Search results for "Charge density"

showing 10 items of 206 documents

Chiral charge order in the superconductor 2H-TaS(2)

2011

Artículo escrito por un elevado número de autores, solo se referencian el que aparece en primer lugar, el nombre del grupo de colaboración, si le hubiere, y los autores pertenecientes a la UAM

General Physics and AstronomyFOS: Physical sciences01 natural sciences010305 fluids & plasmaslaw.inventionSuperconductivity (cond-mat.supr-con)Condensed Matter - Strongly Correlated ElectronslawCondensed Matter::Superconductivity0103 physical sciences010306 general physicsSpectroscopyQuantum tunnellingComputingMilieux_MISCELLANEOUSPhysicsSuperconductivityCondensed matter physicsStrongly Correlated Electrons (cond-mat.str-el)Condensed Matter - SuperconductivityOrder (ring theory)FísicaCharge (physics)[PHYS.COND.CM-S]Physics [physics]/Condensed Matter [cond-mat]/Superconductivity [cond-mat.supr-con]Density of states[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]Scanning tunneling microscopeCharge density wave
researchProduct

Calcium binding and ionic conduction in single conical nanopores with polyacid chains: model and experiments.

2012

Calcium binding to fixed charge groups confined over nanoscale regions is relevant to ion equilibrium and transport in the ionic channels of the cell membranes and artificial nanopores. We present an experimental and theoretical description of the dissociation equilibrium and transport in a single conical nanopore functionalized with pH-sensitive carboxylic acid groups and phosphonic acid chains. Different phenomena are simultaneously present in this basic problem of physical and biophysical chemistry: (i) the divalent nature of the phosphonic acid groups fixed to the pore walls and the influence of the pH and calcium on the reversible dissociation equilibrium of these groups; (ii) the asym…

General Physics and AstronomyIonic bondingFunctionalizedDissociation (chemistry)Conical nanoporeNanoscale regionschemistry.chemical_compoundNanoporesI - V curveIonic conductivityGeneral Materials ScienceConical nanoporesPhosphonate groupCalcium concentrationChemistryGeneral EngineeringPH effectsPartition functionsIonic channelsIon equilibriumReversible dissociationChemical physicsFunctional groupsThermodynamicsDesalination membranesIon bindingPorosityDissociationBiophysical chemistryDissociation equilibriaInorganic chemistrychemistry.chemical_elementWater filtrationCalciumIonNernst-Planck equationsApplied potentialsIon bindingCarboxylationPhosphonic acidsComputer SimulationCarboxylateParticle SizeControlled drug releaseCurrent voltage curveIonsBinding SitesFixed charge densityPH sensitiveCarboxylic acidsDesalinationPhosphonic acid groupsPoly acidsElectric ConductivityCarboxylic acid groupsFixed ChargesNanostructuresCell membranesCurrent-voltage curvesModels ChemicalQuantum theoryFISICA APLICADACalciumBiological ion channelsCalcium bindingIonic currentCytologyPore wallStatistical mechanicsAcidsACS nano
researchProduct

Arsenite adsorption on goethite at elevated temperatures

2009

Abstract Experimental closed-system ΔT acid–base titrations between 10 °C and 75 °C were used to constrain a temperature-dependent 1-pK basic Stern model of the goethite surface complexation reactions. Experimental data for the temperature dependence of pHPZC determined by the one-term Van’t Hoff extrapolation yield a value for goethite surface protonation enthalpy of −49.6 kJ mol−1 in good agreement with literature data. Batch titration data between 10 °C and 75 °C with arsenite concentrations between 10 μM and 100 μM yield adsorption curves, which increases with pH, peak at a pH of 9, and decrease at higher pH values. The slope of this bend becomes steeper with increasing temperature. A 1…

GoethiteChemistryEnthalpyAnalytical chemistryMineralogyCharge densityPollutionchemistry.chemical_compoundAdsorptionGeochemistry and Petrologyvisual_artYield (chemistry)visual_art.visual_art_mediumEnvironmental ChemistryTitrationEquilibrium constantArseniteApplied Geochemistry
researchProduct

Effect of pH on the mobility of the herbicide MCPA in a sand-goethite column: 1D and 2D reactive transport modeling

2018

Abstract Adsorption and transport of the herbicide 2-methyl-4-chlorophenoxyacetic acid (MCPA) in a homogeneous sand-goethite system were investigated as a function of pH. Interaction of MCPA with the solid surface was geochemically modeled according to the charge distribution multisite complexation (CD-MUSIC) approach. Based on this calibration, retardation of MCPA transport in column experiments was significantly underestimated by conventional 1D simulations. As a new approach, Positron Emission Tomography (PET) was employed to analyze the flow field, using 18F− as a radiotracer. The observed heterogeneity was reproduced in 2D simulations assuming increased permeability and porosity at the…

GoethiteFlow (psychology)ThermodynamicsCharge density010501 environmental sciences010502 geochemistry & geophysics01 natural sciencesPollutionMCPAPermeability (earth sciences)chemistry.chemical_compoundAdsorptionchemistryGeochemistry and Petrologyvisual_artvisual_art.visual_art_mediumFluid dynamicsEnvironmental ChemistryPorosity0105 earth and related environmental sciencesApplied Geochemistry
researchProduct

Silicate adsorption by goethite at elevated temperatures

2009

Abstract Batch adsorption experiments with relatively low silica concentrations between 10 µM and 100 µM were conducted at three different ionic strength (0.01  − 0.1 M), and four different temperatures between 10 °C and 75 °C, yielding in a total of 550 experimental data points. The residual concentration of monosilicic acid is controlled by an adsorption equilibrium which is dependent on pH. The % Si adsorbed vs. − log[H + ] curves reveal an upward bend with a maximum at about a pH of 9. With acidification below pH 9 the residual Si concentration in the suspensions steadily increases, as well as in the increasingly alkaline pH range. The slope of the latter is becoming steeper with increa…

GoethiteInorganic chemistryEnthalpyAnalytical chemistryIonic bondingCharge densityGeologySilicatechemistry.chemical_compoundAdsorptionchemistryGeochemistry and PetrologyIonic strengthvisual_artvisual_art.visual_art_mediumSurface chargeChemical Geology
researchProduct

Fine-tuning halogen bonding properties of diiodine through halogen–halogen charge transfer – extended [Ru(2,2′-bipyridine)(CO)2X2]·I2 systems (X = Cl…

2016

The current paper introduces the use of carbonyl containing ruthenium complexes, [Ru(bpy)(CO)2X2] (X = Cl, Br, I), as halogen bond acceptors for a I2 halogen bond donor. In all structures, the metal coordinated halogenido ligand acts as the actual halogen bond acceptor. Diiodine, I2, molecules are connected to the metal complexes through both ends of the molecule forming bridges between the complexes. Due to the charge transfer from Ru–X to I2, formation of the first Ru–X⋯I2 contact tends to generate a negative charge on I2 and redistribute the electron density anisotropically. If the initial Ru–X⋯IA–IB interaction causes a notable change in the electron density of I2, the increased negativ…

Halogen bond010405 organic chemistryChemistryLigandchemistry.chemical_elementCharge densityGeneral Chemistry010402 general chemistryCondensed Matter PhysicsPhotochemistry01 natural sciencesAcceptor22'-Bipyridine0104 chemical sciencesRutheniumCrystallographychemistry.chemical_compoundhalogen bondingHalogenruthenium complexesMoleculeGeneral Materials Scienceta116CrystEngComm
researchProduct

Halogen bonds with coordinative nature: halogen bonding in a S–I+–S iodonium complex†

2015

A detailed study of unexpectedly strong iodonium–sulfur halogen bonds in [I(2-imidazolidinethione)2]+ is presented. The interactions are characterized by single-crystal X-ray diffraction, charge density analysis based on QTAIM calculations, mass spectrometry, and NMR spectroscopy. The results, small RIS = 0.7 and high interaction energy of −60 kJ mol−1, support a coordinative nature of the halogen bond between the iodonium ion and the sp2 hybridized sulfur atoms.

Halogen bondChemistryInorganic chemistryhalogen bondschemistry.chemical_elementCharge densityGeneral ChemistryNuclear magnetic resonance spectroscopyInteraction energyCondensed Matter PhysicsMass spectrometrySulfurIonCrystallographyHalogenGeneral Materials Scienceta116CrystEngComm
researchProduct

Concerted halogen and hydrogen bonding in [RuI2(H2dcbpy)(CO)2]···I2···(CH3OH)···I2···[RuI2(H2dcbpy)(CO)2].

2011

A new type of concerted halogen bond-hydrogen bond interaction was found in the solid state structure of [RuI(2)(H(2)dcbpy)(CO)(2)]···I(2)···(MeOH)···I(2)···[RuI(2)(H(2)dcbpy)(CO)(2)]. The iodine atoms of the two I(2) molecules interact simultaneously with each other and with the OH group of methanol of crystallization. The interaction was characterized by single crystal X-ray measurements and by computational charge density analysis based on DFT calculations.

Hydrogen bondMetals and AlloysCharge densityGeneral ChemistrySolid state structureCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionchemistry.chemical_compoundCrystallographychemistryComputational chemistrylawHalogenMaterials ChemistryCeramics and CompositesMoleculeMethanolCrystallizationSingle crystalta116Chemical communications (Cambridge, England)
researchProduct

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
researchProduct

Rational Design of Single-Ion Magnets and Spin Qubits Based on Mononuclear Lanthanoid Complexes

2012

Here we develop a general approach to calculating the energy spectrum and the wave functions of the low-lying magnetic levels of a lanthanoid ion submitted to the crystal field created by the surrounding ligands. This model allows us to propose general criteria for the rational design of new mononuclear lanthanoid complexes behaving as single-molecule magnets (SMMs) or acting as robust spin qubits. Three typical environments exhibited by these metal complexes are considered, namely, (a) square antiprism, (b) triangular dodecahedron, and (c) trigonal prism. The developed model is used to explain the properties of some representative examples showing these geometries. Key questions in this ar…

Inorganic ChemistryLanthanideDelocalized electronDodecahedronAb initio quantum chemistry methodsChemistryComputational chemistryCharge densityPhysical and Theoretical ChemistrySpin (physics)Molecular physicsSquare antiprismIonInorganic Chemistry
researchProduct