Search results for "funktion"

showing 10 items of 213 documents

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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Magnetically induced currents and aromaticity in ligand-stabilized Au and AuPt superatoms

2021

Understanding magnetically induced currents (MICs) in aromatic or metallic nanostructures is crucial for interpreting local magnetic shielding and NMR data. Direct measurements of the induced currents have been successful only in a few planar molecules but their indirect effects are seen in NMR shifts of probe nuclei. Here, we have implemented a numerically efficient method to calculate gauge-including MICs in the formalism of auxiliary density functional theory. We analyze the currents in two experimentally synthesized gold-based, hydrogen-containing ligand-stabilized nanoclusters [HAu9(PPh3)8]2+ and [PtHAu8(PPh3)8]+. Both clusters have a similar octet configuration of Au(6s)-derived deloc…

Computational chemistrySciencetiheysfunktionaaliteoriaMethod developmentQPhysics::Opticssähkövirtalaskennallinen kemiaequipment and suppliescomputational chemistryArticleNanoparticlesnanoparticlesnanohiukkasetmethod developmenthuman activitiesNature Communications
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Density functional theory description of random Cu-Au alloys

2019

Density functional alloy theory is used to accurately describe the three core effects controlling the thermodynamics of random Cu-Au alloys. These three core effects are exchange correlation (XC), local lattice relaxations (LLRs), and short-range order (SRO). Within the real-space grid-based projector augmented-wave (GPAW) method based on density functional theory (DFT), we adopt the quasinonuniform XC approximation (QNA), and take into account the LLR and the SRO effects. Our approach allows us to study the importance of all three core effects in a unified way within one DFT code. The results demonstrate the importance of the LLR term and show that going from the classical gradient level a…

Copper alloysfirst-principles calculationstiheysfunktionaaliteoriaDensity functional theoryThermodynamicsmetalliseoksetBinary alloyselectronic structureGold alloysLunar surface analysis
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Solvent directs the dimensionality of Cu-dicyanoimidazoles

2022

In this paper, we report one-pot reactions of the same reactants 4,5-dicyanoimidazole and CuI in different solvents. In pure MeCN, the reaction resulted in previously reported MOF structure [Cu(4,5-dicyanoimidazole)]n.(MeCN)0.5n (1). On the other hand, when MeCN/MeOH solvent mixture was used, a new coordination polymer [Cu(4,5-dicyanoimidazole)(MeCN)(CuI)]n (2) was formed. The crystallization yielded very different structures as determined by X-ray crystallography. In 1, the solvent molecule acetonitrile occupies the MOF pores via weak interactions, but in 2 it is coordinated to the metal center. Computational DFT calculations and topological charge density analysis were utilized to explore…

Copper complextiheysfunktionaaliteoriakupariGeneral ChemistrykompleksiyhdisteetSolvent effectCondensed Matter PhysicsDFTQTAIMCyanoGeneral Materials ScienceImidazolekristallisaatioliuottimet
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Designing Dissensual Common Sense: Critical Art, Architecture, and Design in Jacques Rancière’s Political Thought

2021

How can design be socially engaged and politically efficient, as proposed by discourses labeled as critical design? This article introduces a conceptualization and historiography of politically charged design discourse based on philosopher Jacques Rancière’s work on the intersections of politics, aesthetics, and critical artistic practices. By focusing especially on Rancière’s reading of the genealogy of design from Ruskin to constructivism and the Bauhaus, the article aims to show that there is an important connection between design and politics present in Rancière’s thought. Rather than solely revealing the oppressive dimension embedded in designed forms, for Rancière, design is itself a …

Cultural StudiesVisual Arts and Performing Artsmedia_common.quotation_subjectfunktionalismipolitiikan teoriaRancière JacquesPoliticsPolitical philosophySociologyCritical designArchitecturemedia_commonpolitical designConceptualizationHistoriographyCommon sensecritical designarkkitehtuuriJacques RancièreestetiikkaEpistemologymuotoilukonstruktivismi (taide)poliittisuuskriittinen teoriaArts and Crafts -liikeDesign and Culture
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Dipolar coupling of nanoparticle-molecule assemblies: An efficient approach for studying strong coupling

2021

Strong light-matter interactions facilitate not only emerging applications in quantum and non-linear optics but also modifications of materials properties. In particular the latter possibility has spurred the development of advanced theoretical techniques that can accurately capture both quantum optical and quantum chemical degrees of freedom. These methods are, however, computationally very demanding, which limits their application range. Here, we demonstrate that the optical spectra of nanoparticle-molecule assemblies, including strong coupling effects, can be predicted with good accuracy using a subsystem approach, in which the response functions of the different units are coupled only a…

Degrees of freedom (statistics)General Physics and AstronomyNanoparticleFOS: Physical sciences010402 general chemistryoptiset ominaisuudet01 natural scienceslinear combination of atomic orbitalstime dependent density functional theorynanorakenteet0103 physical sciencesMesoscale and Nanoscale Physics (cond-mat.mes-hall)MoleculePhysical and Theoretical Chemistryoptical spectroscopyQuantumPhysicssurface optics010304 chemical physicsCondensed Matter - Mesoscale and Nanoscale Physicstiheysfunktionaaliteoriapolarizability0104 chemical sciencesplasmonitRange (mathematics)DipoleChemical physicsDensity functional theorynanoparticlesnanohiukkasetplasmonsMagnetic dipole–dipole interaction
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Response calculations based on an independent particle system with the exact one-particle density matrix: Excitation energies

2012

Adiabatic response time-dependent density functional theory (TDDFT) suffers from the restriction to basically an occupied → virtual single excitation formulation. Adiabatic time-dependent density matrix functional theory allows to break away from this restriction. Problematic excitations for TDDFT, viz. bonding-antibonding, double, charge transfer, and higher excitations, are calculated along the bond-dissociation coordinate of the prototype molecules H2 and HeH+ using the recently developed adiabatic linear response phase-including (PI) natural orbital theory (PINO). The possibility to systematically increase the scope of the calculation from excitations out of (strongly) occupied into wea…

Density matrix/dk/atira/pure/sustainabledevelopmentgoals/affordable_and_clean_energyChemistrytiheysfunktionaaliteoriaGeneral Physics and AstronomyTime-dependent density functional theoryAtomic orbitalExcited stateDensity functional theorySDG 7 - Affordable and Clean EnergyPhysical and Theoretical ChemistryAtomic physicsPhysics::Chemical PhysicsAdiabatic processHOMO/LUMOExcitationdensity functional theoryJournal of Chemical Physics
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