Search results for "Adiabatic process"

showing 10 items of 237 documents

Ground and excited state geometries via Mukherjee’s multireference coupled-cluster method

2012

Abstract A comprehensive study of molecular equilibrium structures is conducted to benchmark the multireference coupled-cluster (CC) method suggested by Mukherjee and coworkers (Mk-MRCC). We determine equilibrium structures and adiabatic excitation energies by applying the Mk-MRCC method within the singles and doubles (SD) approximation to ground and excited states of various small and medium-sized molecules. The results are compared to those obtained using other multireference or single-reference CC methods. For most molecules with a multireference ground state, it is found that equilibrium structures and excitation energies computed at the Mk-MRCCSD, equation-of-motion CCSD, multireferenc…

Coupled clusterChemistryExcited stateGeneral Physics and AstronomyMoleculePhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsGround stateAdiabatic processExcitationChemical Physics
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Three-state Landau-Zener model in the presence of dissipation

2019

A population transfer based on adiabatic evolutions in a three-state system undergoing an avoided crossing is considered. The efficiency of the process is analyzed in connection with the relevant parameters, bringing to light an important role of the phases of the coupling constants. The role of dissipation is also taken into account, focusing on external decays that can be described by effective non-Hermitian Hamiltonians. Though the population transfer turns out to be quite sensitive to the decay processes, for very large decay rates the occurrence of a Zeno-phenomenon allows for restoring a very high efficiency.

Coupling constantPhysicsQuantum PhysicsAvoided crossingFOS: Physical sciencesPopulation transferState (functional analysis)Dissipation01 natural sciencesSettore FIS/03 - Fisica Della Materia010305 fluids & plasmasConnection (mathematics)Landau-ZenerQuantum electrodynamicsadiabatic evolution0103 physical sciencesopen systemStandard linear solid modelQuantum Physics (quant-ph)010306 general physicsAdiabatic processPhysical Review A
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Quantum capture of charged particles by rapidly rotating symmetric top molecules with small dipole moments: analytical comparison of the fly-wheel an…

2013

The rate coefficients for capture of charged particles by spherical top molecules, which by isotopic substitution become symmetric top molecules with small dipole moment, are expressed analytically for the two limiting cases of weak coupling of the molecular angular momentum to the collision axis (dominating Coriolis interaction, the fly-wheel [FW] approximation) and strong coupling (negligible Coriolis interaction, the adiabatic channel [AC] approximation). The comparison leads to relations between rate coefficients for ultra-low (FW) and moderate (AC) temperatures and defines the range of parameters for which the analytical expressions become insufficient and a numerical treatment is nece…

CouplingPhysicsAngular momentumRange (particle radiation)BiophysicsCondensed Matter PhysicsCharged particleDipoleMoment (physics)Physical and Theoretical ChemistryAtomic physicsAdiabatic processMolecular BiologyQuantumMolecular Physics
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Quantum effects in the capture of charged particles by dipolar polarizable symmetric top molecules. II. Interplay between electrostatic and gyroscopi…

2013

ally nonadiabatic channel treatment of the capture of charged particles by dipolar polarizable symmetric top molecules with the aim to reveal quantum effects in the collision dynamics. In general, these effects are related to the discrete nature of the intrinsic, orbital, and total angular momenta, to the quantum character of passage of collision partners across effective potential barriers and drops, and to the interplay of two types of anisotropic interactions, the gyroscopic (Coriolis) and the electrostatic ones. The latter feature, in principle, leads to a coupling of capture channels. In the calculation of capture cross sections or rate coefficients, however, this coupling can be ignor…

CouplingSurface PropertiesChemistryStatic ElectricityIntermolecular forceGeneral Physics and AstronomyDeuteriumTritiumResonance (particle physics)Charged particleDipolePolarizabilityQuantum mechanicsQuantum TheoryParticle SizePhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsAdiabatic processMethaneQuantumHydrogenThe Journal of Chemical Physics
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Time-dependent alignment of molecules trapped in octahedral crystal fields.

2006

The hindered rotational states of molecules confined in crystal fields of octahedral symmetry, and their time-dependent alignment obtained by pulsed nonresonant laser fields, are studied computationally. The control over the molecular axis direction is discussed based on the evolution of the rotational wave packet generated in the cubic crystal-field potential. The alignment degree obtained in a cooperative case, where the alignment field is applied in a favorable crystal-field direction, or in a competitive direction, where the crystal field has a saddle point, is presented. The investigation is divided into two time regimes where the pulse duration is either ultrashort, leading to nonadia…

CrystalMolecular dynamicsField (physics)Radiation pressureOctahedral symmetryChemistrySaddle pointLibrationGeneral Physics and AstronomyPhysical and Theoretical ChemistryAtomic physicsAdiabatic processThe Journal of chemical physics
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Connection between optimal control theory and adiabatic-passage techniques in quantum systems

2012

This work explores the relationship between optimal control theory and adiabatic passage techniques in quantum systems. The study is based on a geometric analysis of the Hamiltonian dynamics constructed from the Pontryagin Maximum Principle. In a three-level quantum system, we show that the Stimulated Raman Adiabatic Passage technique can be associated to a peculiar Hamiltonian singularity. One deduces that the adiabatic pulse is solution of the optimal control problem only for a specific cost functional. This analysis is extended to the case of a four-level quantum system.

DYNAMICSN-LEVEL SYSTEMSStimulated Raman adiabatic passageFOS: Physical sciences01 natural sciencesPULSE SEQUENCES010305 fluids & plasmasOpen quantum systemDESIGNQuantum mechanicsPhysics - Chemical Physics0103 physical sciences010306 general physicsAdiabatic processPhysicsChemical Physics (physics.chem-ph)Quantum PhysicsALGORITHMSAdiabatic quantum computationAtomic and Molecular Physics and OpticsNMRClassical mechanicsGeometric phaseAdiabatic invariantPOPULATION TRANSFERQuantum algorithmSTIRAPQuantum Physics (quant-ph)Hamiltonian (control theory)
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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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Adiabatic Elimination and Sub-space Evolution of Open Quantum Systems

2020

Efficient descriptions of open quantum systems can be obtained by performing an adiabatic elimination of the fast degrees of freedom and formulating effective operators for the slow degrees of freedom in reduced dimensions. Here, we perform the construction of effective operators in frequency space, and using the final value theorem or alternatively the Keldysh theorem, we provide a correction for the trace of the density matrix which takes into account the non trace-preserving character of the evolution. We illustrate our results with two different systems, ones where the eliminated fast subspace is constituted by a continuous set of states and ones with discrete states. Furthermore, we sh…

Density matrixTrace (linear algebra)Atomic Physics (physics.atom-ph)PopulationDegrees of freedom (statistics)FOS: Physical sciences01 natural sciences010305 fluids & plasmasPhysics - Atomic Physics[PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph]Physics - Chemical Physics0103 physical sciencesMesoscale and Nanoscale Physics (cond-mat.mes-hall)Statistical physics010306 general physicsAdiabatic processeducationComputingMilieux_MISCELLANEOUSPhysicsChemical Physics (physics.chem-ph)education.field_of_studyQuantum PhysicsCondensed Matter - Mesoscale and Nanoscale PhysicsDetailed balanceFinal value theorem[SDU]Sciences of the Universe [physics]Quantum Physics (quant-ph)Subspace topology
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Oscillator Strengths of Electronic Excitations with Response Theory using Phase Including Natural Orbital Functionals

2013

The key characteristics of electronic excitations of many-electron systems, the excitation energies ωα and the oscillator strengths fα, can be obtained from linear response theory. In one-electron models and within the adiabatic approximation, the zeros of the inverse response matrix, which occur at the excitation energies, can be obtained from a simple diagonalization. Particular cases are the eigenvalue equations of time-dependent density functional theory (TDDFT), time-dependent density matrix functional theory, and the recently developed phase-including natural orbital (PINO) functional theory. In this paper, an expression for the oscillator strengths fα of the electronic excitations is…

Density matrixta114Chemistryexcitation energytiheysfunktionaaliteoriaGeneral Physics and AstronomyTime-dependent density functional theoryelektronitAdiabatic theoremMatrix (mathematics)Quantum mechanicsExcited stateDensity functional theoryeigenvalues and eigenfunctionsPhysical and Theoretical ChemistryAdiabatic processEigenvalues and eigenvectorsJournal of Chemical Physics
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Colossal barocaloric effects in the complex hydride Li$_{2}$B$_{12}$H$_{12}$

2021

Traditional refrigeration technologies based on compression cycles of greenhouse gases pose serious threats to the environment and cannot be downscaled to electronic device dimensions. Solid-state cooling exploits the thermal response of caloric materials to external fields and represents a promising alternative to current refrigeration methods. However, most of the caloric materials known to date present relatively small adiabatic temperature changes ($|\Delta T| \sim 1$ K) and/or limiting irreversibility issues resulting from significant phase-transition hysteresis. Here, we predict the existence of colossal barocaloric effects (isothermal entropy changes of $|\Delta S| \sim 100$ JK$^{-1}…

DiffusionFOS: Physical sciencesThermodynamics02 engineering and technology010402 general chemistry01 natural sciences7. Clean energyIsothermal processEntropy (classical thermodynamics)Phase (matter)Adiabatic processPhysicsCondensed Matter - Materials ScienceMultidisciplinary:Física [Àrees temàtiques de la UPC]HydrideMaterials Science (cond-mat.mtrl-sci)Ciència dels materials021001 nanoscience & nanotechnologyCondensed Matter PhysicsMatèria condensadaMaterials science0104 chemical sciences3. Good healthHysteresis13. Climate action0210 nano-technologyEnergy (signal processing)
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