysics::Fluid DynamicsShear modulusSurface tensionSimple shearlawClassical nucleation theoryCrystallizationPhysics - Computational PhysicsCondensed Matter - Statistical MechanicsPhysical Review E
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Do the contact angle and line tension of surface-attached droplets depend on the radius of curvature?

2018

Results from Monte Carlo simulations of wall-attached droplets in the three-dimensional Ising lattice gas model and in a symmetric binary Lennard-Jones fluid, confined by antisymmetric walls, are analyzed, with the aim to estimate the dependence of the contact angle $(\Theta)$ on the droplet radius $(R)$ of curvature. Sphere-cap shape of the wall-attached droplets is assumed throughout. An approach, based purely on "thermodynamic" observables, e.g., chemical potential, excess density due to the droplet, etc., is used, to avoid ambiguities in the decision which particles belong (or do not belong, respectively) to the droplet. It is found that the results are compatible with a variation $[\Th…

Materials scienceStatistical Mechanics (cond-mat.stat-mech)Tension (physics)Antisymmetric relationMonte Carlo methodNucleationFOS: Physical sciences02 engineering and technologyMechanicsCondensed Matter - Soft Condensed Matter021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesRadius of curvature (optics)Contact anglePhysics::Fluid Dynamics0103 physical sciencesThermodynamic limitSoft Condensed Matter (cond-mat.soft)General Materials Science010306 general physics0210 nano-technologyCondensed Matter - Statistical MechanicsLine (formation)
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Selective Synthesis of Monodisperse CoO Nanooctahedra as Catalysts for Electrochemical Water Oxidation

2020

Thermal decomposition is a promising route for the synthesis of metal oxide nanoparticles because size and morphology can be tuned by minute control of the reaction variables. We synthesized CoO nanooctahedra with diameters of ∼48 nm and a narrow size distribution. Full control over nanoparticle size and morphology could be obtained by controlling the reaction time, surfactant ratio, and reactant concentrations. We show that the particle size does not increase monotonically with time or surfactant concentration but passes through minima or maxima. We unravel the critical role of the surfactants in nucleation and growth and rationalize the observed experimental trends in accordance with simu…

Materials scienceThermal decompositionDispersityOxygen evolutionNucleationNanoparticle02 engineering and technologySurfaces and Interfaces010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsElectrochemistry01 natural sciences0104 chemical sciencesCatalysisChemical engineeringElectrochemistryGeneral Materials ScienceParticle size0210 nano-technologySpectroscopyLangmuir
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