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Natural determinant reference functional theory
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DOI：10.1063/5.0180319.png)
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Abstract
En 中文
The natural determinant reference (NDR) or principal natural determinant is the Slater determinant comprised of the N most strongly occupied natural orbitals of an N-electron state of interest. Unlike the Kohn-Sham (KS) determinant, which yields the exact ground-state density, the NDR only yields the best idempotent approximation to the interacting one-particle reduced density matrix, but it is well-defined in common atom-centered basis sets and is representation-invariant. We show that the under-determination problem of prior attempts to define a ground-state energy functional of the NDR is overcome in a grand-canonical ensemble framework at the zero-temperature limit. The resulting grand potential functional of the NDR ensemble affords the variational determination of the ground state energy, its NDR (ensemble), and select ionization potentials and electron affinities. The NDR functional theory can be viewed as an exactification of orbital optimization and empirical generalized KS methods. NDR functionals depending on the noninteracting Hamiltonian do not require troublesome KS-inversion or optimized effective potentials.
Keywords:
1ST-ORDER DENSITY-MATRICES
EXCHANGE-CORRELATION HOLE
ELECTRON-DENSITIES
QUANTUM-THEORY
SPIN-ORBITALS
APPROXIMATIONS
CONVERGENCE
ENERGIES
Journal
IF:
3.1
Papers:
7.2W
Citations:
23.2W
