Why is the angular dependence of multielectron atom

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1. Describe the steps in a cycle of the self-consistent Hartree treatment of a multielectron atom. Why is the estimate of the net potential V(r) obtained at the end of a cycle more accurate than the estimate used at the beginning?

2. Why is the angular dependence of multielectron atom eigenfunctions the same as for oneelectron atom eigenfunctions? Why is the radial dependence different, except near the origin where it is the same?

Reference no: EM131352869

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