We investigate the suitability of natural orbitals as a basis for describing many-body excitations. We analyze to which extent the natural orbitals describe both bound as well as ionized excited states and show that depending on the specifics of the excited state the ground-state natural orbitals may yield a good approximation. We show that the success of reduced density-matrix functional theory in describing molecular dissociation lies in the flexibility provided by fractional occupation numbers while the role of the natural orbitals is mino
Recently, an approximate theoretical framework was introduced, called local reduced density matrix f...
Author Institution: Department of Chemistry, Carnegle Institute of TechnologyThe wave function for a...
In recent years, several benchmark studies on the performance of large sets of functionals in time-d...
We investigate the suitability of natural orbitals as a basis for describing many-body excitations. ...
Pragmatic modeling of a chemical system requires a method that will produce results of desirable acc...
Straightforward interpretation of excitations is possible if they can be described as simple single ...
We investigate whether the natural orbitals (NOs) minimize ‖Ψ − Φ‖2, where Ψ is a wave function and ...
A combined strategy that unifies our interacting quantum atoms approach (IQA), a chemically intuitiv...
A natural orbital functional (NOF) satisfying the properties of the reduced density matrices is crit...
Using the equations of motion for the occupation numbers of natural spin orbitals we show that adiab...
The well-known natural orbitals are defined as eigenfunctions of a one-particle reduced density oper...
Any rigorous approach to first-order reduced density matrix (Γ) functional theory faces the phase di...
The shapes of molecular orbitals (MOs) in polyatomic molecules are often difficult for meaningful ch...
The non-vanishing of the natural orbital (NO) occupation numbers of the one-particle density matrix ...
Author Institution: Department of Chemistry, Iowa State CollegeSince expansions in terms of atomic o...
Recently, an approximate theoretical framework was introduced, called local reduced density matrix f...
Author Institution: Department of Chemistry, Carnegle Institute of TechnologyThe wave function for a...
In recent years, several benchmark studies on the performance of large sets of functionals in time-d...
We investigate the suitability of natural orbitals as a basis for describing many-body excitations. ...
Pragmatic modeling of a chemical system requires a method that will produce results of desirable acc...
Straightforward interpretation of excitations is possible if they can be described as simple single ...
We investigate whether the natural orbitals (NOs) minimize ‖Ψ − Φ‖2, where Ψ is a wave function and ...
A combined strategy that unifies our interacting quantum atoms approach (IQA), a chemically intuitiv...
A natural orbital functional (NOF) satisfying the properties of the reduced density matrices is crit...
Using the equations of motion for the occupation numbers of natural spin orbitals we show that adiab...
The well-known natural orbitals are defined as eigenfunctions of a one-particle reduced density oper...
Any rigorous approach to first-order reduced density matrix (Γ) functional theory faces the phase di...
The shapes of molecular orbitals (MOs) in polyatomic molecules are often difficult for meaningful ch...
The non-vanishing of the natural orbital (NO) occupation numbers of the one-particle density matrix ...
Author Institution: Department of Chemistry, Iowa State CollegeSince expansions in terms of atomic o...
Recently, an approximate theoretical framework was introduced, called local reduced density matrix f...
Author Institution: Department of Chemistry, Carnegle Institute of TechnologyThe wave function for a...
In recent years, several benchmark studies on the performance of large sets of functionals in time-d...