Search results for "Powder diffraction"

showing 10 items of 243 documents

Crystal structure analysis of a star-shaped triazine compound: a combination of single-crystal three-dimensional electron diffraction and powder X-ra…

2017

The solid-state structure of star-shaped 2,4,6-tris{(E)-2-[4-(dimethylamino)-phenyl]ethenyl}-1,3,5-triazine is determined from a powder sample by exploiting the respective strengths of single-crystal three-dimensional electron diffraction and powder X-ray diffraction data. The unit-cell parameters were determined from single crystal electron diffraction data. Using this information, the powder X-ray diffraction data were indexed, and the crystal structure was determined from the powder diffraction profile. The compound crystallizes in a noncentrosymmetric space group,P212121. The molecular conformation in the crystal structure was used to calculate the molecular dipole moment of 3.22 Debye,…

DiffractionChemistryMetals and Alloys02 engineering and technologyCrystal structure010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsDipolesymbols.namesakeCrystallographyElectron diffractionX-ray crystallographyMaterials Chemistrysymbols0210 nano-technologySingle crystalPowder diffractionDebyeActa crystallographica Section B, Structural science, crystal engineering and materials
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High-pressure phase transitions and compressibility of wolframite-type tungstates

2010

This paper reports an investigation on the phase diagram and compressibility of wolframite-type tungstates by means of x-ray powder diffraction and absorption in a diamond-anvil cell and ab initio calculations. The diffraction experiments show that monoclinic wolframite-type MgWO4 suffers at least two phase transitions, the first one being to a triclinic polymorph with a structure similar to that of CuWO4 and FeMoO4-II. The onset of each transition is detected at 17.1 and 31 GPa. In ZnWO4 the onset of the monoclinic-triclinic transition has been also found at 15.1 GPa. These findings are supported by density-functional theory calculations, which predict the occurrence of additional transiti…

DiffractionCondensed Matter - Materials SciencePhase transitionMaterials scienceGeneral Physics and AstronomyThermodynamicsMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesTriclinic crystal systemCondensed Matter - Other Condensed MatterAb initio quantum chemistry methodsPhase (matter)CompressibilityPowder diffractionPhase diagramOther Condensed Matter (cond-mat.other)
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H-bonding schemes of di- and tri-p-benzamides assessed by a combination of electron diffraction, X-ray powder diffraction and solid-state NMR

2010

The crystal structures of di- and tri-p-benzamides are solved by a combination of single crystal, electron and powder X-ray diffraction. Different hydrogen-bonding schemes observed in the two structures are described and classified. The hydrogen-bonding networks are correlated to complementary data obtained from multinuclear solid-state NMR.

DiffractionCrystallographyElectron diffractionChemistryGeneral Materials ScienceGeneral ChemistryNuclear magnetic resonance crystallographyCrystal structureSelected area diffractionCondensed Matter PhysicsSingle crystalPowder diffractionElectron backscatter diffractionCrystEngComm
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Mechanism of pulsed electron irradiation of the PLZT X/65/35 ceramics

2005

The comprehensive study of high-current pulsed electron irradiation effect on the structure and lattice dynamics as well as Atomic Force (AFM) and Laser Confocal Scanning microscope (LSCM) surface imaginaries of PLZT 8/65/35 ceramics have been performed. X-ray powder diffraction studies show the transformation of the cubic perovskite Pm-3m (Z = 1) into orthorhombic Pmmm (Z = 1) structure for the sample irradiated by one pulse (dose 6 × 1014 electrons/cm2) and into cubic Pm-3m with increased lattice volume and more ordered structure at irradiating by 10 and 100 pulses (dose 6 × 1015 and 6 × 1016 el/cm2). A consequence, the changes of number, intensity and phonon modes position occur in Raman…

DiffractionCrystallographysymbols.namesakeMaterials scienceScanning electron microscopeAnalytical chemistrysymbolsElectron beam processingOrthorhombic crystal systemIrradiationElectronRaman spectroscopyPowder diffractionphysica status solidi (c)
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Ferroelectric Domain Walls in BaTiO3: Fingerprints in XRPD Diagrams and Quantitative HRTEM Image Analysis

1997

The structure of ferroelectric domain walls in BaTiO3 has been investigated through two complementary approaches, a global one by the fine analysis of X-ray diffraction patterns, the other essentially local via a quantitative image analysis method developed and applied to High Resolution Transmission Electron Microscopy images. These two original approaches converge towards a clear description of 90○ walls which are shown to be a 4–6 nm wide region where the crystallographic discontinuity is accommodated by irregular atomic displacements. The results given here demonstrate that the usual structural theoretical description of walls commonly accepted for energy calculations are far too simpli…

DiffractionMaterials scienceGeneral EngineeringGeneral Physics and AstronomyMineralogy02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesFerroelectricityComputational physicsDiscontinuity (geotechnical engineering)[PHYS.HIST]Physics [physics]/Physics archives0103 physical sciences010306 general physics0210 nano-technologyHigh-resolution transmission electron microscopyPowder diffractionAnalysis methodJournal de Physique III
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128-Channel Silicon Strip Detector Installed at a Powder Diffractometer

2004

Silicon strip detectors represent a new class of one-dimensional position-sensitive single photon counting devices. They allow a reduction of measurement time at the powder diffractometers by a factor up to 100 compared to instruments with a single counter, while maintaining comparable count statistics. Present work describes a 128-channel detector working with a standard diffractometer. The detector is 12.8 mm long and covers the angular range of 3.2 deg. We discuss the diffraction geometry in real and reciprocal space, the FWHM of diffraction peaks, and the background level. Measurements were made on standard samples and on complex samples of industrial importance (e. g., portland clinker…

DiffractionMaterials scienceSiliconbusiness.industryMechanical EngineeringDetectorchemistry.chemical_elementCondensed Matter PhysicsPhoton countingReciprocal latticeOpticschemistryMechanics of MaterialsPowder DiffractometerGeneral Materials SciencebusinessPowder diffractionDiffractometerMaterials Science Forum
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LiCrO2 Under Pressure: In-Situ Structural and Vibrational Studies

2018

The high-pressure behaviour of LiCrO2, a compound isostructural to the battery compound LiCoO2, has been investigated by synchrotron-based angle-dispersive X-ray powder diffraction, Raman spectroscopy, and resistance measurements up to 41, 30, and 10 Gpa, respectively. The stability of the layered structured compound on a triangular lattice with R-3m space group is confirmed in all three measurements up to the highest pressure reached. The dependence of lattice parameters and unit-cell volume with pressure has been determined from the structural refinements of X-ray diffraction patterns that are used to extract the axial compressibilities and bulk modulus by means of Birch&ndash

DiffractionMaterials sciencehigh-pressureHigh-pressureGeneral Chemical EngineeringThermodynamics02 engineering and technology01 natural sciencesInorganic Chemistrysymbols.namesakeElectrical resistance and conductanceElectrical resistivity and conductivity0103 physical scienceslcsh:QD901-999General Materials ScienceHexagonal lattice010306 general physicsequation of stateBulk modulusEquation of state021001 nanoscience & nanotechnologyCondensed Matter PhysicsX-ray diffractionX-ray crystallographyhigh-pressure; X-ray diffraction; Raman spectroscopy; equation of stateRaman spectroscopysymbolslcsh:Crystallography0210 nano-technologyRaman spectroscopyPowder diffraction
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Electron diffraction, X-ray powder diffraction and pair-distribution-function analyses to determine the crystal structures of Pigment Yellow 213, C23…

2009

The crystal structure of the nanocrystalline alpha phase of Pigment Yellow 213 (P.Y. 213) was solved by a combination of single-crystal electron diffraction and X-ray powder diffraction, despite the poor crystallinity of the material. The molecules form an efficient dense packing, which explains the observed insolubility and weather fastness of the pigment. The pair-distribution function (PDF) of the alpha phase is consistent with the determined crystal structure. The beta phase of P.Y. 213 shows even lower crystal quality, so extracting any structural information directly from the diffraction data is not possible. PDF analysis indicates the beta phase to have a columnar structure with a si…

DiffractionModels MolecularAza CompoundsReflection high-energy electron diffractionChemistryMolecular ConformationGeneral MedicineCrystal structurePair-distribution functionHeterocyclic Compounds 4 or More RingsGeneral Biochemistry Genetics and Molecular BiologyPigment Yellow 213CrystalCrystallinityCrystallographyElectron diffractionElectron diffractionMicroscopy Electron TransmissionX-ray powder diffractionElectron diffraction; Pair-distribution function; Pigment Yellow 213; X-ray powder diffractionParticle SizeColoring AgentsPowder diffractionPowder DiffractionElectron backscatter diffractionActa crystallographica. Section B, Structural science
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Time-resolved X-ray powder diffraction on a three-way catalyst at the GILDA beamline

2003

Time-resolved X-ray diffraction experiments carried out at the beamline BM08-GILDA of ESRF allowed a study of the structural modifications taking place in a Pt/ceria-zirconia catalyst while the CO oxidation reaction was in progress. The capillary tube in which the sample is stored acts effectively as a chemical microreactor that ensures homogeneity of the sample treatments and minimization of diffusion effects. During the flowing of the reactant CO/He mixture, the investigated catalyst undergoes a fast Ce(IV)-Ce(III) partial reduction that involves the release of one O atom for every two reduced Ce cations. Because Ce(III) has a larger ionic radius than Ce(IV), the structural modification p…

DiffractionNuclear and High Energy PhysicsRadiationMaterials scienceIonic radiusAnalytical chemistryCatalysisCrystallographyLattice constantMixed oxideMicroreactorInstrumentationQuadrupole mass analyzerPowder diffraction
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Pressure-induced phase transformations in mineral chalcocite, Cu2S, under hydrostatic conditions

2014

Abstract High-pressure room-temperature angle-dispersive powder X-ray diffraction measurements on Cu2S chalcocite were performed up to 30 GPa using a diamond-anvil cell, He as pressure transmitting medium and synchrotron radiation. Two first-order phase transitions were found at 3.2 and 7.4 GPa. The indexation of the powder diffraction patterns suggests three different monoclinic cells for the low-pressure chalcocite and the two high-pressure phases. Subtle changes in the X-ray diffraction patterns suggest a third pressure-induced transition above 26 GPa. Structural parameters and compressibility are discussed and compared to those reported in a previous study on Cu2S nanowires.

DiffractionPhase transitionChalcociteChemistryMechanical EngineeringMetals and AlloysAnalytical chemistryMineralogySynchrotron radiationmacromolecular substancesengineering.materialPolymorphism (materials science)Mechanics of MaterialsMaterials ChemistryCompressibilityengineeringPowder diffractionMonoclinic crystal systemJournal of Alloys and Compounds
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