Search results for "RELAXATION"

showing 10 items of 1162 documents

Dielectric investigation of lead‐free perovskite strontium titanate with 25% bismuth ceramics

2009

In this work lead-free 0.75SrTiO3-0.25BiTiO3 ceramics have been investigated in broad frequency range. Obtained results showed pronounced dispersion below room temperature typical for the dipolar glasses. The calculated relaxation time distribution function broadens toward longest relaxation times part on cooling. The obtained most probable relaxation time diverges according to the Vogel-Fulcher relationship with the following parameters: dipole activation energy EA=2123 K, glassy state temperature T0=52.7 K, shortest relaxation time, referring to dipole relaxations at very high temperatures, τ0=2.1·10–14 s. (© 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)

Condensed matter physicsChemistryRelaxation (NMR)chemistry.chemical_elementActivation energyDielectricCondensed Matter PhysicsBismuthDipolechemistry.chemical_compoundNuclear magnetic resonanceStrontium titanateDispersion (chemistry)Perovskite (structure)physica status solidi c
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Nature of the non-exponential primary relaxation in structural glass-formers probed by dynamically selective experiments

1998

Several experimental methods feature the potential to distinguish between slow and fast contributions to the non-exponential, ensemble averaged primary response in glass-forming materials. Some of these techniques are based on the selection of subensembles using multi-dimensional nuclear magnetic resonance, optical bleaching, and non-resonant spectral hole burning. Others, such as the time-dependent solvation spectroscopy, measure microscopic responses induced by local perturbations. Using several of these methods it could be demonstrated for various glass-forming materials that the non-exponential relaxation results from a superposition of dynamically distinguishable entities. The experime…

Condensed matter physicsChemistrySolvationCondensed Matter Physics530Measure (mathematics)Electronic Optical and Magnetic MaterialsExponential functionSuperposition principleChemical physicsMaterials ChemistryCeramics and CompositesSpectral hole burningRelaxation (physics)Experimental methodsSpectroscopyJournal of Non-Crystalline Solids
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Nonexponential 2H spin-lattice relaxation as a signature of the glassy state

1990

Abstract High-precision measurements of 2H spin-lattice relaxation on several molecular glass-forming liquids have been performed. As a general feature the following can be stated: At temperatures more than ten to twenty degrees above the calorimetric glass transition temperature Tg the 2H spin-lattice relaxation is exponential; below that temperature regime the relaxation is nonexponential. This crossover from exponential to nonexponential magnetization recovery implies that no common spin temperature caused by spin diffusion exists in a 2H glass. This contrasts 1H spin-lattice relaxation which is found to be strictly monoexponential throughout. The occurrence of nonexponential 2H relaxati…

Condensed matter physicsChemistrySpin–lattice relaxationGeneral Physics and AstronomyObservableCondensed Matter::Disordered Systems and Neural NetworksExponential functionMagnetizationNuclear magnetic resonanceSpin diffusionRelaxation (physics)Physical and Theoretical ChemistryGlass transitionSpin-½Chemical Physics Letters
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Quantum chemical simulations of bound hold polarons (V Mg centers) in corundum crystals

1997

The semi-empirical INDO method has been applied to the calculations of the bound hole small-radius polarons in corundum. Results for optimized atomic and electronic structure using two different approaches (molecular cluster and periodic, supercell model) are critically compared. Both models find that two-site configurations of bound hole polarons have the lowest energy (which does not exclude existence of one-site polarons also characterized by essential relaxation energies). Experimental ENDOR data on V Mg defects are discussed in the light of the calculations.

Condensed matter physicsChemistrychemistry.chemical_elementCorundumElectronic structureengineering.materialPolaronMolecular physicsIonChemical speciesAluminiumengineeringSupercell (crystal)Relaxation (physics)SPIE Proceedings
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Spin transition in [Fe(phen)2(NCS)2] - �SR study

2004

The reversible thermal spin transition which occurs in [Fe(phen)(2)(NCS)(2)] around T-1/2 similar to 177 K has been investigated by muon spin relaxation (muSR) (similar to10-280 K). The depolarisation curves are well described by two Lorentzian lines represent fast and slow components in the decay curves, with the initial asymmetry parameter of the fast component found to track the spin transition in [Fe(phen)2(NCS),]. Comparison of zero-field and transverse field (20 Oe) muSR measurements shows that diamagnetic muonic species occur over the entire temperature range.

Condensed matter physicsChemistrymedia_common.quotation_subjectRelaxation (NMR)Analytical chemistrySpin transitionAtmospheric temperature rangeMuon spin spectroscopyCondensed Matter PhysicsAsymmetryElectronic Optical and Magnetic MaterialsSpin crossoverThermalDiamagnetismmedia_commonphysica status solidi (a)
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Testing Mode-Coupling Theory for a Supercooled Binary Lennard-Jones Mixture I: The van Hove Correlation Function

1995

We report the results of a large scale computer simulation of a binary supercooled Lennard-Jones liquid. We find that at low temperatures the curves for the mean squared displacement of a tagged particle for different temperatures fall onto a master curve when they are plotted versus rescaled time $tD(T)$, where $D(T)$ is the diffusion constant. The time range for which these curves follow the master curve is identified with the $\alpha$-relaxation regime of mode-coupling theory (MCT). This master curve is fitted well by a functional form suggested by MCT. In accordance with idealized MCT, $D(T)$ shows a power-law behavior at low temperatures. The critical temperature of this power-law is t…

Condensed matter physicsCondensed Matter (cond-mat)FOS: Physical sciencesThermodynamicsCondensed MatterPower lawFick's laws of diffusionMean squared displacementCondensed Matter::Soft Condensed MatterCorrelation function (statistical mechanics)AmplitudeMode couplingRelaxation (physics)Critical exponentMathematics
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Calculations of the atomic and electronic structure for SrTiO3 perovskite thin films

2001

The results of calculations of SrTiO3 (100) surface relaxation and rumpling with two different terminations (SrO and TiO2) are presented and discussed. We have used the ab initio Hartree–Fock (HF) method with electron correlation corrections and the density functional theory (DFT) with different exchange–correlation functionals, including hybrid exchange techniques. All methods agree well on surface energies and on atomic displacements, as well as on the considerable increase of covalency effects near the surface. More detailed experiments on surface rumpling and relaxation are necessary for further testing of theoretical predictions.

Condensed matter physicsElectronic correlationChemistryMetals and AlloysAb initioSurfaces and InterfacesElectronic structureMolecular physicsSurface energySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCondensed Matter::Materials ScienceAb initio quantum chemistry methodsPhysics::Atomic and Molecular ClustersMaterials ChemistryRelaxation (physics)Density functional theoryLocal-density approximationThin Solid Films
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β-process of supercooled o-terphenyl: a comparison of dielectrical and NMR data guided by mode-coupling theory

1990

Abstract According to predictions of mode-coupling theory of the liquid-glass transition, a Cole-Cole dynamical susceptibility is applied to the β-relaxation of supercooled o -terphenyl as studied by 2 H NMR spin-lattice relaxation and by dielectrical relaxation. A temperature-dependent amplitude (1- f ) is assumed for the β-process which yields a description of the NMR data consistent with the dielectrical data. The plateau value f separating the α- and β-processes in the two-step correlation function reveals a similar temperature dependence as compared to the Debye-Waller factor.

Condensed matter physicsRelaxation (NMR)Spin–lattice relaxationGeneral Physics and AstronomyThermodynamicsNuclear magnetic resonance spectroscopychemistry.chemical_compoundMolecular dynamicsCorrelation functionchemistryTerphenylProton NMRPhysical and Theoretical ChemistrySupercoolingChemical Physics Letters
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Comparative study of [001] surface relaxations of perovskite titanates

1998

Surface relaxations of the cubic perovskite SrTiO and BaTiO crystals have been studied in the framework of the shell model. The 33 positions of atoms in several surface layers embedded into the electrostatic field of the remainder of the crystal were calculated. Ti 4q , Sr 2q ,B a 2q and O 2y ions in six near-surface layers are displaced differently from their crystalline sites. Such effects create the so-called surface rumpling, a dipole moment and the electric field in the near-surface region. Calculated atomic displacements were compared with the LEED experimental data and showed good agreement. Our simulations have demonstrated that the cubic perovskite SrTiO crystals 3 reveal surface p…

Condensed matter physicsbusiness.industryRelaxation (NMR)Metals and AlloysSurfaces and InterfacesDielectricFerroelectricitySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystalDipolechemistry.chemical_compoundOpticschemistryElectric fieldMaterials ChemistryStrontium titanatebusinessPerovskite (structure)Thin Solid Films
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Bis(2-ethylhexyl)phosphoric acid/bis(2-ethylhexyl)amine mixtures as solvent media for lithium-ions: A dynamical study

2016

Abstract The self-diffusion coefficient, the spin-lattice relaxation times and ionic conductivity of lithium ions in liquid mixtures composed of bis(2-ethylhexyl)amine (BEEA) and bis(2-ethylhexyl)phosphoric acid (HDEHP) have been thoroughly investigated as a function of composition and temperature by NMR spectroscopy and conductometry. While the temperature and composition dependence of diffusion coefficients of lithium ions follow the same trend observed for those of the surfactant molecules, the spin-lattice relaxation times of lithium ions and 1 H are remarkably different. The observed behavior has been interpreted in terms of lithium ions diffusion occurring through its association with…

ConductometrySurfactantsInorganic chemistrychemistry.chemical_element02 engineering and technology010402 general chemistrySelf-diffusion coefficients01 natural sciencesSpin-lattice relaxation timechemistry.chemical_compoundColloid and Surface ChemistryPulmonary surfactantLithium ionSpin-lattice relaxation timeSelf-diffusion coefficientsSurfactantsLithium ionMoleculeIonic conductivityPhysics::Chemical PhysicsPhosphoric acidSettore CHIM/02 - Chimica FisicaChemistryNuclear magnetic resonance spectroscopy021001 nanoscience & nanotechnology0104 chemical sciencesSolventLithium0210 nano-technology
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