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Reduced density matrix functional theory (RDMFT) and coupled cluster theory restricted to paired double excitations (pCCD) are emerging as efficient methodologies for accounting for the so-called non-dynamic electronic correlation effects. Up to now, molecular calculations have been performed with real-valued orbitals. However, before extending the applicability of these methodologies to extended systems, where Bloch states are employed, the subtleties of working with complex-valued orbitals and the consequences of imposing time-reversal symmetry must be carefully addressed. In this work, we describe the theoretical and practical implications of adopting time-reversal symmetry in RDMFT and pCCD when allowing for complex-valued orbital coefficients. The theoretical considerations primarily affect the optimization algorithms, while the practical implications raise fundamental questions about the stability of solutions. Specifically, we find that complex solutions lower the energy when non-dynamic electronic correlation effects are pronounced. We present numerical examples to illustrate and discuss these instabilities and possible problems introduced by N-representability violations.
The Bethe-Salpeter equation has been extensively employed to compute the two-body electron-hole propagator and its poles which correspond to the neutral excitation energies of the system. Through a different time-ordering, the two-body Green's function can also describe the propagation of two electrons or two holes. The corresponding poles are the double ionization potentials and double electron affinities of the system. In this work, a Bethe-Salpeter equation for the two-body particle-particle propagator is derived within the linear-response formalism using a pairing field and anomalous propagators. This framework allows us to compute kernels corresponding to different self-energy approximations ($GW$, $T$-matrix, and second-Born) as in the usual electron-hole case. The performance of these various kernels is gauged for singlet and triplet valence double ionization potentials using a set of 23 small molecules. The description of double core hole states is also analyzed.
In a recent letter [Phys. Rev. Lett. 131, 216401] we presented the multichannel Dyson equation (MCDE) in which two or more many-body Green's functions are coupled. In this work we will give further details of the MCDE approach. In particular we will discuss: 1) the derivation of the MCDE and the definition of the space in which it is to be solved; 2) the rationale of the approximation to the multichannel self-energy; 3) a diagrammatic analysis of the MCDE; 4) the recasting of the MCDE on an eigenvalue problem with an effective Hamiltonian that can be solved using standard numerical techniques. This work mainly focuses on the coupling between the one-body Green's function and the three-body Green's function to describe photoemission spectra, but the MCDE method can be generalized to the coupling of other many-body Green's functions and to other spectroscopies.
Galvinoxyl, as one of the most extensively studied organic stable free radicals, exhibits a notable phase transition from a high-temperature (HT) phase with a ferromagnetic (FM) intermolecular interaction to a low-temperature (LT) phase with an antiferromagnetic (AFM) coupling at 85 K. Despite significant research efforts, the crystal structure of the AFM LT phase has remained elusive. This study successfully elucidates the crystal structure of the LT phase, which belongs to the P[1 with combining macron] space group. The crystal structure of the LT phase is found to consist of a distorted dimer, wherein the distortion arises from the formation of short intermolecular distances between anti-node carbons in the singly-occupied molecular orbital (SOMO). Starting from the structure of the LT phase, wave function calculations show that the AFM coupling 2J/kB varies significantly from −1069 K to −54 K due to a parallel shift of the molecular planes within the dimer.
Sujets
Xenon
Molecular descriptors
Perturbation theory
Diatomic molecules
Wave functions
Polarizabilities
Fonction de Green
QSAR
Atomic and molecular collisions
ALGORITHM
Atomic and molecular structure and dynamics
Anderson mechanism
Excited states
Molecular properties
Configuration Interaction
États excités
Dirac equation
X-ray spectroscopy
Electron electric dipole moment
3115vj
Quantum Monte Carlo
New physics
Parallel speedup
Path integral
Corrélation électronique
CP violation
Dipole
Abiotic degradation
3315Fm
AB-INITIO CALCULATION
Carbon Nanotubes
Green's function
Anharmonic oscillator
Approximation GW
Argile
Atom
3115vn
Ab initio calculation
Range separation
3470+e
Relativistic quantum mechanics
Auto-énergie
Large systems
Single-core optimization
Configuration interactions
Mécanique quantique relativiste
3115am
Atrazine-cations complexes
AB-INITIO
Atoms
Relativistic quantum chemistry
Dispersion coefficients
Quantum Chemistry
Coupled cluster calculations
Atomic data
Acrolein
Rydberg states
Adiabatic connection
Biodegradation
A posteriori Localization
Ion
3115ag
Atrazine
Valence bond
Density functional theory
Chimie quantique
BENZENE MOLECULE
Aimantation
Electron electric moment
Line formation
Hyperfine structure
A priori Localization
Atomic processes
Diffusion Monte Carlo
BIOMOLECULAR HOMOCHIRALITY
Atomic charges chemical concepts maximum probability domain population
3115bw
AROMATIC-MOLECULES
Argon
Analytic gradient
Pesticides Metabolites Clustering Molecular modeling Environmental fate Partial least squares
Numerical calculations
Electron correlation
CIPSI
Time-dependent density-functional theory
Coupled cluster
3115ae
Atomic charges
Ground states
Théorie des perturbations
Time reversal violation
Parity violation
Azide Anion
Petascale
Pesticide
Quantum chemistry
Spin-orbit interactions
Relativistic corrections
3115aj
Chemical concepts