Search results for "Density Functional Theory."

showing 10 items of 935 documents

Defying Stereotypes with Nanodiamonds: Stable Primary Diamondoid Phosphines

2016

International audience; Direct unequal C-H bond difunctionalization of phosphorylated diamantane was achieved in high yield from the corresponding phosphonates. Reduction of the functionalized phosphonates provides access to novel primary and secondary alkyl/aryl diamantane phosphines. The prepared primary diamantyl phosphines are quite air stable compared to their adamantyl and especially alkyl or aryl analogues. This finding is corroborated by comparing the singly occupied molecular orbital energy levels of the corresponding phosphine radical cations obtained by density functional theory computations.

room-temperaturemolecular tripoddeactivated aryl chlorideshomogeneous catalysts010402 general chemistryDiamondoidselective preparationchemistry01 natural sciencesMedicinal chemistryChemical reaction[ CHIM ] Chemical Scienceschemistry.chemical_compoundOrganic chemistry[CHIM]Chemical SciencesarylationAlkylNanodiamonds ; Diamondoid Phosphines ; diamantane ; adamantane ; adamantylphosphinechemistry.chemical_classification010405 organic chemistryChemistryligandsArylOrganic Chemistrypalladiumphosphorylated adamantanes3. Good health0104 chemical sciencesChemical bondDensity functional theoryDiamantanePhosphine
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Localized surface plasmon resonance in silver nanoparticles: Atomistic first-principles time-dependent density-functional theory calculations

2015

We observe using ab initio methods that localized surface plasmon resonances in icosahedral silver nanoparticles enter the asymptotic region already between diameters of 1 and 2 nm, converging close to the classical quasistatic limit around 3.4 eV. We base the observation on time-dependent density-functional theory simulations of the icosahedral silver clusters Ag$_{55}$ (1.06 nm), Ag$_{147}$ (1.60 nm), Ag$_{309}$ (2.14 nm), and Ag$_{561}$ (2.68 nm). The simulation method combines the adiabatic GLLB-SC exchange-correlation functional with real time propagation in an atomic orbital basis set using the projector-augmented wave method. The method has been implemented for the electron structure…

silver nanoparticlesMaterials scienceta221Ab initioFOS: Physical sciencesMetal nanoparticlesMolecular physicsAtomic orbitalTime-dependent density functional theorySurface plasmon resonanceta116ta218Basis setPlasmonCondensed Matter - Materials Scienceta214ta114Condensed matter physicsMaterials Science (cond-mat.mtrl-sci)Time-dependent density functional theoryCondensed Matter PhysicsNanoshellElectronic Optical and Magnetic MaterialsPlasmonicssurface plasmon resonanceLocalized surface plasmonPhysical Review B
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Addition of Ethylene or Hydrogen to a Main-Group Metal Cluster under Mild Conditions

2015

Reaction of the tin cluster Sn8(Arinline image)4 (Arinline image=C6H2-2,6-(C6H3-2,4,6-Me3)2) with excess ethylene or dihydrogen at 25 °C/1 atmosphere yielded two new clusters that incorporated ethylene or hydrogen. The reaction with ethylene yielded Sn4(Arinline image)4(C2H2)5 that contained five ethylene moieties bridging four aryl substituted tin atoms and one tin–tin bond. Reaction with H2 produced a cyclic tin species of formula (Sn(H)Arinline image)4, which could also be synthesized by the reaction of {(Arinline image)Sn(μ-Cl)}2 with DIBAL-H. These reactions represent the first instances of direct reactions of isolable main-group clusters with ethylene or hydrogen under mild conditions…

small molecule activationEthyleneHydrogenInorganic chemistrychemistry.chemical_elementInfrared spectroscopyCatalysisetyleeniklusteritchemistry.chemical_compoundtinPolymer chemistryCluster (physics)ethyleneclustersta116ArylmetalliklusteritGeneral ChemistryGeneral MedicinechemistryMain group elementvetyhydrogenpienmolekyylien aktivointiDensity functional theorytinaTinAngewandte Chemie
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Gallium preference for the occupation of tetrahedral sites in Lu3(Al5-xGax)O12multicomponent garnet scintillators according to solid-state nuclear ma…

2019

Abstract In this study, the distributions of aluminum and gallium atoms over the tetrahedral and octahedral sites in the garnet structure were investigated in mixed Lu3Al5-xGaxO12 crystals by using 27Al and 71Ga magic angle spinning nuclear magnetic resonance (NMR) and single crystal 71Ga NMR. The experimental study was supported by theoretical calculations based on density functional theory (DFT) in order to predict the trends in terms of the substitutions of Al by Ga in the mixed garnets. Both the experimental and theoretical results indicated the non-uniform distribution of Al and Ga over the tetrahedral and octahedral sites in the garnet structure, with a strong preference for Ga occupy…

spectroscopyIonic radiusMaterials scienceRelaxation (NMR)chemistry.chemical_element02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesCrystallographyChemical bondchemistrySolid-state nuclear magnetic resonanceSolid-state nuclear magnetic resonanceMagic angle spinningGeneral Materials ScienceDensity functional theoryLu3Al5-xGaxO12Gallium0210 nano-technologydensity functional theory calculationSingle crystalJournal of Physics and Chemistry of Solids
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Octopus, a computational framework for exploring light-driven phenomena and quantum dynamics in extended and finite systems

2020

Over the last few years, extraordinary advances in experimental and theoretical tools have allowed us to monitor and control matter at short time and atomic scales with a high degree of precision. An appealing and challenging route toward engineering materials with tailored properties is to find ways to design or selectively manipulate materials, especially at the quantum level. To this end, having a state-of-the-art ab initio computer simulation tool that enables a reliable and accurate simulation of light-induced changes in the physical and chemical properties of complex systems is of utmost importance. The first principles real-space-based Octopus project was born with that idea in mind,…

spectroscopyPhotonelectronic-structure calculationsComputer sciencespectraQuantum dynamicsmolecular-dynamicsComplex systemGeneral Physics and AstronomyFOS: Physical sciences010402 general chemistryspin01 natural sciencesSettore FIS/03 - Fisica Della MateriaEngineeringTDDFTreal-space0103 physical sciencesoctopusgeneralized gradient approximationPhysical and Theoretical Chemistrydensity-functional theoryMassively parallelQuantumChemical Physicsreal time010304 chemical physicsComputational Physics (physics.comp-ph)scientific software0104 chemical sciencestotal-energy calculationsphysics.comp-phPhysical SciencesChemical Sciencespolarizable continuum modelState of matterSystems engineeringLight drivenDensity functional theoryPhysics - Computational Physics
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Spin caloric transport from density-functional theory

2019

Spin caloric transport refers to the coupling of heat with spin transport. Its applications primarily concern the generation of spin currents and control of magnetisation by temperature gradients for information technology, known by the synonym spin caloritronics. Within the framework of ab initio theory, new tools are being developed to provide an additional understanding of these phenomena in realistic materials, accounting for the complexity of the electronic structure without adjustable parameters. Here, we review this progress, summarising the principles of the density-functional-based approaches in the field and presenting a number of application highlights. Our discussion includes th…

spintronicsMaterials scienceAcoustics and UltrasonicsSpintronicsCondensed matter physicsthermal spin torqueCaloric theory02 engineering and technologyPhysik (inkl. Astronomie)021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesspin Nernst effectSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialsspin Seebeck effectdensity functional calculations0103 physical sciencesspin caloritronicsDensity functional theoryCondensed Matter::Strongly Correlated Electronsmagneto-Seebeck effect010306 general physics0210 nano-technologySpin-½
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Copper-hydride nanoclusters with enhanced stability by N-heterocyclic carbenes

2021

AbstractCopper-hydrides have been intensively studied for a long time due to their utilization in a variety of technologically important chemical transformations. Nevertheless, poor stability of the species severely hinders its isolation, storage and operation, which is worse for nano-sized ones. We report here an unprecedented strategy to access to ultrastable copper-hydride nanoclusters (NCs), namely, using bidentate N-heterocyclic carbenes as stabilizing ligands in addition to thiolates. In this work, a simple synthetic protocol was developed to synthesize the first large copper-hydride nanoclusters (NCs) stabilized by N-heterocyclic carbenes (NHCs). The NC, with the formula of Cu31(RS)2…

superatomMaterials scienceSuperatomkuparistabilityCondensed Matter PhysicsAtomic and Molecular Physics and OpticsFourier transform ion cyclotron resonancecopper-hydrideNanoclustersN-heterocylic carbeneCrystallographychemistry.chemical_compoundklusteritUltraviolet visible spectroscopymetal clusterschemistryCluster (physics)Copper hydrideGeneral Materials ScienceThermal stabilityDensity functional theorynanohiukkasetElectrical and Electronic Engineering
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Thiol-Stabilized Atomically Precise, Superatomic Silver Nanoparticles for Catalyzing Cycloisomerization of Alkynyl Amines

2018

Abstract Both the electronic and surface structures of metal nanomaterials play critical roles in determining their chemical properties. However, the non-molecular nature of conventional nanoparticles makes it extremely challenging to understand the molecular mechanism behind many of their unique electronic and surface properties. In this work, we report the synthesis, molecular and electronic structures of an atomically precise nanoparticle, [Ag206L72]q (L = thiolate, halide; q = charge). With a four-shell Ag7@Ag32@Ag77@Ag90 Ino-decahedral structure having a nearly perfect D5h symmetry, the metal core of the nanoparticle is co-stabilized by 68 thiolate and 4 halide ligands. Both electroche…

superatomMaterials sciencemetal nanoclustersatomically precise nanoparticlesNanoparticle02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesSilver nanoparticleNanomaterialsCycloisomerizationjalometallitReactivity (chemistry)ta116PlasmonMultidisciplinaryta114Superatom021001 nanoscience & nanotechnologynanocatalysisnobel metal0104 chemical sciencesDensity functional theorynanohiukkaset0210 nano-technologyNational Science Review
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Constant inner potential DFT for modelling electrochemical systems under constant potential and bias

2021

Electrochemical interfaces and reactions play a decisive role in e.g. clean energy conversion but understanding their complex chemistry remains an outstanding challenge. Constant potential or grand canonical ensemble (GCE) simulations are indispensable for unraveling the properties of electrochemical processes as a function of the electrode potential. Currently, constant electrode potential calculations at the density functional theory (DFT) level are carried out by fixing the Fermi level of the simulation cell. However, the Fermi level from DFT calculations does does not always reflect the experimentally controlled electrode potential or describe the thermodynamic independent variable in G…

symbols.namesakeGrand canonical ensembleMaterials scienceChemical physicsFermi levelsymbolsDensity functional theoryConstant (mathematics)ElectrocatalystForce field (chemistry)Electrode potentialElectrochemical potential
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Uncertainty analysis and symmetry restoration in nuclear self-consistent methods

2015

This thesis contains two articles, in the following denoted by I and II, and an introduction to them. In Chapter 1, I present the theoretical models of nuclear structure. In Chapter 2, I introduce the basic ideas about the density functional theory (DFT) and self-consistent mean-field (SCMF) calculations. In Chapter 3, I give the formulae for the uncertainty propagation, which is the error analysis method used in article I. As a proper tool to survey the predictive power of theoretical models, the error analysis now has become more and more widely used. By analyzing the propagation of uncertainties, one tries to find out the e ectiveness of the calculation with a given parameter set obtaine…

symmetriaydinrakenneenergiatiheysfunktionaalitnuclear density functional theorytiheysfunktionaaliteorianuclear structurepropagation of uncertaintyenergy-density-functionalssymmetry restorationmatemaattiset mallitydinfysiikkavirheanalyysi
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