Search results for "magnetic material"

showing 10 items of 4725 documents

Pullout Force and Inlet Oscillation in Telescopic Carbon Nanotubes: A Quantum Study

2021

The noncovalent interaction energy as a function of the core extension in double-walled carbon nanotubes (DWCNT) was accurately calculated in the frame of density functional theory, considering dis...

geographygeography.geographical_feature_categoryMaterials scienceOscillation02 engineering and technologyInteraction energyCarbon nanotubeMechanics010402 general chemistry021001 nanoscience & nanotechnologyInlet01 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionCore (optical fiber)General EnergylawDensity functional theoryPhysical and Theoretical Chemistry0210 nano-technologyQuantumThe Journal of Physical Chemistry C
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Very strong −N–X+⋯−O–N+ halogen bonds

2016

A new (-)N-X(+)(-)O-N(+) paradigm for halogen bonding is established by using an oxygen atom as an unusual halogen bond acceptor. The strategy yielded extremely strong halogen bonded complexes with very high association constants characterized in either CDCl3 or acetone-d6 solution by (1)H NMR titrations and in the solid-state by single crystal X-ray analysis. The obtained halogen bond interactions, RXB, in the solid-state are found to be in the order of strong hydrogen bonds, viz. RXB ≈ RHB.

halogen bondsNanotechnologychemistry010402 general chemistry01 natural sciencesCatalysisoxygen atomMaterials Chemistryta116Halogen bond010405 organic chemistryChemistryHydrogen bondMetals and AlloysGeneral ChemistryAcceptor0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyOxygen atomHalogenCeramics and CompositesProton NMRTitrationSingle crystalChemical Communications
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Heat capacity and thermal conductivity of multiferroics Bi1-xPrxFeO3

2019

The heat capacity and thermal conductivity of multiferroics Bi1–xPrxFeO3 (0 ≤ x ≤ 0.50) has been studied in the temperature range of 130–800 K. A slight substitution of praseodymium for bismuth is found to lead to a noticeable shift of the antiferromagnetic phase transition temperature whilst the heat capacity increases. The temperature dependences of the heat capacity and thermal conductivity exhibit additional anomalies during phase transitions. The experimental results suggest that the excess heat capacity can be attributed to the Schottky effect for three-level states. The basic mechanisms of the heat transfer of phonons are highlighted and the dependence of the mean free path on temper…

heat capacityMaterials sciencePraseodymiumMultiferroicschemistry.chemical_elementThermodynamics02 engineering and technology01 natural sciencesHeat capacityBismuthThermal conductivity0103 physical sciencesMaterials Chemistry:NATURAL SCIENCES:Physics [Research Subject Categories]Multiferroicsthermal conductivityElectrical and Electronic Engineering010302 applied physicsAtmospheric temperature range021001 nanoscience & nanotechnologyCondensed Matter PhysicsElectronic Optical and Magnetic MaterialschemistryControl and Systems EngineeringCeramics and Composites0210 nano-technology
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A Computational Study of Adsorption of CO2, SO2, and H2CO on Free-Standing and Molybdenum-Supported CaO Films

2018

Oxide films play a significant role in a wide range of fields from catalysis to solar cell materials. CaO films are promising sorbents for many environmentally harmful molecules. Here, we report a systematic investigation of adsorption of CO2, SO2, and H2CO on bulk and Mo-supported CaO(100) films using density functional theory. Significant effects on adsorption energy, charge transfer to the molecules, and degree of the C–O bond activation were demonstrated on Mo-supported CaO films by changing the film thickness, composition, and the strength and direction of an applied external electric field. These findings are relevant for interpreting results from scanning tunneling microscopy of smal…

hiilidioksidiMaterials scienceOxidechemistry.chemical_element02 engineering and technology010402 general chemistry01 natural scienceslaw.inventionCatalysisMetalchemistry.chemical_compoundAdsorptionlawMoleculePhysical and Theoretical Chemistryta116ta114carbon dioxide021001 nanoscience & nanotechnologylaskennallinen kemiacomputational chemistry0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyChemical engineeringchemistryrikkidioksidithin filmsMolybdenumadsorptionvisual_artvisual_art.visual_art_mediumsulphur dioxideformaldehydeDensity functional theoryScanning tunneling microscopeohutkalvot0210 nano-technologyadsorptioformaldehydiJournal of Physical Chemistry C
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Design and performance of the prototype Schwarzschild-Couder telescope camera

2022

Journal of astronomical telescopes, instruments, and systems 8(01), 014007-1 (2022). doi:10.1117/1.JATIS.8.1.014007

imaging atmospheric Cherenkov telescopesinstrumentationPhysics - Instrumentation and Detectorsvery-high-energy gamma-ray astronomyPhysics::Instrumentation and DetectorsMechanical EngineeringSettore FIS/01 - Fisica SperimentaleAstrophysics::Instrumentation and Methods for AstrophysicsFOS: Physical sciencesAstronomy and AstrophysicsInstrumentation and Detectors (physics.ins-det)530Electronic Optical and Magnetic MaterialsCherenkov telescope arraySpace and Planetary ScienceControl and Systems Engineeringddc:530prototype Schwarzschild-Couder telescopeAstrophysics - Instrumentation and Methods for AstrophysicsInstrumentation and Methods for Astrophysics (astro-ph.IM)silicon photomultipliers
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Asymmetric [N–I–N]+halonium complexes in solution?

2020

Assessment of the solution equilibria of [bis(pyridine)iodine(I)]+ complexes by ESI-MS and NMR reveals the preference of iodine(I) to form complexes with a more basic pyridine. Mixtures of symmetric [bis(pyridine)iodine(I)]+ complexes undergo statistical ligand exchange, with a predominant entropic driving force favoring asymmetric systems. The influence of ligand basicity, concentration, temperature, and ligand composition is evaluated. Our findings are expected to facilitate the investigations, and the supramolecular and synthetic applications of halonium ions’ halogen bonds. peerReviewed

inorganic chemicals2019-20 coronavirus outbreakliuoksetLigandMetals and AlloysSupramolecular chemistrychemistry.chemical_elementliganditkompleksiyhdisteetGeneral ChemistryIodineMedicinal chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonjodichemistry.chemical_compoundchemistryPyridineHalogenMaterials ChemistryCeramics and CompositesHalonium ionChemical Communications
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Potent affinity material for tracing acetone and related analytes based on molecular recognition by halogen bonds.

2014

Affinity materials based on halogen bonds turned out to be a powerful tool for the molecular recognition of acetone or related carbonyl compounds in the presence of ubiquitous protic molecules. The superior selectivity and sensitivity were found by the gravimetric detection of volatile organic compounds by quartz crystal microbalances.

inorganic chemicalsAnalyteMetals and AlloysGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystalchemistry.chemical_compoundMolecular recognitionchemistryHalogenMaterials ChemistryCeramics and CompositesAcetoneMoleculeOrganic chemistryGravimetric analysisSelectivityChemical communications (Cambridge, England)
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Structural Changes of Titanium Oxide Induced by Chromium Addition as Determined by an X-Ray Diffraction Study

1995

Abstract An X-ray diffraction study has been carried out on a series of polycrystalline TiO 2 (anatase) catalysts containing Cr(III) at different atomic concentrations (0.2-5.0 at. %), prepared by a co-precipitation method. Analysis of the variation of the unit cell parameters of chromium-doped anatase with respect to pure anatase has allowed us to estimate the solubility limit for the system at around 1.4 at. %. There is no evidence for the existence of a separate crystalline chromium oxide phase. Temperature effects on the cell parameter and on the anatase-rutile transformation rate were also analyzed. An increase in temperature produced release of the chromium from the solid solution. At…

inorganic chemicalsAnataseMaterials scienceInorganic chemistrytechnology industry and agricultureAnalytical chemistrychemistry.chemical_elementCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsTitanium oxideInorganic ChemistryChromiumchemistryPhase (matter)X-ray crystallographyMaterials ChemistryCeramics and CompositesCrystallitePhysical and Theoretical ChemistrySolubilitySolid solutionJournal of Solid State Chemistry
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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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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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