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Bound He Rydberg states

The Hamiltonian for two spinless electrons at points r, and r2 relative to a He2+ core is given by3 [Pg.381]

To describe an atom with one electron in a Rydberg state a reasonable approach, termed Heisenberg s method by Bethe and Salpeter,3 is to separate the Hamiltonian of Eq (18.1) into two parts. Explicitly, [Pg.381]

For consistency with other bound Rydberg states we shall measure the energies relative to the ground state of He+. Expressed in this way, the energy of the state given in Eq. (18.5) is [Pg.382]

Following the Pauli exclusion principle we must antisymmetrize the wavefunctions when we include the spins of the two electrons. The wavefunction is given by a product of spatial and spin wave functions, i.e. [Pg.382]

Here 0+ is the spin wavefunction, and the + and - signs refer to the orthogonal singlet, 5 = 0 and triplet, 5=1 states, where 5 is the total electron spin. Using the wavefunctions of Eq. (18.7) we can calculate the first order corrections to Eq. (18.6) using the Hamiltonian of Eq. (18.2c). Explicitly, [Pg.382]


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