In atomic physics, the Landé interval rule [1] states that, due to weak angular momentum coupling (either spin-orbit or spin-spin coupling), the energy splitting between successive sub-levels are proportional to the total angular momentum quantum number (J or F) of the sub-level with the larger of their total angular momentum value (J or F). [2][3]

Background

The rule assumes the Russell–Saunders coupling and that interactions between spin magnetic moments can be ignored. The latter is an incorrect assumption for light atoms. As a result of this, the rule is optimally followed by atoms with medium atomic numbers.[4]

The rule was first stated in 1923 by German-American physicist Alfred Landé.[1]

Derivation

As an example,[2] consider an atom with two valence electrons and their fine structures in the LS-coupling scheme. We will derive heuristically the interval rule for the LS-coupling scheme and will remark on the similarity that leads to the interval rule for the hyperfine structure.

The interactions between electrons couple their orbital and spin angular momentums. Let's denote the spin and orbital angular momentum as and for each electrons. Thus, the total orbital angular momentum is and total spin momentum is . Then the coupling in the LS-scheme gives rise to a Hamiltonian:

where and encode the strength of the coupling. The Hamiltonian acts as a perturbation to the state . The coupling would cause the total orbital and spin angular momentums to change directions, but the total angular momentum would remain constant. Its z-component would also remain constant, since there is no external torque acting on the system. Therefore, we shall change the state to , which is a linear combination of various . The exact linear combination, however, is unnecessary to determine the energy shift.

To study this perturbation, we consider the vector model where we treat each as a vector. and precesses around the total orbital angular momentum . Consequently, the component perpendicular to averages to zero over time, and thus only the component along needs to be considered. That is, . We replace by and by the expectation value .

Applying this change to all the terms in the Hamiltonian, we can rewrite it as

The energy shift is then

Now we can apply the substitution to write the energy as

Consequently, the energy interval between adjacent sub-levels is:

This is the Landé interval rule.

As an example, consider a term, which has 3 sub-levels . The separation between and is , twice as the separation between and is .

As for the spin-spin interaction responsible for the hyperfine structure, because the Hamiltonian of the hyperfine interaction can be written as

where is the nuclear spin and is the total angular momentum, we also have an interval rule:

where is the total angular momentum . The derivation is essentially the same, but with nuclear spin , angular momentum and total angular momentum .

Limitations

The interval rule holds when the coupling is weak. In the LS-coupling scheme, a weak coupling means the energy of spin-orbit coupling is smaller than residual electrostatic interaction: . Here the residual electrostatic interaction refers to the term including electron-electron interaction after we employ the central field approximation to the Hamiltonian of the atom. For the hyperfine structure, the interval rule for two magnetic moments can be disrupted by magnetic quadruple interaction between them, so we want . [2]

For example, in helium, the spin-spin interactions and spin-other-orbit interaction have an energy comparable to that of the spin-orbit interaction. [2]

References

  1. 1 2 Landé, A. Termstruktur und Zeemaneffekt der Multipletts. Z. Physik 15, 189–205 (1923). https://doi.org/10.1007/BF01330473
  2. 1 2 3 4 Foot, Christopher J (2005). Atomic Physics (1st ed.). ISBN 978-0-19-850695-9. Retrieved December 11, 2020.
  3. Morris, Christopher G. (1992). Academic Press dictionary of science and technology. Academic Press. pp. 1201. ISBN 0-12-200400-0.
  4. E. U. Condon and G. H. Shortley, The Theory of Atomic Spectra, Cambridge University Press, 1959, p 193.
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