Search results for "nonequilibrium processes"

showing 4 items of 4 documents

Time propagation of the Kadanoff–Baym equations for inhomogeneous systems

2009

We have developed a time propagation scheme for the Kadanoff-Baym equations for general inhomogeneous systems. These equations describe the time evolution of the nonequilibrium Green function for interacting many-body systems in the presence of time-dependent external fields. The external fields are treated nonperturbatively whereas the many-body interactions are incorporated perturbatively using Phi-derivable self-energy approximations that guarantee the satisfaction of the macroscopic conservation laws of the system. These approximations are discussed in detail for the time-dependent Hartree-Fock, the second Born and the GW approximation.

DYNAMICSGW approximationPhysicsConservation lawNONEQUILIBRIUM PROCESSESCondensed Matter - Mesoscale and Nanoscale PhysicsStrongly Correlated Electrons (cond-mat.str-el)Time evolutionFOS: Physical sciencesGeneral Physics and AstronomyNon-equilibrium thermodynamicsELECTRON-GASSEMICONDUCTORSGREENS-FUNCTIONTRANSPORTATOMSCondensed Matter - Other Condensed MatterMOLECULESCondensed Matter - Strongly Correlated ElectronsClassical mechanicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)SCATTERINGPhysical and Theoretical ChemistryOther Condensed Matter (cond-mat.other)The Journal of Chemical Physics
researchProduct

Levels of self-consistency in the GW approximation

2009

We perform $GW$ calculations on atoms and diatomic molecules at different levels of self-consistency and investigate the effects of self-consistency on total energies, ionization potentials and on particle number conservation. We further propose a partially self-consistent $GW$ scheme in which we keep the correlation part of the self-energy fixed within the self-consistency cycle. This approximation is compared to the fully self-consistent $GW$ results and to the $G W_0$ and the $G_0W_0$ approximations. Total energies, ionization potentials and two-electron removal energies obtained with our partially self-consistent $GW$ approximation are in excellent agreement with fully self-consistent $…

GW approximationSelf consistencyGeneral Physics and AstronomyFOS: Physical sciencesELECTRON-GASGreen's function methodsATOMSMOLECULESQuality (physics)IonizationPhysics - Chemical Physicsionisation potentialWAVE-FUNCTIONSKOOPMANS THEOREMPhysical and Theoretical ChemistryfysiikkaPhysicsChemical Physics (physics.chem-ph)total energyNONEQUILIBRIUM PROCESSESDiatomic moleculeTRANSPORTCondensed Matter - Other Condensed MatterYield (chemistry)GROUND-STATECORRELATION ENERGIESIonization energyAtomic physicsEXTENSIONOther Condensed Matter (cond-mat.other)
researchProduct

Chemically Fueled Volume Phase Transition of Polyacid Microgels

2021

Abstract Microgels are soft colloids that show responsive behavior and are easy to functionalize for applications. They are considered key components for future smart colloidal material systems. However, so far microgel systems have almost exclusively been studied in classical responsive switching settings using external triggers, while internally organized, autonomous control mechanisms as found in supramolecular chemistry and DNA nanotechnology relying on fuel‐driven out‐of‐equilibrium concepts have not been implemented into microgel systems. Here, we introduce chemically fueled transient volume phase transitions (VPTs) for poly(methacrylic acid) (PMAA) microgels, where the collapsed hydr…

Phase transition540 Chemistry and allied sciencesMaterials scienceSupramolecular chemistry010402 general chemistrydissipative self-assembly01 natural sciencesnonequilibrium processesCatalysismicrogelschemistry.chemical_compoundColloidMicrogels | Hot PaperDNA nanotechnologyfuelsAutonomous controlResearch Articlespolymerschemistry.chemical_classification010405 organic chemistryMaterial systemGeneral ChemistryPolymerGeneral Medicine0104 chemical sciencesChemical engineeringMethacrylic acidchemistry540 ChemieResearch ArticleAngewandte Chemie
researchProduct

Multicomponent density-functional theory for time-dependent systems

2007

We derive the basic formalism of density functional theory for time-dependent electron-nuclear systems. The basic variables of this theory are the electron density in body-fixed frame coordinates and the diagonal of the nuclear N-body density matrix. The body-fixed frame transformation is carried out in order to achieve an electron density that reflects the internal symmetry of the system. We discuss the implications of this body-fixed frame transformation and establish a Runge-Gross-type theorem and derive Kohn-Sham equations for the electrons and nuclei. We illustrate the formalism by performing calculations on a one-dimensional diatomic molecule for which the many-body Schrodinger equati…

PhysicsDensity matrixElectron densityNONEQUILIBRIUM PROCESSESElectronic correlationDiagonalHartreeNUCLEARDiatomic moleculeFIELDSAtomic and Molecular Physics and OpticsSchrödinger equationPOLYATOMIC-MOLECULESMODELsymbols.namesakeClassical mechanicsLASER-PULSEQuantum mechanicsMOTIONSsymbolsSCHRODINGER-EQUATIONDensity functional theoryDOUBLE-IONIZATIONELECTRON CORRELATIONPhysical Review A
researchProduct