Shaoning Yao, Wei-Tsu Tseng, et al.
ADMETA 2011
Orbital functional theory (OFT) is based on a rule that determines a single-determinant reference state Φ for any exact N-electron eigenstate ψ. An OFT model postulates an explicit correlation energy functional Ec of occupied orbital functions {φi} and occupation numbers {ni}. The orbital Euler-Lagrange equations are analogous to Kohn-Sham equations, but do not in general contain local potential functions. Time-dependent Hartree-Fock theory is generalized in OFT to a formally exact linear response theory that includes electronic correlation. In the exchange-only limit, the theory reduces to the random-phase approximation of many-body theory. The formalism determines excitation energies. © 2002 John Wiley & Sons, Inc. Int. J. Quantum. Chem.
Shaoning Yao, Wei-Tsu Tseng, et al.
ADMETA 2011
Revanth Kodoru, Atanu Saha, et al.
arXiv
Surendra B. Anantharaman, Joachim Kohlbrecher, et al.
MRS Fall Meeting 2020
Michiel Sprik
Journal of Physics Condensed Matter