Search results for "Charge Density"

showing 10 items of 206 documents

Oxide/water interfaces: how the surface chemistry modifies interfacial water properties

2012

The organization of water at the interface with silica and alumina oxides is analysed using density functional theory-based molecular dynamics simulation (DFT-MD). The interfacial hydrogen bonding is investigated in detail and related to the chemistry of the oxide surfaces by computing the surface charge density and acidity. We find that water molecules hydrogen-bonded to the surface have different orientations depending on the strength of the hydrogen bonds and use this observation to explain the features in the surface vibrational spectra measured by sum frequency generation spectroscopy. In particular, 'ice-like' and 'liquid-like' features in these spectra are interpreted as the result o…

ChemistryHydrogen bondInorganic chemistryOxideCharge densityCondensed Matter PhysicsSpectral lineMolecular dynamicschemistry.chemical_compoundChemical physicsMoleculeGeneral Materials ScienceDensity functional theoryPhysics::Chemical PhysicsSum frequency generation spectroscopyJournal of Physics: Condensed Matter
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Variation of the Fermi level and the electrostatic force of a metallic nanoparticle upon colliding with an electrode.

2017

When a metallic nanoparticle (NP) comes in close contact with an electrode, its Fermi level equilibrates with that of the electrode if their separation is less than the cut-off distance for electron tunnelling. In the absence of chemical reactions in solution, the charge on the metallic nanoparticle is constant outside this range before or after the collision. However, the double layer capacitances of both the electrode and the NP are influenced by each other, varying as the function of distance. Because the charge on the nanoparticle is constant, the outer potential of the metallic NP and hence its Fermi level varies as the capacitance changes. This effect is more pronounced for small part…

Ideally polarizable electrodeStandard hydrogen electrodeChemistryFermi levelCharge density02 engineering and technologyGeneral ChemistryElectron010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMolecular physicsHalf-cell0104 chemical sciencessymbols.namesakeChemistryElectrodesymbolsPoint of zero chargeAtomic physics0210 nano-technologyChemical science
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1H nmr chemical shifts of [14]annulenes and their dianion salts

1987

Abstract The bridged (14]annulene 2 was reduced into its dianion and the structure of the dianion salt was proven by chemical and spectroscopic means. The 1H NMR spectroscopic properties of 2 are similar to those of the structurally related bridged [14]annulene 1 , whereas the corresponding dianions 2 2- and 1 2- are strikingly different. The geometries of 1 and 2 and their dianions were studied by means of a modified π-SCF force field approach. Almost planar perimeters without significant bond length alternation are obtained for the neutral annulenes 1 and 2 , whereas their dianions are characterized by structures with reduced symmetry. The 1H chemical shifts of the bridged [14]annulenes a…

Electronic correlationChemistryStereochemistryChemical shiftOrganic ChemistryCharge densityNuclear magnetic resonance spectroscopyAnnuleneConjugated systemBiochemistryCrystallographyDrug DiscoveryProton NMRMoleculeTetrahedron
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Elastic, electronic and optical properties of boron- and nitrogen-doped 4,12,4-graphyne nanosheet

2020

Abstract The effects of boron (B) and nitrogen (N) dopants on 4,12,4-graphyne have been systematically investigated with density functional theory (DFT) calculations. The charge density analysis reveals that the N dopant at the sp-site destroys the acetylenic linkage in 4,12,4-graphyne, but instead tends to form a polar bond. The B- and N-doped 4,12,4-graphyne systems exhibit p- and n- semiconductor characters, respectively. Some obvious spin splitting polarizations can be observed in their band structures and DOS. Moreover, there is a giant difference in effective masses between electrons and electron holes, especially for B-doped 4,12,4-graphyne at C5 site. The directional electron and el…

Materials scienceDopantbusiness.industryCharge densitychemistry.chemical_element02 engineering and technologyElectron holeElectron010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesMolecular physicsAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsGraphyneSemiconductorchemistryDensity functional theory0210 nano-technologyBoronbusinessPhysica E: Low-dimensional Systems and Nanostructures
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Evolution of structural and electronic properties of TiSe2 under high pressure

2021

A pressure-induced structural phase transition and its intimate link with the superconducting transition was studied for the first time in TiSe2 up to 40 GPa at room temperature using X-ray diffraction, transport measurement, and first-principles calculations. We demonstrate the occurrence of a first-order structural phase transition at 4 GPa from the standard trigonal structure (S.G.P3¯m1) to another trigonal structure (S-G-P3¯c1). Additionally, at 16 GPa, the P3¯c1 phase spontaneously transforms into a monoclinic C2/m phase, and above 24 GPa, the C2/m phase returns to the initial P3¯m1 phase. Electrical transport results show that metallization occurs above 6 GPa. The charge density wave …

DiffractionSuperconductivityPhase transitionSuperconductivityMaterials scienceCondensed matter physics:Física [Àrees temàtiques de la UPC]Transition metalPhase (matter)General Materials SciencePhysical and Theoretical ChemistrySuperconductivitatCharge density waveMonoclinic crystal systemPhase diagram
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The weight function for charges - A rigorous theoretical concept for Kelvin probe force microscopy

2016

A comprehensive discussion of the physical origins of Kelvin probe force microscopy (KPFM) signals for charged systems is given. We extend the existing descriptions by including the openloop operation mode, which is relevant when performing KPFM in electrolyte solutions. We define the contribution of charges to the KPFM signal by a weight function, which depends on the electric potential and on the capacitance of the tip-sample system. We analyze the sign as well as the lateral decay of this weight function for different sample types, namely, conductive samples as well as dielectric samples with permittivities both larger and smaller than the permittivity of the surrounding medium. Dependin…

PermittivityKelvin probe force microscopeWeight functionta114Condensed matter physicsbusiness.industryChemistryGeneral Physics and AstronomyCharge density02 engineering and technologyDielectric021001 nanoscience & nanotechnologyKelvin probe force microscopy01 natural sciencesSignalCapacitance530Optics0103 physical sciencesElectric potential010306 general physics0210 nano-technologybusiness
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Tunable Interaction Strength and Nature of the S···Br Halogen Bonds in [(Thione)Br2] Systems

2015

The strength and nature of the S···Br and Br···Br interactions were systematically tuned by altering the electron donor properties of the thione group. Three new halogen-bonded compounds, [(N-methylbenzothiazole-2-thione)Br2]·0.5CH2Cl2 (1), [(2(3H)-benzothiazolethione)Br2] (2), and [(2-benzimidazolethione)Br]·[Br3] (3), were synthesized and studied structurally by using X-ray crystallography and computationally by using charge density analysis based on QTAIM calculations. Analysis of the interaction strength indicated a formation of surprisingly strong S···Br halogen bonds in 1 (−104 kJ mol–1, and RBrS = 0.64) and 2 (−116 kJ mol–1, and RBrS = 0.63) with a substantial covalent contribution. …

thionessynthesis010405 organic chemistryChemistryLigandStereochemistryCharge densityElectron donorGeneral ChemistryInteraction energy010402 general chemistryCondensed Matter Physics01 natural sciencesHeterolysis0104 chemical sciences3. Good healthCrystallographychemistry.chemical_compoundhalogen bondingCovalent bondHalogenMoleculeGeneral Materials Scienceta116bromideCrystal Growth & Design
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Relativistic corrections to the elastic electron scattering fromPb208

1976

In the present work we have calculated the differential cross sections for the elastic electron scattering from $sup 208$Pb using the charge distributions resulting from various corrections. The point proton and neutron mass distributions have been calculated from the spherical wave functions for $sup 208$Pb obtained by Kolb et al. The relativistic correction to the nuclear charge distribution coming from the electromagnetic structure of the nucleon has been accomplished by assuming a linear superposition of Gaussian shapes for the proton and the neutron charge form factor. Results of this calculation are quite similar to an earlier calculation by Bertozzi et al., who have used a different …

PhysicsNuclear and High Energy PhysicsProtonScatteringNuclear TheoryForm factor (quantum field theory)Charge densityNeutronNuclear cross sectionAtomic physicsNuclear ExperimentNucleonEffective nuclear chargePhysical Review C
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Molecular scale structure and dynamics at an ionic liquid/electrode interface.

2017

After a century of research, the potential-dependent ion distribution at electrode/electrolyte interfaces is still under debate. In particular for solvent-free electrolytes such as room-temperature ionic liquids, classical theories for the electrical double layer are not applicable. Using a combination of in situ high-energy X-ray reflectivity and impedance spectroscopy measurements, we determined this distribution with sub-molecular resolution. We find oscillatory charge density profiles consisting of alternating anion- and cation-enriched layers at both cathodic and anodic potentials. This structure is shown to arise from the same ion-ion correlations dominating the liquid bulk structure.…

ChemistryRelaxation (NMR)Analytical chemistryCharge density02 engineering and technologyElectrolyte010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesDielectric spectroscopyIonAnodechemistry.chemical_compoundChemical physicsIonic liquidElectrodePhysical and Theoretical Chemistry0210 nano-technologyFaraday discussions
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Valence Topological Charge-Transfer Indices for Dipole Moments

2003

Valence topological charge-transfer (CT) indices are applied to the calculation of dipole moments. The dipole moments calculated by algebraic and vector semisums of the CT indices are defined. The combination of the CT indices allows the estimation of the dipole moments. The model is generalized for molecules with heteroatoms. The ability of the indices for the description of the molecular charge distribution is established by comparing them with the dipole moment of the valence-isoelectronic series of benzene and styrene. Two CT indices, μ v e c (vector semisum of vertex-pair dipole moments) and μ V v e c (valence μ v e c ) are proposed. μ v e c and μ V v e c are important for the predicti…

Protein ConformationHeteroatomPharmaceutical ScienceBiochemistryAnalytical ChemistryElectricityComputational chemistryDrug DiscoveryPhysicsvalence topological charge-transfer indexChemistryCharge densityGeneral Medicinemolecular charge distributionCondensed Matter Physicstransdermal drug deliveryChemistry (miscellaneous)Molecular MedicineAtomic physicsInformation SystemsSteric effectsBond dipole momentStatic ElectricityTransition dipole momentBiophysicsElectronsFractal dimensionMolecular physicsBiophysical PhenomenaArticleCatalysislcsh:QD241-441Inorganic Chemistrylcsh:Organic chemistryAtomic orbitalMoleculePhysical and Theoretical ChemistryMolecular BiologyStyreneTopological quantum numberDipole momentModels StatisticalValence (chemistry)Chemical polarityOrganic ChemistryBenzeneModels Theoreticalvalence topological chargetransfer indexElectric dipole momentDipolephenyl alcoholModels ChemicalMoment (physics)Electric dipole transitionMolecules
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