Search results for "nanoscale"

showing 10 items of 752 documents

Lower Bounds on the Exchange-Correlation Energy in Reduced Dimensions

2009

Bounds on the exchange-correlation energy of many-electron systems are derived and tested. By using universal scaling properties of the electron-electron interaction, we obtain the exponent of the bounds in three, two, one, and quasi-one dimensions. From the properties of the electron gas in the dilute regime, the tightest estimate to date is given for the numerical prefactor of the bound, which is crucial in practical applications. Numerical tests on various low-dimensional systems are in line with the bounds obtained, and give evidence of an interesting dimensional crossover between two and one dimensions.

Chemical Physics (physics.chem-ph)Condensed Matter - Materials ScienceStrongly Correlated Electrons (cond-mat.str-el)Condensed Matter - Mesoscale and Nanoscale PhysicsCrossoverMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesGeneral Physics and AstronomyCondensed Matter - Strongly Correlated ElectronsQuantum dotPhysics - Chemical PhysicsQuantum mechanicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)Line (geometry)POÇOS QUÂNTICOSExponentDensity functional theoryStatistical physicsFermi gasScalingEnergy (signal processing)MathematicsPhysical Review Letters
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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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Design of high-temperature f-block molecular nanomagnets through the control of vibration-induced spin relaxation

2019

One of the main roadblocks that still hampers the practical use of molecular nanomagnets is their cryogenic working temperature. In the pursuit of rational strategies to design new molecular nanomagnets with increasing blocking temperature, ab initio methodologies play an important role by guiding synthetic efforts at the lab stage. Nevertheless, when evaluating vibration-induced spin relaxation, these methodologies are still far from being computationally fast enough to provide a useful predictive framework. Herein, we present an inexpensive first-principles method devoted to evaluating vibration-induced spin relaxation in molecular f-block single-ion magnets, with the important advantage …

Chemical Physics (physics.chem-ph)Condensed Matter - Mesoscale and Nanoscale PhysicsPhysics - Chemical PhysicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)FOS: Physical sciences
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Development of non-equilibrium Green's functions for use with full interaction in complex systems

2016

We present an ongoing development of an existing code for calculating groundstate, steady-state, and transient properties of many-particle systems. The development involves the addition of the full four-index two electron integrals, which allows for the calculation of transport systems, as well as the extension to multi-level electronic systems, such as atomic and molecular systems and other applications. The necessary derivations are shown, along with some preliminary results and a summary of future plans for the code. peerReviewed

Chemical Physics (physics.chem-ph)HistoryCondensed Matter - Mesoscale and Nanoscale PhysicsComputer scienceComplex systemFOS: Physical sciencesState (functional analysis)Extension (predicate logic)Molecular systemsComputer Science ApplicationsEducationDevelopment (topology)Physics - Chemical PhysicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)Code (cryptography)Transient (computer programming)Green's functionsStatistical physicscomplex systemsElectronic systems
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Theoretical study of new acceptor and donor molecules based on polycyclic aromatic hydrocarbons

2011

Functionalized polcyclic aromatic hydrocarbons (PAHs) are an interesting class of molecules in which the electronic state of the graphene-like hydrocarbon part is tuned by the functional group. Searching for new types of donor and acceptor molecules, a set of new PAHs has recently been investigated experimentally using ultraviolet photoelectron spectroscopy (UPS). In this work, the electronic structure of the PAHs is studied numerically with the help of B3LYP hybrid density functionals. Using the DELTA-SCF method, electron binding energies have been determined which affirm, specify and complement the UPS data. Symmetry properties of molecular orbitals are analyzed for a categorization and a…

Chemical Physics (physics.chem-ph)Materials scienceCondensed Matter - Mesoscale and Nanoscale PhysicsKoopmans' theoremFOS: Physical sciencesElectronic structureCharge-transfer complexAcceptorAtomic and Molecular Physics and OpticsCondensed Matter::Materials ScienceElectron affinity (data page)Chemical physicsPhysics - Chemical PhysicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)Molecular orbitalPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsHOMO/LUMOSpectroscopyBasis setJournal of Molecular Spectroscopy
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Salt-induced microheterogeneities in binary liquid mixtures

2017

The salt-induced microheterogeneity (MH) formation in binary liquid mixtures is studied by small-angle x-ray scattering (SAXS) and liquid state theory. Previous experiments have shown that this phenomenon occurs for antagonistic salts, whose cations and anions prefer different components of the solvent mixture. However, so far the precise mechanism leading to the characteristic length scale of MHs has remained unclear. Here, it is shown that MHs can be generated by the competition of short-ranged interactions and long-ranged monopole-dipole interactions. The experimental SAXS patterns can be reproduced quantitatively by fitting to the derived correlation functions without assuming any speci…

Chemical Physics (physics.chem-ph)Phase transitionSpinodalMaterials scienceCharacteristic lengthCondensed Matter - Mesoscale and Nanoscale PhysicsSmall-angle X-ray scatteringScatteringThermodynamicsFOS: Physical sciences02 engineering and technologyCondensed Matter - Soft Condensed Matter010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesSolventCondensed Matter::Soft Condensed MatterIonic strengthPhysics - Chemical PhysicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)Soft Condensed Matter (cond-mat.soft)0210 nano-technologyPhase diagram
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Nitrogen-Vacancy Magnetometry of Individual Fe-Triazole Spin Crossover Nanorods

2023

[Fe(Htrz)2(trz)](BF4) (Fe-triazole) spin crossover molecules show thermal, electrical, and optical switching between high spin (HS) and low spin (LS) states, making them promising candidates for molecular spintronics. The LS and HS transitions originate from the electronic configurations of Fe(II), and are considered to be diamagnetic and paramagnetic respectively. The Fe(II) LS state has six paired electrons in the ground states with no interaction with the magnetic field and a diamagnetic behavior is usually observed. While the bulk magnetic properties of Fe-triazole compounds are widely studied by standard magnetometry techniques their properties at the individual level are missing. Here…

Chemical Physics (physics.chem-ph)Quantum PhysicsCondensed Matter - Mesoscale and Nanoscale PhysicsPhysics - Chemical PhysicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)General EngineeringFOS: Physical sciencesGeneral Physics and AstronomyGeneral Materials ScienceQuantum Physics (quant-ph)ACS Nano
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Size-controlled magnetic nanoparticles in surfactant-rich thin films: a combined EXAFS, SAXS, AFM and MFM study

2008

Chemical synthesis methodAtomic force microscopyMagnetic NanoparticleStructure of nanoscale materials.Thin films morphologyTransmission electron microscopy
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Mesoscopic self-organisation of magnetic Cobalt-based nanofibers and nanoclusters in surfactant matrix

2008

Chemical synthesis methodThin film structure and morphologyAtomic force microscopy (AFM)Nanoscale materials and structures: fabrication and characterizationTransmission electron microscopy (TEM)Structure of nanoscale materials.
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Nonlinear chiral transport in Dirac semimetals

2018

We study the current of chiral charge density in a Dirac semimetal with two Dirac points in momentum space, subjected to an externally applied time dependent electric field and in the presence of a magnetic field. Based on the kinetic equation approach, we find contributions to the chiral charge current, that are proportional to the second power of the electric field and to the first and second powers of the magnetic field, describing the interplay of the chiral anomaly and the drift motion of electrons moving under the action of electric and magnetic fields.

Chiral anomalyPhysicsDirac semimetalsCondensed Matter - Mesoscale and Nanoscale Physicsta114chiral charge densityHigh Energy Physics::LatticeDirac (software)FOS: Physical sciencesCharge densityPosition and momentum space02 engineering and technologyElectron021001 nanoscience & nanotechnology01 natural sciencesAction (physics)Magnetic fieldQuantum electrodynamicsElectric fieldMesoscale and Nanoscale Physics (cond-mat.mes-hall)0103 physical sciences010306 general physics0210 nano-technologyPhysical Review B
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