Search results for "Solid solution"

showing 10 items of 308 documents

Phase competition in (La1 − c,Src)CoO3solid solutions:ab initiothermodynamic study

2013

Statistical thermodynamics and density functional theory (DFT) formalisms are combined to analyze the phase competition of energetically preferable phases in (La1 − c,Src)CoO3 solid solutions upon LaCoO3 doping with Sr. La/Sr sublattice in ABO3 perovskite structure is considered as immersed in the field of CoO3 units and the superstructures that are stable with respect to the formation of antiphase domains are analyzed. The concentration-dependent energy parameters determining the relative stability of the cubic superstructures (phases) are extracted. This allows us calculations of concentration- and temperature dependences of the long-range order (LRO) parameters for different phases. The …

CrystallographyField (physics)ChemistryPhase (matter)DopingThermodynamicsDensity functional theoryCondensed Matter PhysicsRelative stabilityElectronic Optical and Magnetic MaterialsSolid solutionphysica status solidi (b)
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Structural effects of Co and Cr substitution in LaMnO3 + δ

2000

Series of perovskite oxides with the composition LaMn1 − xMxO3 + δ (M = Cr, Co; 0 ≤ x ≤ 1) have been synthesized by thermal treatment of precursors obtained by freeze-drying of acetic acid solutions. The oxides have been characterized by X-ray diffraction, and the Mn4+ content and, thus, the oxygen excess, δ, has been determined by redox back-titration. LaMnO3.14 and LaCrO3 phases have the rhombohedral-LaAlO3 and the orthorhombic-GdFeO3 structures, respectively. The LaMn1 − xCrxO3 + δ phases have the rhombohedral structure for x ≤ 0.3, and the orthorhombic structure for x ≥ 0.5. LaCoO3 has, as LaMnO3.14, the rhombohedral structure. However, the LaMn1 − xCoxO3 + δ phases have orthorhombic st…

CrystallographyIonic radiusChemistryInorganic chemistryMaterials ChemistryOrthorhombic crystal systemGeneral ChemistryCrystal structureThermal treatmentChemical compositionRedoxPerovskite (structure)Solid solutionJournal of Materials Chemistry
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Influence of diamagnetic impurity on mid‐IR absorption in antiferromagnetic insulator NiO

2005

-1 was studied in polycrystalline Ni c Mg 1-c O solid solutions with c=0.99, 0.98, 0.97, 0.95, 0.90, 0.80, 0.70 and 0.60. The composition and temperature dependences of the absorption suggest that the band has magnetic origin re- lated to simultaneous excitation of two-magnons at the Brillouin-zone boundary and one phonon. -1 in polycrystalline NicMg1-cO solid solutions. Polycrystalline solid solutions NicMg1-cO (c=0.99, 0.98, 0.97, 0.95, 0.90, 0.80, 0.70 and 0.60) were prepared using ceramic technology from the appropriate amounts of aqueous solutions of Mg(NO3)2·6H2O and Ni(NO3)2·6H2O salts, which were mixed and slowly evaporated. The remaining dry 'flakes' were heated up to 500-600 oC to…

CrystallographyMaterials scienceImpurityvisual_artThermal decompositionNon-blocking I/Ovisual_art.visual_art_mediumAnalytical chemistryDiamagnetismAntiferromagnetismCrystalliteCeramicSolid solutionphysica status solidi (c)
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Magnetic Transitions in the Double Perovskite Sr2FeRe1-xFexO6(0≤X≤0.5)

2008

AbstractThe synthesis, structure, and magnetic and transport properties of solid solutions Sr2FeRe1-xFexO6 (0≤x≤0.5) are reported. A structural evolution in the solid solutions from a double perovskite to perovskite is observed with increasing Fe/Re disorder. Except for the metallic parent compound all members of the series are semiconducting. For the Fe-doped samples a change from ferrimagnetic interactions in the parent compound to a complex superposition of ferrimagnetic and antiferromagnetic interactions was observed. The magnetic moment decreases with x, whereas the Curie temperature TC remains unaffected. The magnetic and Mössbauer data suggest Fe to act as a redox-buffer.

CrystallographyMaterials scienceMagnetic momentFerromagnetismFerrimagnetismMössbauer spectroscopyCurie temperatureAntiferromagnetismPerovskite (structure)Solid solutionMRS Proceedings
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<title>Origin of visible photoluminescence in NiO and Ni<formula><inf><roman>c</roman></inf></formula>Mg&lt…

2003

A study of the visible photoluminescence in single-crystal NiO and NicMg1-cO (c = 0.99, 0.98 and 0.95) solid solutions is presented for the first time. Two wide luminescence bands, peaked at approximately 12000 cm-1 and approximately 18500 cm-1, were observed. The dependence of their intensity and position on the excitation energy, temperature, and composition were investigated. We attribute the origin of two photoluminescence bands to the impurity- or defect perturbed Ni2+ excitons.© (2003) COPYRIGHT SPIE--The International Society for Optical Engineering. Downloading of the abstract is permitted for personal use only.

CrystallographyPhotoluminescenceMaterials scienceImpurityExcitonNon-blocking I/OPhotoluminescence excitationLuminescenceSolid solutionIonSPIE Proceedings
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X-ray powder diffraction study of the stability of solid solutions in (La1−xGdx)OCl

1996

The formation of the solid solutions in the (La1−xGdx)OCl series was studied by X-ray powder diffraction (XPD) at room temperature in the 2θ region between 6.5 and 120°. The Rietveld profile refinement analyses of the XPD patterns were carried out with the background, unit cell, atomic position, isotropic temperature, and Gaussian profile form parameters refined freely. All (La1−xGdx)OCl samples possessed the tetragonal PbFCl-type structure with P4/nmm as the space group (Z=2). The unit cell parameters a and c evolve smoothly through the series and no clustering of the Gd3+ ions was observed according to Vegard's law. The solid solubility exists throughout the whole series. The valence bond…

CrystallographyRadiationMaterials scienceX-rayGeneral Materials ScienceCondensed Matter PhysicsInstrumentationPowder diffractionSolid solutionPowder Diffraction
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<title>Primary radiation defect formation in silver halides</title>

1998

Under irradiation the formation of primary intrinsic defects in silver halide solid solutions AgBr1-xClx take place via strong exciton-phonon interaction. Efficiency of these defects formation depend on solid solution composition and within 0 <EQ x <EQ 0.15 dependence on temperature was observed too. Estimation shows efficiency of defects creation is approximately 0.01 for AgCl and noticeably higher for AgBr.© (1998) COPYRIGHT SPIE--The International Society for Optical Engineering. Downloading of the abstract is permitted for personal use only.

Crystallographychemistry.chemical_compoundMaterials scienceSilver halidechemistryPhononExcitonHalidePhysical chemistryIrradiationAbsorption (chemistry)LuminescenceSolid solutionOptical Information Science and Technology (OIST97): Optical Recording Mechanisms and Media
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Crystallization of chiral molecular compounds: what can be learned from the Cambridge Structural Database?

2020

A detailed study on chiral compound structures found in the Cambridge Structural Database (CSD) is presented. Solvates, salts and co-crystals have intentionally been excluded, in order to focus on the most basic structures of single enantiomers, scalemates and racemates. Similarity between the latter and structures of achiral monomolecular compounds has been established and utilized to arrive at important conclusions about crystallization of chiral compounds. For example, the fundamental phenomenon of conglomerate formation and, in particular, their frequency of occurrence is addressed. In addition, rarely occurring kryptoracemates and scalemic compounds (anomalous racemates) are discussed.…

DatabaseFrequency of occurrenceChemistryMetals and AlloysCrystal structurecomputer.software_genreAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic Materialslaw.inventionlawMaterials ChemistryCrystallizationEnantiomercomputerSolid solutionActa Crystallographica Section B Structural Science, Crystal Engineering and Materials
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Synthesis and structural study of NaTi2(PO4)3-NaSn2(PO4)3 solid solutions. I. The effect of composition on lattice parameters

1992

Abstract Compounds NaM2IV(PO4)3 with NZP-type structure present a different behavior depending on the nature of MIV. For MIV = Ti and Zr the structure shows the space group R3c, whereas for MIV = Sn the space group is R3. Differences in behavior of NaTi2(PO4)3 - NaSn2(PO4)3 solid solutions are discussed in relation to the composition. The variation of the lattice parameters with composition in NaTi2−xSnx(PO4)3 (0 1. The structure of the compound with x = 1 (NaSnTi(PO4)3) has been determined applying the Rietveld method to deconvolute the powder x-ray diffraction profile.

DiffractionCrystallographyMechanics of MaterialsChemistryMechanical EngineeringLattice (order)General Materials ScienceCondensed Matter PhysicsSolid solutionMaterials Research Bulletin
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The Effects of Thermo-Baric Synthesis on the Structure and Properties of the Ferroelectric Li0.125Na0.875NbO3Solid Solution

2014

ABSTRACTResults of X-ray diffraction, dielectric, and Raman studies of the ferroelectric Li0.125Na0.875NbO3 solid solution obtained under hot-pressing conditions (6 GPa, 1400 and 1800 K) are compared with those of the same compound synthesized by conventional ceramics technology. The thermo-barometric synthesis is found to improve the ordering of cations and to increase the value of dielectric permittivity and ion conductivity of the ceramics.

DiffractionMaterials scienceDielectricConductivityCondensed Matter PhysicsFerroelectricityElectronic Optical and Magnetic MaterialsIonsymbols.namesakeChemical engineeringvisual_artvisual_art.visual_art_mediumsymbolsCeramicRaman spectroscopySolid solutionFerroelectrics
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