Search results for "physical chemistry"

showing 10 items of 1199 documents

Oxygen and vacancy defects in silicon. A quantum mechanical characterization through the IR and Raman spectra.

2021

The Infrared (IR) and Raman spectra of various defects in silicon, containing both oxygen atoms (in the interstitial position, Oi) and a vacancy, are computed at the quantum mechanical level by using a periodic supercell approach based on a hybrid functional (B3LYP), an all-electron Gaussian-type basis set, and the Crystal code. The first of these defects is VO: the oxygen atom, twofold coordinated, saturates the unpaired electrons of two of the four carbon atoms on first neighbors of the vacancy. The two remaining unpaired electrons on the first neighbors of the vacancy can combine to give a triplet (Sz = 1) or a singlet (Sz = 0) state; both states are investigated for the neutral form of …

Materials science010304 chemical physicsGeneral Physics and AstronomyInfrared spectroscopy010402 general chemistry01 natural sciencesMolecular physics0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCrystalsymbols.namesakeUnpaired electronVacancy defect0103 physical sciencessymbolsSinglet statePhysical and Theoretical ChemistryGround stateRaman spectroscopyComputingMilieux_MISCELLANEOUSBasis setThe Journal of chemical physics
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The heat of transfer in a chemical reaction at equilibrium.

2007

International audience; We study a reacting mixture (2F $ F2) in a temperature gradient. We had previously used boundary-driven non-equilibrium molecular dynamics (NEMD) simulations to study this system, and found that the reaction was close to local chemical equilibrium in temperature gradients up to 1012 K/m. Using the condition of local chemical equilibrium, we show that the heat of transfer of the reacting mixture is equal to minus the enthalpy of the reaction. The fact that the sign of the heat of transfer is determined by the type of reaction adds insight to the discussion of the origin of the sign

Materials science010304 chemical physicsGeneral Physics and AstronomyThermodynamics02 engineering and technologyGeneral Chemistry021001 nanoscience & nanotechnology01 natural sciencesReaction quotient[PHYS.PHYS.PHYS-CHEM-PH] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Law of mass actionReaction rate[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistryChemical clock[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Equilibrium thermodynamicsTemperature jump0103 physical sciences[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistry[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Chemical equilibrium0210 nano-technologyEquilibrium constantComputingMilieux_MISCELLANEOUS
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Interstitial carbon defects in silicon. A quantum mechanical characterization through the infrared and Raman spectra.

2021

The infrared (IR) and Raman spectra of eight substitutional carbon defects in silicon are computed at the quantum mechanical level by using a periodic supercell approach based on hybrid functionals, an all electron Gaussian type basis set and the CRYSTAL code. The single substitutional C s case and its combination with a vacancy (C s V and C s SiV) are considered first. The progressive saturation of the four bonds of a Si atom with C is then examined. The last set of defects consists of a chain of adjacent carbon atoms C s i , with i = 1-3. The simple substitutional case, C s , is the common first member of the three sets. All these defects show important, very characteristic features in th…

Materials science010304 chemical physicsSiliconInfrared spectroscopychemistry.chemical_elementGeneral ChemistryElectronic structure010402 general chemistry01 natural sciencesMolecular physics0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCrystalComputational Mathematicssymbols.namesakechemistryVacancy defect0103 physical sciencesAtomsymbolsRaman spectroscopyComputingMilieux_MISCELLANEOUSBasis setJournal of computational chemistryREFERENCES
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Co-doping with boron and nitrogen impurities in T-carbon

2020

Previously, Ren et al. [Chem. Phys. 518, 69–73, 2019] reported the failure of Boron-Nitrogen (B-N) co-doping as inter B-N bond in T-carbon. In present work, a B-N atom pair is introduced in T-carbon as p-n co-dopant to substitute two carbon atoms in the same carbon tetrahedron and form an intra B-N bond. The stability of this doping system is verified from energy, lattice dynamic, and thermodynamic aspects. According to our B3PW calculations, B-N impurities in this situation can reduce the band gap of T-carbon from 2.95 eV to 2.55 eV, making this material to be a promising photocatalyst. Through the study of its transport properties, we can also conclude that B-N co-doping cannot improve th…

Materials science010405 organic chemistryBand gapDopingT-carbonchemistry.chemical_elementGeneral Chemistry010402 general chemistryDFT01 natural sciencesNitrogen0104 chemical scienceslcsh:Chemistrylcsh:QD1-999chemistryImpurityLattice (order)AtomThermoelectric effect:NATURAL SCIENCES:Physics [Research Subject Categories]DopingPhysical chemistryBN pairBoronJournal of Saudi Chemical Society
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Searching for new borondifluoride β -diketonate complexes with enhanced absorption/emission properties using ab initio tools

2018

International audience; The rational design of fluorophores with enhanced absorption/emission properties increasingly relies on theoretical chemistry, as new ab initio methods suited for electronically excited-states reduce the gap between calculated and experimental results. In this framework, Time-Dependent Density Functional Theory (TD-DFT) emerges as an attractive option as it often provides accurate results at a moderate computational cost. Here, we perform a TD-DFT-SOS-CIS(D) study of a panel of 18 borondifluoride β-diketonate complexes that can be classified as: curcuminoids, hemicurcuminoids, their ethynylene analogues, and 2′-hydroxy-chalcones. First, we reproduce the experimental …

Materials science010405 organic chemistryProcess Chemistry and TechnologyGeneral Chemical EngineeringRational designAb initio010402 general chemistry01 natural sciencesMolecular physics0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryBathochromic shiftTheoretical chemistryDensity functional theorySolvent effectsMaximaAbsorption (electromagnetic radiation)
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Comparison of conventional and dense dispersion managed systems for 160 Gb/s transmissions

2006

International audience; In this paper, we carry out, by numerical simulations and experiments on recirculating loop.. a comparative analysis of the performances of two types of dispersion management techniques for 160 Gb/s transmission systems, which correspond to short-period dispersion maps (dense dispersion management) and long-period dispersion maps (conventional dispersion management), respectively. We show that the dense dispersion management system suffers performance degradation by the effects of polarization mode dispersion (PMD) and fiber splicing losses, in a more dramatic manner than in the system with long-period map. We experimentally find that, at constant PMD, dense dispersi…

Materials science02 engineering and technology01 natural sciences010309 optics020210 optoelectronics & photonicsOptics0103 physical sciencesFusion splicingDispersion (optics)0202 electrical engineering electronic engineering information engineeringModal dispersionElectrical and Electronic EngineeringPhysical and Theoretical Chemistry[PHYS.PHYS.PHYS-AO-PH]Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]business.industryTransmission systemAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic Materials[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistry[ PHYS.PHYS.PHYS-AO-PH ] Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]Transmission (telecommunications)Polarization mode dispersion[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryDispersion managedbusiness
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Dispersion and Stabilization of Exfoliated Graphene in Ionic Liquids.

2019

The liquid-phase exfoliation of graphite is one of the most promising methods to increase production and commercial availability of graphene. Because ionic liquids can be easily obtained with chosen molecular structures and tuneable physicochemical properties, they can be use as media to optimise the exfoliation of graphite. The under- standing of the interactions involved between graphite and various chemical functions in the solvent ions will be helpful to find liquids capable of dissociating and stabilising im- portant quantities of large graphene layers. After a step of sonication, as a mechanical precursor, samples of suspended exfoliated graphene in different ionic liquids have been c…

Materials science02 engineering and technology010402 general chemistry01 natural sciencesIonlaw.inventionionic liquidslcsh:Chemistrychemistry.chemical_compoundlawsuspensionGraphiteAlkylComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationgraphiteGraphenegrapheneCorrectionGeneral Chemistryexfoliation021001 nanoscience & nanotechnologyExfoliation joint0104 chemical sciencesDielectric spectroscopy[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryChemistrylcsh:QD1-999chemistryChemical engineeringIonic liquid0210 nano-technologyTrifluoromethanesulfonate
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Molecular Selectivity of CO–N 2 Mixed Hydrates: Raman Spectroscopy and GCMC Studies

2020

This paper reports a novel quantitative investigation concerning the CO selectivity properties for mixed CO–N2 hydrates. The study was developed by combining Raman scattering experiments and grand ...

Materials science02 engineering and technology[CHIM.MATE]Chemical Sciences/Material chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialssymbols.namesakeGeneral Energy[SDU]Sciences of the Universe [physics]symbols[CHIM]Chemical SciencesPhysical chemistryPhysical and Theoretical Chemistry0210 nano-technologySelectivityRaman spectroscopyRaman scatteringComputingMilieux_MISCELLANEOUS
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A Mechanical–Electrochemical Approach for the Determination of Precursor Sites for Pitting Corrosion at the Microscale

2006

International audience; The influence of metallurgical defects and residual surface stresses generated by polishing on the pitting susceptibility of duplex stainless steels was studied by combining macro- and microelectrochemical measurements with thermal-mechanical simulation and metallography tests. It has been shown that pits initiate in both phases at metallurgical point defects (such as oxide inclusions in the ferrite and dislocation lines in the austenite). By contrast, the surface stress state was the driving force for pit initiation along the austenite/ferrite interface. Experiments at the macroscale revealed that this process represents about 40% of the total number of pits observe…

Materials science020209 energyOxidePolishing02 engineering and technologychemistry.chemical_compoundFerrite (iron)0202 electrical engineering electronic engineering information engineeringMaterials ChemistryElectrochemistryPitting corrosionAusteniteRenewable Energy Sustainability and the EnvironmentSurface stressMetallurgy021001 nanoscience & nanotechnologyCondensed Matter PhysicsCrystallographic defectSurfaces Coatings and FilmsElectronic Optical and Magnetic Materials[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry13. Climate action[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryMetallography0210 nano-technologyJournal of The Electrochemical Society
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Influence of the focusing effect on XAFS in ReO3, WO3−x and FeF3

1995

Abstract The role of the focusing effect in the formation of X-ray absorption fine structure (XAFS) is considered for ReO3, non-stoichiometric tungsten oxides WO3−x and FeF3 having the perovskite-type structure. Two cases are mainly discussed: (1) an admixture of rhenium and tungsten L2-edge XAFS in ReO3 and WO3−x crystals to the one above rhenium and tungsten L1-edge and (2) high-order superfocusing effect in Fe0F1Fe2F3Fe4 atomic chain in iron K-edge XAFS of FeF3 which is analysed using an ab initio multiple-scattering approach.

Materials scienceAbsorption spectroscopyAb initiochemistry.chemical_elementTungstenRheniumCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsX-ray absorption fine structurechemistry.chemical_compoundTungstatechemistryAb initio quantum chemistry methodsPhysical chemistryElectrical and Electronic EngineeringAbsorption (chemistry)Physica B: Condensed Matter
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