Abstract
In order to calculate the average value of a physical quantity containing also many-particle interactions in a system of antisymmetric particles, a set of generalized density matrices are defined. In order to permit the investigation of the same physical situation in two complementary spaces, the Hermitean density matrix of order has two sets of indices of each variables, and it is further antisymmetric in each set of these indices.
Every normalizable antisymmetric wave function may be expanded in a series of determinants of order over all ordered configurations formed from a basic complete set of one-particle functions , which gives a representation of the wave function and its density matrices also in the discrete -space. The coefficients in an expansion of an eigenfunction to a particular operator may be determined by the variation principle, leading to the ordinary secular equation of the method of configurational interaction. It is shown that the first-order density matrix may be brought to diagonal form, which defines the "natural spin-orbitals" associated with the system. The situation is then partly characterized by the corresponding occupation numbers, which are shown to lie between 0 and 1 and to assume the value 1, only if the corresponding spin-orbital occurs in all configurations necessary for describing the situation. If the system has exactly spin-orbitals which are fully occupied, the total wave function may be reduced to a single Slater determinant. However, due to the mutual interaction between the particles, this limiting case is never physically realized, but the introduction of natural spin-orbitals leads then instead to a configurational expansion of most rapid convergence.
In case the basic set is of finite order , the best choice of this set is determined by a form of extended Hartree-Fock equations. It is shown that, in this case, the natural spin-orbitals approximately fulfill some equations previously proposed by Slater.
- Received 8 July 1954
DOI:https://doi.org/10.1103/PhysRev.97.1474
©1955 American Physical Society