Heinz Schmid, Hans Biebuyck, et al.
Journal of Vacuum Science and Technology B: Microelectronics and Nanometer Structures
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.
Heinz Schmid, Hans Biebuyck, et al.
Journal of Vacuum Science and Technology B: Microelectronics and Nanometer Structures
E. Babich, J. Paraszczak, et al.
Microelectronic Engineering
P. Martensson, R.M. Feenstra
Journal of Vacuum Science and Technology A: Vacuum, Surfaces and Films
Elizabeth A. Sholler, Frederick M. Meyer, et al.
SPIE AeroSense 1997