So adding this to the (easier) part above, we have
E(1)n =
eB
2 mc(
mj ̄h±
mj ̄h
2 ℓ+ 1)
=
e ̄hB
2 mcmj(
1 ±
1
2 ℓ+ 1
)
forj=ℓ±^12.
In summary then, we rewrite the fine structure shift.
∆E=−
1
2
mc^2 (Zα)^41
n^3[
1
j+^12−
3
4 n]
To this we add the anomalous Zeeman effect
∆E=
e ̄hB
2 mcmj(
1 ±
1
2 ℓ+ 1
)
23.5 Homework Problems
- Consider the fine structure of then= 2 states of the hydrogen atom. What is the spectrum
 in the absence of a magnetic field? How is the spectrum changed whenthe atom is placed in a
 magnetic field of 25,000 gauss? Give numerical values for the energyshifts in each of the above
 cases. Now, try to estimate the binding energy for the lowest energyn= 2 state including the
 relativistic, spin-orbit, and magnetic field.
- Verify the relations used for^1 r,r^12 , andr^13 for hydrogen atom states up ton= 3 and for any
 nifl=n−1.
- Calculate the fine structure of hydrogen atoms for spin 1 electrons forn= 1 andn= 2.
 Compute the energy shifts in eV.
23.6 Sample Test Problems
- The relativistic correction to the Hydrogen Hamiltonian is H 1 = − p
4
8 m^3 c^2. Assume that
electrons have spin zero and that there is therefore no spin orbit correction. Calculate the
energy shifts and draw an energy diagram for the n=3 states of Hydrogen. You may use〈ψnlm|^1 r|ψnlm〉=n (^21) a 0 and〈ψnlm|r^12 |ψnlm〉=n (^3) a 21
0 (l+^12 )
.
- Calculate the fine structure energy shifts (in eV!) for then= 1,n= 2, andn= 3 states
 of Hydrogen. Include the effects of relativistic corrections, the spin-orbit interaction, and the
 so-called Darwin term (due to Dirac equation). Do not include hyperfine splitting or the effects
 of an external magnetic field. (Note: I am not asking you to derive the equations.) Clearly list
 the states in spectroscopic notation and make a diagram showing the allowed electric dipole
 decays of these states.
- Calculate and show the splitting of then= 3 states (as in the previous problem) in a weak
 magnetic field B. Draw a diagram showing the states before and after the field is applied
- If the general form of the spin-orbit coupling for a particle of massmand spinS~moving in a
 potentialV(r) isHSO= 2 m^12 c 2 L~·S~^1 rdVdr, what is the effect of that coupling on the spectrum of
