Search results for "Fine structure"

showing 10 items of 656 documents

Geometric, electronic, and magnetic structure ofCo2FeSi: Curie temperature and magnetic moment measurements and calculations

2005

In this work a simple concept was used for a systematic search for materials with high spin polarization. It is based on two semiempirical models. First, the Slater-Pauling rule was used for estimation of the magnetic moment. This model is well supported by electronic structure calculations. The second model was found particularly for ${\mathrm{Co}}_{2}$ based Heusler compounds when comparing their magnetic properties. It turned out that these compounds exhibit seemingly a linear dependence of the Curie temperature as function of the magnetic moment. Stimulated by these models, ${\mathrm{Co}}_{2}\mathrm{FeSi}$ was revisited. The compound was investigated in detail concerning its geometrical…

Curie–Weiss lawMaterials scienceExtended X-ray absorption fine structureCondensed matter physicsMagnetic momentMagnetic structureCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsCondensed Matter::Materials ScienceMagnetizationParamagnetismCurie's lawCurie temperatureCondensed Matter::Strongly Correlated ElectronsPhysical Review B
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Spin-Crossover and Liquid Crystal Properties in 2D Cyanide-Bridged FeII−MI/II Metalorganic Frameworks

2010

Novel two-dimensional heterometallic Fe(II)-M(Ni(II), Pd(II), Pt(II), Ag(I), and Au(I)) cyanide-bridged metalorganic frameworks exhibiting spin-crossover and liquid crystal properties, formulated as {FeL(2)[M(I/II)(CN)(x)](y)}·sH(2)O, where L are the ligands 4-(4-alkoxyphenyl)pyridine, 4-(3,4-dialkoxyphenyl)pyridine, and 4-(3,4,5-trisalkoxyphenyl)pyridine, have been synthesized and characterized. The physical characterization has been carried out by means of EXAFS, X-ray powder diffraction, magnetic susceptibility, differential scanning measurements, and Mössbauer spectroscopy. The 2D Fe(II) metallomesogens undergo incomplete and continuous thermally induced spin transition at T(1/2) ≈ 170 …

CyanidesMolecular StructureExtended X-ray absorption fine structure010405 organic chemistrySpin transitionStereoisomerismLigands010402 general chemistry01 natural sciencesMagnetic susceptibilityLiquid Crystals0104 chemical sciences3. Good healthInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryLiquid crystalSpin crossoverMetals HeavyMössbauer spectroscopyPyridineOrganometallic CompoundsPhysical and Theoretical ChemistryPowder diffractionInorganic Chemistry
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Long-Range and Short-Range Structure of Proton-Conducting Y:BaZrO3

2011

Yttrium-doped barium zirconate (BZY) is the most promising candidate for proton-conducting ceramics and has been extensively studied in recent years. The detailed features of the crystal structure, both short-range and long-range, as well as the crystal chemistry driving the doping process, are largely unknown. We use very high resolution X-ray diffraction (HR-XRD) to resolve the crystal structure, which is very slightly tetragonally distorted in BZY, while the local environment around Zr4+ and Y3+ is probed with extended X-ray absorption fine structure (EXAFS), and the symmetry and vibrations are investigated by using Raman spectroscopy. It is found that barium zirconate shows some degree …

DYNAMICSRAMAN-SCATTERINGMaterials scienceCrystal chemistryGeneral Chemical EngineeringYTTRIUMRAMAN-SCATTERING; LOCAL ENVIRONMENT; BARIUM CERATE; SPECTROSCOPY; YTTRIUM; BAZR0.9Y0.1O2.95; STRONTIUM; DYNAMICS; DEFECTS; OXIDESCrystal structuresymbols.namesakeSTRONTIUMMaterials ChemistryLOCAL ENVIRONMENTBAZR0.9Y0.1O2.95OXIDESSpectroscopyProton conductorSPECTROSCOPYExtended X-ray absorption fine structureDopingDEFECTSGeneral ChemistryCrystallographysymbolsRaman spectroscopyBARIUM CERATERaman scatteringChemistry of Materials
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Adsorption mechanism of arsenate by zirconyl-functionalized activated carbon

2007

Arsenate [As(V)] and arsenite [As(III)] sorption at the solid-water interface of activated carbon impregnated with zirconyl nitrate (Zr-AC) was investigated using X-ray absorption spectroscopy (XAS) and surface complexation modeling. The XAS data at the Zr K-edge suggest that the structure of the zirconyl nitrate coating is built from chains of edge-sharing ZrO8 trigonal dodecahedra bound to each other through two double hydroxyl bridges. The 8-fold coordination of each Zr atom is completed by four O atoms, which share a bit less than the two theoretically possible bidentate nitrate groups. On impregnation, two of the O atoms may lose their nitrate group and be transformed to hydroxyl group…

DenticityArsenitesSurface PropertiesInorganic chemistrychemistry.chemical_elementchemistry [Arsenites]Biomaterialschemistry.chemical_compoundColloid and Surface ChemistryAdsorptionOxidation statechemistry [Arsenates]medicineArsenicchemistry [Zirconium]ArseniteNitrateschemistry [Nitrates]Extended X-ray absorption fine structureSpectrum AnalysisX-Rayschemistry [Water]arsenic acidArsenateWaterCarbonchemistry [Carbon]Surfaces Coatings and FilmsElectronic Optical and Magnetic Materialsarsenitechemistryddc:540PotentiometryArsenatesAdsorptionZirconiumActivated carbonmedicine.drugJournal of Colloid and Interface Science
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Resonance ionization mass spectroscopy for trace analysis of neptunium

1993

Resonance ionization mass spectroscopic (RIMS) measurements for trace analysis and spectroscopy of 237Np, the ecologically most important isotope of neptunium, are described. The chemical procedure for the separation of neptunium from aqueous samples as well as the preparation of filaments for RIMS are outlined. Several two- and three-step excitation schemes have been investigated in order to find suitable conditions for the sensitive detection of 237Np. Using a three-step, three-color excitation and ionization scheme an overall detection efficiency of 3×10−8 was obtained, resulting in a detection limit of 4×108 atoms (160 fg) of 237Np. The hyperfine structure splittings of the levels under…

Detection limitMaterials sciencePhysics and Astronomy (miscellaneous)NeptuniumGeneral EngineeringAnalytical chemistryGeneral Physics and Astronomychemistry.chemical_elementPhotoionizationMass spectrometryNuclear magnetic resonancechemistryIonizationIonization energySpectroscopyHyperfine structureApplied Physics B Photophysics and Laser Chemistry
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Pulsed EPR determination of water accessibility to spin-labeled amino acid residues in LHCIIb.

2009

Membrane proteins reside in a structured environment in which some of their residues are accessible to water, some are in contact with alkyl chains of lipid molecules, and some are buried in the protein. Water accessibility of residues may change during folding or function-related structural dynamics. Several techniques based on the combination of pulsed electron paramagnetic resonance (EPR) with site-directed spin labeling can be used to quantify such water accessibility. Accessibility parameters for different residues in major plant light-harvesting complex IIb are determined by electron spin echo envelope modulation spectroscopy in the presence of deuterated water, deuterium contrast in …

DetergentsBiophysicsLight-Harvesting Protein ComplexesSpectroscopy Imaging and Other TechniquesBuffersCrystallography X-RaySpectral linelaw.inventionlawMoleculeHumansAmino AcidsElectron paramagnetic resonanceProtein Structure QuaternaryHyperfine structureAlkylPlant Proteinschemistry.chemical_classificationPulsed EPRChemistryElectron Spin Resonance SpectroscopyPeasTemperatureWaterSite-directed spin labelingCrystallographyDeuteriumSolubilityMutationSolventsSpin LabelsProtein MultimerizationBiophysical journal
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Effect of pressure on the structural properties and electronic band structure of GaSe

2007

The structural properties of GaSe have been investigated up to 38 GPa by monochromatic X-ray diffraction. The onset of the phase transition from the e-GaSe to a disordered NaCi-type structural motif is observed near 21 GPa. Using the experimentally determined lattice parameters of the layered e-phase as input, constrained ab-initio total energy calculations were performed in order to optimize the internal structural parameters at different pressures. The results obtained for the nearest-neighbor Ga-Se distance agree with those derived from recent EXAFS measurements. In addition, information is obtained on the changes of Ga-Ga and Se-Se bond lengths which were not accessible to a direct expe…

DiffractionBond lengthCrystallographyPhase transitionExtended X-ray absorption fine structureBand gapChemistryAb initio quantum chemistry methodsElectronic structureCondensed Matter PhysicsElectronic band structureMolecular physicsElectronic Optical and Magnetic Materialsphysica status solidi (b)
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<title>In-situ x-ray absorption fine structure and x-ray diffraction studies of hydrogen intercalation in tungsten oxides</title>

1997

We present in-situ x-ray absorption fine structure (XAFS) (at the W L 3 -edge) and x-ray diffraction (XRD) studies of hydrogen intercalation into stable monoclinic (m-WO 3 ) and metastable hexagonal (h-WO 3 ) and cubic (c-WO 3 ) phases of tungsten oxide. The analysis of XAFS and XRD data allowed us to reconstruct the local environment around tungsten ions in the first coordination shell. The obtained results are compared with the existing structural models.

DiffractionCrystallographyMaterials scienceHydrogenchemistryIntercalation (chemistry)X-ray crystallographychemistry.chemical_elementTungstenAbsorption (chemistry)X-ray absorption fine structureMonoclinic crystal systemSPIE Proceedings
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Atomistic simulations of the FeK-edge EXAFS in FeF3using molecular dynamics and reverse Monte Carlo methods

2016

Atomistic simulations of the experimental Fe K-edge extended x-ray absorption fine structure (EXAFS) of rhombohedral (space group ) FeF3 at T = 300 K were performed using classical molecular dynamics and reverse Monte Carlo (RMC) methods. The use of two complementary theoretical approaches allowed us to account accurately for thermal disorder effects in EXAFS and to validate the developed force-field model, which was constructed as a sum of two-body Buckingham-type (Fe–F and F–F), three-body harmonic (Fe–F–Fe) and Coulomb potentials. We found that the shape of the Fe K-edge EXAFS spectrum of FeF3 is a more sensitive probe for the determination of potential parameters than the values of stru…

DiffractionMaterials scienceExtended X-ray absorption fine structureAb initio02 engineering and technologyReverse Monte Carlo010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesAtomic and Molecular Physics and OpticsSpectral lineEffective nuclear charge0104 chemical sciencesCondensed Matter::Materials ScienceMolecular dynamicsK-edgeAtomic physics0210 nano-technologyMathematical PhysicsPhysica Scripta
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Crossing the boundary between face-centred cubic and hexagonal close packed: the structure of nanosized cobalt is unraveled by a model accounting for…

2014

The properties of nanostructured cobalt in the fields of magnetic, catalytic and biomaterials depend critically on Co close packing. This paper reports a structural analysis of nanosized cobalt based on the whole X-ray diffraction (XRD) pattern simulation allowed by the Debye equation. The underlying structural model involves statistical sequences of cobalt layers and produces simulated XRD powder patterns bearing the concurrent signatures of hexagonal and cubic close packing (h.c.p. and f.c.c.). Shape, size distribution and distance distribution between pairs of atoms are also modelled. The simulation algorithm allows straightforward fitting to experimental data and hence the quantitative …

DiffractionMaterials scienceExtended X-ray absorption fine structureClose-packing of equal spheresStackingAb initiochemistry.chemical_elementMolecular physicsGeneral Biochemistry Genetics and Molecular BiologyXANESCondensed Matter::Materials ScienceCrystallographysymbols.namesakechemistryDebye–Hückel equationsymbolsCobaltJournal of Applied Crystallography
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