Search results for "Orthorhombic crystal system"

showing 10 items of 205 documents

High-pressure study of the behavior of mineral barite by x-ray diffraction

2011

In this paper, we report the angle-dispersive x-ray diffraction data of barite, BaSO 4, measured in a diamond-anvil cell up to a pressure of 48 GPa, using three different fluid pressure-transmitting media (methanol-ethanol mixture, silicone oil, and He). Our results show that BaSO 4 exhibits a phase transition at pressures that range from 15 to 27 GPa, depending on the pressure media used. This indicates that nonhydrostatic stresses have a crucial role in the high-pressure behavior of this compound. The new high-pressure (HP) phase has been solved and refined from powder data, having an orthorhombic P2 12 12 1 structure. The pressure dependence of the structural parameters of both room- and…

DiffractionPhase transitionMaterials scienceHigh-pressureAnalytical chemistryDensityHigh pressure (Technology)BaSO4symbols.namesakeBariteCationsPhase (matter)Barium compoundsCompostos de bariRamanMineralTemperatureOxidesTecnologia de les altes pressionsCondensed Matter PhysicsX-ray diffractionElectronic Optical and Magnetic MaterialsFISICA APLICADAHigh pressureTransitionX-ray crystallographysymbolsOrthorhombic crystal systemRaman spectroscopyBASO4Physical Review B
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Structural and vibrational behavior of cubic Cu1.80(3)Se cuprous selenide, berzelianite, under compression

2020

[EN] We have performed an experimental study of the crystal structure and lattice dynamics of cubic Cu1.80(3)Se at ambient temperature and high pressures. Two reversible phase transitions were found at 2.9 and 8.7 GPa. The indexation of the angle-dispersive synchrotron x-ray diffraction patterns suggests a large orthorhombic cell and a monoclinic cell for the high-pressure phases. Raman measurements provide additional information on the local structure. The compressibility of the three ambient temperature phases has been determined and compared to that of other sulphides and selenides.

DiffractionPhase transitionMaterials scienceHigh-pressureBerzelianiteAnalytical chemistry02 engineering and technologyCrystal structure010402 general chemistry01 natural scienceslaw.inventionchemistry.chemical_compoundsymbols.namesakelawSelenideMaterials ChemistryCompressibilityMechanical EngineeringCrystal structureMetals and Alloys021001 nanoscience & nanotechnologySynchrotron0104 chemical scienceschemistryMechanics of MaterialsPhase transitionsFISICA APLICADAsymbolsOrthorhombic crystal system0210 nano-technologyRaman spectroscopyMonoclinic crystal systemCopper selenide
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An electron diffraction study of deposited docosanoic acid monolayers

1991

Docosanoic acid monolayers deposited on thin polymer films under different water surface conditions have been investigated using transmission electron diffraction at normal and tilted incidence. Diffraction patterns obtained from the L2 and L2' phase are quite similar, but distinctly different to samples coated from the CS phase. The former were consistent with molecules perpendicular to the substrate, arranged in a texture of grains with unusual orthorhombic packing. There is evidence for a phase transition from a liquid crystalline phase on the water surface.

DiffractionPhase transitionMaterials sciencePolymers and PlasticsOrganic ChemistrySubstrate (electronics)Condensed Matter PhysicsCrystallographyElectron diffractionPhase (matter)MonolayerMaterials ChemistryOrthorhombic crystal systemTexture (crystalline)Makromolekulare Chemie. Macromolecular Symposia
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Structure and superconducting properties of YBa2(Cu1−x Fex)3O7

1988

Fe-substituted Y-Ba-Cu superconducting oxide compounds were investigated by dc-magnetic susceptibility measurements, powder X-ray diffraction and Mdssbauer spectroscopy. Fe substitution caused a structural transformation from orthorhombic to tetragonal. Up to 4 at% Fe Tc was almost unaffected. It was found that superconductivity in Cu oxides does not depend on orthorhombic crystal symmetry.

DiffractionSuperconductivityMaterials scienceCondensed matter physicsOxideEnergy Engineering and Power TechnologyCondensed Matter PhysicsStructural transformationElectronic Optical and Magnetic MaterialsTetragonal crystal systemCrystallographychemistry.chemical_compoundchemistryOrthorhombic crystal systemElectrical and Electronic EngineeringSpectroscopyPhysica C: Superconductivity
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New polymorph of InVO4: A high-pressure structure with six-coordinated vanadium

2013

A new wolframite-type polymorph of InVO4 is identified under compression near 7 GPa by in situ high-pressure (HP) X-ray diffraction (XRD) and Raman spectroscopic investigations on the stable orthorhombic InVO4. The structural transition is accompanied by a large volume collapse (Delta V/V = -14%) and a drastic increase in bulk modulus (from 69 to 168 GPa). Both techniques also show the existence of a third phase coexisting with the low- and high-pressure phases in a limited pressure range close to the transition pressure. XRD studies revealed a highly anisotropic compression in orthorhombic InVO4. In addition, the compressibility becomes nonlinear in the HP polymorph. The volume collapse in…

DiffractionVanadiumchemistry.chemical_elementOrtho-vanadatesInorganic Chemistrysymbols.namesakeThird phaseVisible-light irradiationFormsPhysical and Theoretical ChemistrySpectroscopySpectroscopyBulk modulusCRYSTALChemistryCRVO4TIVO4CrystallographyPhaseFISICA APLICADATransitionCompressibilitysymbolsOrthorhombic crystal systemRaman spectroscopyDiffraction
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Polymorphism in Strontium Tungstate SrWO 4 under Quasi-Hydrostatic Compression

2016

The structural and vibrational properties of SrWO4 have been studied experimentally up to 27 and 46 GPa, respectively, by angle-dispersive synchrotron X-ray diffraction and Raman spectroscopy measurements as well as using ab initio calculations. The existence of four polymorphs upon quasi-hydrostatic compression is reported. The three phase transitions were found at 11.5, 19.0, and 39.5 GPa. The ambient-pressure SrWO4 tetragonal scheelite-type structure (S.G. I41/a) undergoes a transition to a monoclinic fergusonite-type structure (S.G. I2/a) at 11.5 GPa with a 1.5% volume decrease. Subsequently, at 19.0 GPa, another structural transformation takes place. Our calculations indicate two possi…

Diffraction[PHYS]Physics [physics]02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesInorganic Chemistrychemistry.chemical_compoundsymbols.namesakeCrystallographyTetragonal crystal systemTungstatechemistryPolymorphism (materials science)Ab initio quantum chemistry methods0103 physical sciencessymbolsOrthorhombic crystal systemPhysical and Theoretical Chemistry010306 general physics0210 nano-technologyRaman spectroscopyComputingMilieux_MISCELLANEOUSMonoclinic crystal system
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Electric relaxation and Mn3+/Mn4+ charge transfer in Fe-doped Bi12MnO20–BiMn2O5 structural self-composite

2016

Fe-doped Bi12MnO20–BiMn2O5 ceramics was sintered at 1130 K for 6 h in ambient air. Two centro-symmetric phases formed thermodynamically stable self-composite material that was deduced from X-ray pattern analysis. The lattice parameters were a = 10.147(8) Å—for the cubic I23 Bi12MnO20 phase; and a = 7.545(4) Å, b = 8.538(1) Å, c = 5.758(3) Å—for the orthorhombic Pbam BiMn2O5 phase. The 57Fe Mössbauer spectrum, recorded at room temperature, has shown pure electronic quadrupolar split. The major doublets reflected the occurrence of Fe3+ ions distributed in two sites, i.e., octahedral Fe4+O6 and square pyramidal Fe3+O5, with preferential occupation of the pyramidal sites, that was consistent wi…

Electric relaxationMaterials scienceMechanical EngineeringAnalytical chemistrycharge transfer02 engineering and technologyActivation energy010402 general chemistry021001 nanoscience & nanotechnologyPolaron01 natural sciences7. Clean energySquare pyramidal molecular geometry0104 chemical sciencesIonCrystallographyOctahedronMaterials Science(all)Mechanics of MaterialsLattice (order)Mössbauer spectroscopy:NATURAL SCIENCES:Physics [Research Subject Categories]General Materials ScienceOrthorhombic crystal system0210 nano-technologyJournal of Materials Science
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High-pressure structural and elastic properties of Tl2O3

2014

The structural properties of Thallium (III) oxide (Tl2O3) have been studied both experimentally and theoretically under compression at room temperature. X-ray powder diffraction measurements up to 37.7 GPa have been complemented with ab initio total-energy calculations. The equation of state of Tl2O3 has been determined and compared to related compounds. It has been found experimentally that Tl2O3 remains in its initial cubic bixbyite-type structure up to 22.0 GPa. At this pressure, the onset of amorphization is observed, being the sample fully amorphous at 25.2 GPa. The sample retains the amorphous state after pressure release. To understand the pressure-induced amorphization process, we h…

Equation of statePhase transitionMaterials scienceAb initioOxideGeneral Physics and AstronomyThermodynamicsFOS: Physical sciencesInitio molecular-dynamicsHigh-temperatureInduced amorphizationchemistry.chemical_compoundX-Ray DiffractionTotal-Energy calculationsCondensed Matter - Materials ScienceSingle crystalMaterials Science (cond-mat.mtrl-sci)Compression (physics)Crystal thallic oxideAmorphous solidchemistryAugmented-wave methodFISICA APLICADAElectrical-conductionOrthorhombic crystal systemPhase-transformationPowder diffraction
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Pressure Impact on the Stability and Distortion of the Crystal Structure of CeScO3

2017

[EN] The effects of high pressure on the crystal structure of orthorhombic (Pnma) perovskite-type cerium scandate were studied in situ under high pressure by means of synchrotron X-ray powder diffraction, using a diamond-anvil cell. We found that the perovskite-type crystal structure remains stable up to 40 GPa, the highest pressure reached in the experiments. The evolution of unit-cell parameters with pressure indicated an anisotropic compression. The room-temperature pressure¿volume equation of state (EOS) obtained from the experiments indicated the EOS parameters V0 = 262.5(3) Å3 , B0 = 165(7) GPa, and B0¿ = 6.3(5). From the evolution of microscopic structural parameters like bond distan…

Equation of stateXRDFOS: Physical scienceschemistry.chemical_elementThermodynamics02 engineering and technologyCrystal structurePerovskite01 natural sciencesInorganic ChemistryPhysics - Chemical Physics0103 physical sciencesScandiumPhysical and Theoretical Chemistry010306 general physicsAnisotropyPerovskite (structure)Chemical Physics (physics.chem-ph)Condensed Matter - Materials ScienceCrystal structureMaterials Science (cond-mat.mtrl-sci)021001 nanoscience & nanotechnologyCerium scandateCondensed Matter - Other Condensed MatterHigh pressureCeriumchemistryFISICA APLICADAOrthorhombic crystal system0210 nano-technologyPowder diffractionOther Condensed Matter (cond-mat.other)Inorganic Chemistry
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Spin crossover behavior in a series of iron(III) alkoxide complexes.

2015

The synthesis, crystal structures, magnetic behavior, and electron paramagnetic resonance studies of five new FeIII spin crossover (SCO) complexes are reported. The [FeIIIN5O] coordination core is constituted of the pentadentate ligand bztpen (N5) and a series of alkoxide anions (ethoxide, propoxide, n-butoxide, isobutoxide, and ethylene glycoxide). The methoxide derivative previously reported by us is also reinvestigated. The six complexes crystallize in the orthorhombic Pbca space group and show similar molecular structures and crystal packing. The coordination octahedron is strongly distorted in both the high- and low-temperature structures. The structural changes upon spin conversion ar…

FE(3-OET-SALAPA)2>(CLO4).SInorganic chemistryFERRIC COMPLEXESCrystal structureMethoxideLIGAND; SYSTEMMAGNETIC-SUSCEPTIBILITYlaw.inventionInorganic Chemistrychemistry.chemical_compoundlawSpin crossoverPhysical and Theoretical ChemistryElectron paramagnetic resonanceSchiff baseLigandIRONCrystallographySOLID-STATEchemistryFISICA APLICADAAlkoxideMOSSBAUEROrthorhombic crystal systemPHASE-TRANSITIONSLIGANDSYSTEMSOLVATEInorganic chemistry
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