Search results for "tiheysfunktionaaliteoria"

showing 10 items of 99 documents

Thouless-Valatin Rotational Moment of Inertia from the Linear Response Theory

2017

Spontaneous breaking of continuous symmetries of a nuclear many-body system results in appearance of zero-energy restoration modes. Such modes introduce a non-physical contributions to the physical excitations called spurious Nambu-Goldstone modes. Since they represent a special case of collective motion, they are sources of important information about the Thouless-Valatin inertia. The main purpose of this work is to study the Thouless-Valatin rotational moment of inertia as extracted from the Nambu-Goldstone restoration mode that results from the zero-frequency response to the total angular momentum operator. We examine the role and effects of the pairing correlations on the rotational cha…

Angular momentumNuclear Theorymedia_common.quotation_subjectNuclear TheoryFOS: Physical sciencesRotary inertiaInertia114 Physical sciences01 natural sciencesbinding energy and massesMoment of inertia factorNuclear Theory (nucl-th)symbols.namesake0103 physical sciences010306 general physicsRotational partition functionEuler's equationsEQUATIONSmedia_commonPhysicsta114nuclear density functional theory010308 nuclear & particles physicstiheysfunktionaaliteoriacollective modelsMoment of inertianuclear structure and decayssuprajuoksevuusRotational energyClassical mechanicssuperfluiditysymbolsydinfysiikka
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Screening the bulk properties and reducibility of Fe-doped Mn2O3 from first principles calculations

2017

Abstract Manganese oxides, particularly Mn 2 O 3 , have demonstrated great potential for oxygen carrier materials in chemical looping applications. The application of these materials in the industrial scale is hindered by thermodynamic restrictions related to the reoxidation process. This disadvantage can be overcome by doping the oxide with a guest cation. Iron is one of the most promising dopants, but the atomic-level understanding of its effects on the properties of α-Mn 2 O 3 is incomplete. Herein, we report a systematic GGA+U study of the bulk properties and reducibility of Fe x Mn 2-x O 3 (0 ≤ x ≤ 2) as a function of Fe dopant concentration. In particular, we focus on a representative…

Band gapOxidechemistry.chemical_elementNanotechnology02 engineering and technologyManganeseBulk010402 general chemistry01 natural sciencesOxygenCatalysisCatalysischemistry.chemical_compoundta116density functional theoryFe dopantsDopantta114ChemistrytiheysfunktionaaliteoriaDopingOxygen transportGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesMn2O3Physical chemistry0210 nano-technologyCatalysis Today
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Spectroscopic, crystal structural, theoretical and biological studies of phenylacetohydrazide Schiff base derivatives and their copper complexes

2020

Two phenylacetohydrazide Schiff base derivatives: N’-(1-(2-hydroxyphenyl)ethylidene)-2-phenylacetohydrazide, HL1, and N’-((1-hydroxynaphthalen-2-yl)methylene)-2-phenylacetohydrazide, HL2, were synthesized. HL1 dimerizes in presence of HCl, probably via radical mechanism to give (2,2’-((1E)-hydrazine-1,2-diylidenebis(ethan-1-yl-1-ylidene))diphenol (DIM). Thermal reactions of Cu(II) ions with the two Schiff base ligands resulted in formation of the binuclear complexes [(CuL1)2] and [(CuL2)2]. The stoichiometry and structures of the reported compounds were investigated by several spectroscopic and analytical techniques. The structure of the HL1 ligand and its complex [(CuL1)2] as well as the D…

CT-DNA bindingantioxidant activitychemistry.chemical_elementkupari010402 general chemistry01 natural sciencesAnalytical ChemistryInorganic Chemistrykemialliset sidoksetchemistry.chemical_compoundDFT studiesReactivity (chemistry)copper complexesMethyleneSpectroscopyantioksidantitSchiff base010405 organic chemistryLigandtiheysfunktionaaliteoriaOrganic Chemistrymolecular dockingkompleksiyhdisteetCopper0104 chemical sciencesCrystallographyMolecular geometrychemistrySingle crystalröntgenkristallografiaStoichiometryX-ray analysisJournal of Molecular Structure
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Anion-driven encapsulation of cationic guests inside pyridine[4]arene dimers

2019

Pyridine[4]arenes have previously been considered as anion binding hosts due to the electron-poor nature of the pyridine ring. Herein, we demonstrate the encapsulation of Me4N+ cations inside a dimeric hydrogen-bonded pyridine[4]arene capsule, which contradicts with earlier assumptions. The complexation of a cationic guest inside the pyridine[4]arene dimer has been detected and studied by multiple gas-phase techniques, ESI-QTOF-MS, IRMPD, and DT-IMMS experiments, as well as DFT calculations. The comparison of classical resorcinarenes with pyridinearenes by MS and NMR experiments reveals clear differences in their host–guest chemistry and implies that cation encapsulation in pyridine[4]arene…

Cation bindingmassaspektrometriaanionitDimerpyridinearenes010402 general chemistryDFT calculations01 natural sciencesFull Research Paperdft calculationsIonlcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryPolymer chemistryPyridinesupramolekulaarinen kemiaresorcinarenesInfrared multiphoton dissociationcation bindingAnion bindinglcsh:Science010405 organic chemistryChemistrytiheysfunktionaaliteoriaOrganic ChemistryCationic polymerizationkationit5470104 chemical sciences3. Good healthChemistryion mobility mass spectrometrymacrocycleslcsh:QBeilstein Journal of Organic Chemistry
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Real-time time-dependent density functional theory implementation of electronic circular dichroism applied to nanoscale metal–organic clusters

2020

| openaire: EC/H2020/838996/EU//RealNanoPlasmon Electronic circular dichroism (ECD) is a powerful spectroscopy method for investigating chiral properties at the molecular level. ECD calculations with the commonly used linear-response time-dependent density functional theory (LR-TDDFT) framework can be prohibitively costly for large systems. To alleviate this problem, we present here an ECD implementation within the projector augmented-wave method in a real-time-propagation TDDFT framework in the open-source GPAW code. Our implementation supports both local atomic basis sets and real-space finite-difference representations of wave functions. We benchmark our implementation against an existin…

Chemical Physics (physics.chem-ph)Condensed Matter - Materials Sciencemagneettiset ominaisuudetCondensed Matter - Mesoscale and Nanoscale PhysicsspektroskopiatiheysfunktionaaliteoriaMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesorganometalliyhdisteetoptiset ominaisuudetPhysics - Chemical PhysicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)Physics::Atomic and Molecular Clustersnanohiukkaset
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Density-Functional Theory on Graphs

2021

The principles of density-functional theory are studied for finite lattice systems represented by graphs. Surprisingly, the fundamental Hohenberg–Kohn theorem is found void, in general, while many insights into the topological structure of the density-potential mapping can be won. We give precise conditions for a ground state to be uniquely v-representable and are able to prove that this property holds for almost all densities. A set of examples illustrates the theory and demonstrates the non-convexity of the pure-state constrained-search functional. peerReviewed

Chemical Physics (physics.chem-ph)Quantum PhysicstiheysfunktionaaliteoriaGeneral Physics and AstronomyFOS: Physical sciences02 engineering and technologyMathematical Physics (math-ph)021001 nanoscience & nanotechnology01 natural sciencesPhysics - Chemical Physics0103 physical scienceskvanttimekaniikkaPhysical and Theoretical Chemistry010306 general physics0210 nano-technologyQuantum Physics (quant-ph)Mathematical Physics
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Thiolate Adsorption on Au(hkl) and Equilibrium Shape of Large Thiolate-covered Gold Nanoparticles

2013

The adsorption of thiolates on Au surfaces employing density-functional-theory calculations has been studied. The dissociative chemisorption of dimethyl disulfide (CH3S−SCH3) on 14 different Au(hkl) is used as a model system. We discuss trends on adsorption energies, bond lengths, and bond angles as the surface structure changes, considering every possible Au(hkl) with h, k, l ≤ 3 plus the kinked Au(421). Methanethiolate (CH3S-) prefers adsorption on bridge sites on all surfaces considered; hollow and on top sites are highly unfavourable. The interface tensions for Au(hkl)-thiolate interfaces is determined at low coverage. Using the interface tensions in a Wulff construction method, we cons…

ChemistrytiheysfunktionaaliteoriaGeneral Physics and AstronomyNanoparticleDissociation (chemistry)kultaBond lengthCrystallographyMolecular geometryAdsorptionChemisorptionDensity functional theoryGoldPhysical and Theoretical ChemistryWulff constructionta116density functional theory
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Supramolecular Chirogenesis in Bis-Porphyrin: Crystallographic Structure and CD Spectra for a Complex with a Chiral Guanidine Derivative

2021

The complexation of (3aR,7aR)-N-(3,5-bis(trifluoromethyl)phenyl)octahydro-2H-benzo[d]imidazol-2-imine (BTI), as a guest, to ethane-bridged bis(zinc octaethylporphyrin), bis(ZnOEP), as a host, has been studied by means of ultraviolet-visible (UV-Vis) and circular dichroism (CD) absorption spectroscopies, single crystal X-ray diffraction, and computational simulation. The formation of 1:2 host-guest complex was established by X-ray diffraction and UV-Vis titration studies. Two guest BTI molecules are located at the opposite sides of two porphyrin subunits of bis(ZnOEP) host, which is resting in the anti-conformation. The complexation of BTI molecules proceed via coordination of the imine nitr…

Circular dichroismPhysics and Astronomy (miscellaneous)General MathematicsImineSupramolecular chemistrychiralityCrystal structurehost-guest binding010402 general chemistryguanidine01 natural sciencesDFTsupramolecular chemistrykemialliset sidoksetchemistry.chemical_compoundsupramolekulaarinen kemiaComputer Science (miscellaneous)Molecule[CHIM]Chemical SciencesGuanidine010405 organic chemistrylcsh:Mathematicstiheysfunktionaaliteoriahost–guest bindinglcsh:QA1-939Porphyrin0104 chemical sciencescircular dichroismCrystallographyTD-DFT simulationchemistryChemistry (miscellaneous)Chirality (chemistry)porphyrin
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Disorder and interactions in systems out of equilibrium : the exact independent-particle picture from density functional theory

2017

Density functional theory (DFT) exploits an independent-particle-system construction to replicate the densities and current of an interacting system. This construction is used here to access the exact effective potential and bias of non-equilibrium systems with disorder and interactions. Our results show that interactions smoothen the effective disorder landscape, but do not necessarily increase the current, due to the competition of disorder screening and effective bias. This puts forward DFT as a diagnostic tool to understand disorder screening in a wide class of interacting disordered systems.

Class (set theory)Current (mathematics)Non-equilibrium thermodynamicsFOS: Physical sciences02 engineering and technologyCondensed Matter::Disordered Systems and Neural Networks01 natural sciencesCondensed Matter - Strongly Correlated ElectronsInformationSystems_GENERALdisordered systems0103 physical sciencesMesoscale and Nanoscale Physics (cond-mat.mes-hall)strongly correlated systemsDisorder screeningStatistical physics010306 general physicsdensity functional theoryPhysicsta114Condensed Matter - Mesoscale and Nanoscale PhysicsStrongly Correlated Electrons (cond-mat.str-el)tiheysfunktionaaliteoriaDisordered Systems and Neural Networks (cond-mat.dis-nn)Condensed Matter - Disordered Systems and Neural Networks021001 nanoscience & nanotechnologynonequilibrium Green's functionParticleDensity functional theory0210 nano-technology
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Adiabatic versus non-adiabatic electron transfer at 2D electrode materials

2021

2D electrode materials are often deployed on conductive supports for electrochemistry and there is a great need to understand fundamental electrochemical processes in this electrode configuration. Here, an integrated experimental-theoretical approach is used to resolve the key electronic interactions in outer-sphere electron transfer (OS-ET), a cornerstone elementary electrochemical reaction, at graphene as-grown on a copper electrode. Using scanning electrochemical cell microscopy, and co-located structural microscopy, the classical hexaamineruthenium (III/II) couple shows the ET kinetics trend: monolayer > bilayer > multilayer graphene. This trend is rationalized quantitatively through th…

Computational chemistryMultidisciplinaryTKScienceQelektrodittiheysfunktionaaliteoriaGeneral Physics and Astronomy02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesGeneral Biochemistry Genetics and Molecular BiologyArticlesähkökemia0104 chemical sciencesCondensed Matter::Materials ScienceDensity functional theorygrafeeniQD0210 nano-technologyElectrocatalysisQC
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