Search results for "CALCULATIONS"

showing 10 items of 468 documents

Density functional theory based screening of ternary alkali-transition metal borohydrides: a computational material design project.

2009

We present a computational screening study of ternary metal borohydrides for reversible hydrogen storage based on density functional theory. We investigate the stability and decomposition of alloys containing 1 alkali metal atom, Li, Na, or K M1; and 1 alkali, alkaline earth or 3d / 4d transition metal atom M2 plus two to five BH4  groups, i.e., M1M2BH42‐5, using a number of model structures with trigonal, tetrahedral, octahedral, and free coordination of the metal borohydride complexes. Of the over 700 investigated structures, about 20 were predicted to form potentially stable alloys with promising decomposition energies. The M1Al/ Mn/ FeBH44, Li/ NaZnBH43, and Na/ KNi/ CoBH43 alloys are …

Inorganic chemistryGeneral Physics and Astronomy02 engineering and technologyab initio calculations ; aluminium alloys ; boron alloys ; cobalt alloys ; decomposition ; density functional theory ; electronic structure ; hydrogen ; hydrogen storage ; iron alloys ; lithium alloys ; manganese alloys ; nickel alloys ; niobium alloys ; potassium alloys ; rhodium alloys ; sodium alloys ; thermodynamics ; zinc alloysMaterialeforskning010402 general chemistryBorohydride01 natural sciences7. Clean energyMetalHydrogen storagechemistry.chemical_compoundMaterials and systems for energy storageTransition metalAb initio quantum chemistry methodsMaterialer og systemer til energilagringPhysical and Theoretical ChemistryMaterials research021001 nanoscience & nanotechnologyAlkali metal0104 chemical scienceschemistryvisual_artvisual_art.visual_art_mediumPhysical chemistryDensity functional theory0210 nano-technologyTernary operationThe Journal of chemical physics
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Wannier90 as a community code: new features and applications

2019

Wannier90 is an open-source computer program for calculating maximally-localised Wannier functions (MLWFs) from a set of Bloch states. It is interfaced to many widely used electronic-structure codes thanks to its independence from the basis sets representing these Bloch states. In the past few years the development of Wannier90 has transitioned to a community-driven model; this has resulted in a number of new developments that have been recently released in Wannier90 v3.0. In this article we describe these new functionalities, that include the implementation of new features for wannierisation and disentanglement (symmetry-adapted Wannier functions, selectively-localised Wannier functions, s…

Interface (Java)02 engineering and technologysemiconductors01 natural sciencesGeneral Materials Sciencefieldslocal orbitalCondensed Matter - Materials ScienceUnit testingComputer programBasis (linear algebra)electronstooldynamicsComputational Physics (physics.comp-ph)021001 nanoscience & nanotechnologyCondensed Matter Physicsspin polarizationreal-space methods[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]0210 nano-technologyPhysics - Computational PhysicspseudopotentialsconstructionMaterials sciencelocal orbitalsFluids & Plasmasreal-space method0204 Condensed Matter PhysicsFOS: Physical sciencesComputational sciencecrystalSet (abstract data type)band structure interpolation0103 physical sciencesddc:530Wannier function010306 general physics0912 Materials Engineeringdensity-functional theoryWannier orbitalWannier function1007 Nanotechnologybusiness.industrywannier orbitalsMaterials Science (cond-mat.mtrl-sci)Usabilitywannier functionsWannier functions; band structure interpolation; local orbitals; real-space methods; electronic structure; Wannier orbitals; density-functional theoryelectronic structureAutomationtotal-energy calculationsbusiness
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N-heterocyclic carbenes and parent cations: acidity, nucleophilicity, stability, and hydrogen bonding-Electrochemical Study and ab initio calculations

2016

N-Heterocyclic carbenes (NHCs) are widely used as organocatalysts. Their reactivity (and instability) is related to their basicity and nucleophilicity, which, in turn, are linked to their scaffold. NHCs can be generated by chemical deprotonation or electrochemical reduction of the parent azolium cations, NHCH+s. Cyclic voltammetry enabled the reduction potential of the NHCH+s to be determined; the reduction potential is related to the acidity of the NHCH+s and the oxidation potential of the NHCs, which is related to the nucleophilicity of the NHCs. It was thus possible to order different NHCH+s and NHCs by their acidity and nucleophilicity, respectively. A study on the stability of NHCs was…

Ionic liquids electrochemistry ab initio calculations010405 organic chemistryHydrogen bondChemistrySettore CHIM/06 - Chimica Organica010402 general chemistryElectrochemistry01 natural sciencesMedicinal chemistryCatalysis0104 chemical sciencesCatalysisDeprotonationNucleophileAb initio quantum chemistry methodsComputational chemistrySettore CHIM/03 - Chimica Generale E InorganicaElectrochemistryReactivity (chemistry)Cyclic voltammetry
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Two C3-symmetric Dy3 III complexes with triple di-μ-methoxo-μ-phenoxo bridges, magnetic ground state, and single-molecule magnetic behavior

2014

Two series of isostructural C3-symmetric Ln3 complexes Ln3·[BPh4] and Ln3·0. 33[Ln(NO3)6] (in which LnIII=Gd and Dy) have been prepared from an amino-bis(phenol) ligand. X-ray studies reveal that LnIII ions are connected by one μ2-phenoxo and two μ3-methoxo bridges, thus leading to a hexagonal bipyramidal Ln3O5 bridging core in which LnIII ions exhibit a biaugmented trigonal-prismatic geometry. Magnetic susceptibility studies and ab initio complete active space self-consistent field (CASSCF) calculations indicate that the magnetic coupling between the DyIII ions, which possess a high axial anisotropy in the ground state, is very weakly antiferromagnetic and mainly dipolar in nature. To redu…

LanthanideGadoliniumab initio calculationsOrganic Chemistrychemistry.chemical_elementGadoliniumGeneral ChemistryCatalysisCrystallographychemistryComputational chemistryAb initio quantum chemistry methodsMagnetic propertiesLanthanidesDysprosiumDysprosiumMoleculeGround stateta116Chemistry: A European Journal
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Size-intensive decomposition of orbital energy denominators

2000

We introduce an alternative to Almlöf and Häser’s Laplace transform decomposition of orbital energy denominators used in obtaining reduced scaling algorithms in perturbation theory based methods. The new decomposition is based on the Cholesky decomposition of positive semidefinite matrices. We show that orbital denominators have a particular short and size-intensive Cholesky decomposition. The main advantage in using the Cholesky decomposition, besides the shorter expansion, is the systematic improvement of the results without the penalties encountered in the Laplace transform decomposition when changing the number of integration points in order to control the convergence. Applications will…

Laplace transformIntegrationGeneral Physics and AstronomyMinimum degree algorithmOrbital calculations ; Perturbation theory ; Convergence of numerical methods ; Integration ; Coupled cluster calculationsPositive-definite matrixPerturbation theoryUNESCO::FÍSICA::Química físicaOrbital calculationsSpecific orbital energyPhysics and Astronomy (all)Coupled cluster calculationsComputational chemistryConvergence (routing)Decomposition (computer science)Convergence of numerical methodsApplied mathematicsPhysical and Theoretical ChemistryPerturbation theory:FÍSICA::Química física [UNESCO]Cholesky decompositionMathematics
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Multi-scale dynamics simulations of molecular polaritons: The effect of multiple cavity modes on polariton relaxation

2021

It is included two versions of this item: the Accepted Version which is already Open Access and the Published Version which is under an embargo period till 2022-03-09.

LightPhysics::OpticsGeneral Physics and AstronomyMolecular dynamics010402 general chemistry01 natural sciencesMolecular physicsquantum mechanical/molecular mechanical calculationsdark stateslaw.inventionMolecular dynamicslaw0103 physical sciencesDispersion (optics)kvanttikemiaPolaritonmolekyylidynamiikkaWave vectorPhysical and Theoretical ChemistryfotoluminesenssipolaritonitPhotoluminescence010304 chemical physicsFísicaCalculationMoleculesRay0104 chemical sciencesMirrorsCoupling (physics)Dark stateOptical cavitymolecular propertiesQuantum chemistryatomistic simulationsThe Journal of Chemical Physics
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Pharmacogenetic Study of ABCB1 and CYP3A5 Genes During the First Year Following Heart Transplantation Regarding Tacrolimus or Cyclosporine Levels

2011

Pharmacogenetics explains part of the interindividual variability in drug responses. Many published works about the effects of single nucleotide polymorphisms (SNPs) on immunosuppressive drug blood levels present contradictory results. We evaluated the SNPs in ABCB1 (glycoprotein P) and CYP3A5 (metabolic enzyme) genes, seeking correlate them with tacrolimus or cyclosporine levels during the first year after heart transplantation. One blood sample was obtained from each of 41 patients: 26 treated with cyclosporine and 15 with tacrolimus. We characterize the SNPs rs1045642, 1128503, 2032582, 2235013, 2235033, 2229109, 3213619, 9282564 in ABCB1 and rs10264272, 776746 in CYP3A5 genes using the …

Linkage disequilibriummedicine.medical_specialtyATP Binding Cassette Transporter Subfamily BGenotypemedicine.medical_treatmentSingle-nucleotide polymorphismBiologyPharmacologyPolymorphism Single NucleotideGastroenterologyLinkage DisequilibriumTacrolimusGene FrequencyInternal medicineGenotypemedicineCytochrome P-450 CYP3AHumansDrug Dosage CalculationsATP Binding Cassette Transporter Subfamily B Member 1CYP3A5Heart transplantationTransplantationTacrolimusPhenotypeImmunosuppressive drugPharmacogeneticsSpainCyclosporineHeart TransplantationSurgeryDrug MonitoringImmunosuppressive AgentsPharmacogeneticsTransplantation Proceedings
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Resistance simulations for junctions of SW and MW carbon nanotubes with various metal substrates

2011

Abstract This theoretical study focuses on junctions between the carbon nanotubes (CNTs) and contacting metallic elements of a nanocircuit. Numerical simulations on the conductance and resistance of these contacts have been performed using the multiple scattering theory and the effective media cluster approach. Two models for CNT-metal contacts have been considered in this paper: a) first principles “liquid metal” model and b) semi-empirical model of “effective bonds” based on Landauer notions on ballistic conductivity. Within the latter, which is a more adequate description of chirality effects, we have simulated both single-wall (SW) and multi-wall (MW) CNTs with different morphology. Res…

Liquid metalMaterials scienceelectronic structure calculationsQC1-999General Physics and AstronomyNanotechnology02 engineering and technologyCarbon nanotubeConductivity01 natural sciencesMolecular physicslaw.inventionMetallaw0103 physical sciencesCluster (physics)010306 general physicsscattering theorycarbon nanotubesjunction between the cnt and metal substrateresistance of cnt-me contactPhysicsinter-wall transparency in mw cntsConductance021001 nanoscience & nanotechnologysw and mw morphologyvisual_artvisual_art.visual_art_mediumScattering theory0210 nano-technologyChirality (chemistry)Central European Journal of Physics
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Radiopurity control in the NEXT-100 double beta decay experiment: procedures and initial measurements

2013

[EN] The "Neutrino Experiment with a Xenon Time-Projection Chamber" (NEXT) is intended to investigate the neutrinoless double beta decay of Xe-136, which requires a severe suppression of potential backgrounds. An extensive screening and material selection process is underway for NEXT since the control of the radiopurity levels of the materials to be used in the experimental set-up is a must for rare event searches. First measurements based on Glow Discharge Mass Spectrometry and gamma-ray spectroscopy using ultra-low background germanium detectors at the Laboratorio Subterraneo de Canfranc (Spain) are described here. Activity results for natural radioactive chains and other common radionucl…

MECANICA DE LOS MEDIOS CONTINUOS Y TEORIA DE ESTRUCTURASPhysics - Instrumentation and DetectorsGlow Discharge Mass SpectrometryPhysics::Instrumentation and Detectorschemistry.chemical_elementFOS: Physical sciencesGermanium01 natural sciences7. Clean energyTECNOLOGIA ELECTRONICANuclear physicsCambres d'ionitzacióXenonDouble beta decay0103 physical sciencesNuclear Experiment (nucl-ex)010306 general physicsNuclear ExperimentInstrumentationDetectors de radiacióMathematical PhysicsPhysicsRadionuclideRadiation calculationsIonization chambers010308 nuclear & particles physicsTime projection Chambers (TPC)Gamma detectors (scintillators CZT HPG HgI etc)FísicaInstrumentation and Detectors (physics.ins-det)chemistryNuclear countersNeutrino
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Solution structure of R2Sn(IV)-β-N-Acetyl-Neuraminate (R=Me, Bu) complexes in D2O and DMSO-d6: experimental NMR and DFT computational study.

2007

Two diorganotin(IV)-NANA complexes (NANA (1) = beta-N-acetyl-Neuraminic Acid = 5-amino-3,5-dideoxy-D-glycero-beta-D-galactononulosic acid) with formula Me(2)Sn(iv)NANA (2) and Bu(2)Sn(IV)NANA (3) were synthesized and characterized by (1)H, (13)C and (119)Sn NMR spectroscopy, both in D(2)O and DMSO-d(6) solutions. The experimental data in DMSO suggested the monosaccharide bidentate chelation via O1 carboxylate and vicinal O2 alkoxide atoms, which, in D(2)O, can be dynamically extended to a third binding site (O8 atom) of the pendant chain. Coordination at the tin atom is discussed on the basis of experimental NMR data and DFT calculation.

Magnetic Resonance SpectroscopyDenticityMolecular StructureStereochemistrychemistry.chemical_elementNuclear magnetic resonance spectroscopyMedicinal chemistrySolutionsInorganic Chemistrychemistry.chemical_compoundchemistryAlkoxideOrganotin CompoundsSialic AcidsSide chainDimethyl SulfoxideNeuraminic AcidsChelationCarboxylateNMR structural characterization; Alkyltin(IV); N-acetilneuraminic acid; DFT theroretical calculationsDeuterium OxideTinMathematical ComputingVicinalNMR DFT sialic acid
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