Hyperfine Splitting In A Magnetic Field

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Homework Help Overview

The discussion revolves around the effect of a magnetic field on the hyperfine structure of Hydrogen in its ground state. Participants are tasked with computing the energy eigenvalues for different magnitudes of the magnetic field, specifically 1 gauss and 10,000 gauss, while considering the interactions of both the proton and electron magnetic moments.

Discussion Character

  • Exploratory, Conceptual clarification, Mathematical reasoning, Assumption checking

Approaches and Questions Raised

  • Participants explore the Hamiltonian related to the magnetic moments and question whether to apply it directly to the ground state wave function. There is discussion about treating the external magnetic field as a perturbation to the known hyperfine levels, with considerations on the validity of this approach based on the strength of the magnetic field.

Discussion Status

Some participants have provided references to external materials that may aid in understanding the topic. There is an ongoing exploration of the mathematical treatment of the problem, with various interpretations of how to incorporate the magnetic field into the Hamiltonian. No explicit consensus has been reached, but productive lines of inquiry are being pursued.

Contextual Notes

Participants note that the perturbation approach may only be valid for weaker magnetic fields compared to the hyperfine splitting, raising questions about the treatment of the interaction at higher field strengths.

jkrivda
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1. Problem:
Consider Hydrogen in its ground state in a magnetic field of magnitude B.
Compute the effect of the magnetic field on the hyperfine structure of Hydrogen
(that is you should include the interaction of both the proton and electron magnetic
moments with the applied magnetic field). Give the values of the energy eigenvalues
for B = 1 gauss and for B = 104 gauss.

Homework Equations


the hamiltonian for a dipole moment is H=-μB
μp=gpeSp/2mp
μe=-eSe/me
F=J+I where F is the atom's total angular momentum

The Attempt at a Solution


well, i think that the Hamiltonian looks like:
H=μeBp+Bext(μe+μp)
so do we just act this H on the ground state wave function?
 
Last edited:
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jkrivda said:
well, i think that the Hamiltonian looks like:
H=μeBp+Bext(μe+μp)
so do we just act this H on the ground state wave function?

Just a thought: From the wording of the problem, it seems to me that you want to find the effect of the external field on the hyperfine levels. So, I would think that you would assume the hyperfine levels are known and you just want to perturb those with the external field.

If so, wouldn't the perturbation part of the Hamiltonian just be due to the external field? Therefore you would have only the term Bext(μe+μp) as the perturbation? [EDIT: I think the term should have an overall negative sign.]

[EDIT 2: My comments might be invalid. You can only treat Bext(μe+μp) as a perturbation of the hyperfine levels if the perturbation is small compared to the hyperfine splitting. I think that might be true for an external field of 1 gauss, but not for 10,000 gauss. So, for 10,000 gauss I guess you have to treat both the hyperfine interaction and the external field interaction together as the perturbation of the unperturbed ground state level. Hope I'm not misleading you. Hopefully someone else will chime in.]
 
Last edited:
I think the name of topic is somewhat awkward.From what I understand,hyperfine splitting arises because of interaction of magnetic moment of proton with the spin of electron in hydrogen.By considering proton's magnetic moment arising from a localized current density one can write for the current associated with it as,
J=c(∇×M)
now this J gives rise to a potential,which can be calulatd from
A=k∫j(r')/|r-r'|(k is just some constant),now assuming a delta function source A gives
A=k'(∇×m)/r,{M=mδ(r')}
So B is given by B=∇×A,m is for proton which conventionally written as mp=(1/2)h-σpμp
now plugging it into m and evaluating B one writes for the interaction as
H'=-μe.B,(HERE μe is different from upper one)where B is just calculated
after it one uses some vector identity to get,
H'=-μeμp{(σ.σp)∇2-(σ.∇)(σp.∇)}(1/2r)(apart from some constant)
spherical averaging over s tate gives(because s state is spherically symmetric)
(σ.∇)(σp.∇)=1/3(σ.σp)∇2(be sure to verify it in spherical coordinates)
After which one gets,
H'=-μeμp(2/3)(σ.σp)∇2(1/2r)(apart from some constant)

this is evaluatd for ground state using the wavefunction of hydrogen(non-relativistic) to get
∫∇2(1/r)|ψ(r)|2 d3r=|ψ(0)|2(again some constant depending on unit chosen!)
After which (σ.σp)=-3 for singlet and 1 for triplet(easily seen by using S2=S12+S22+2S1.S2,IN TRIPLET S=1 and for singlet it is S=0)
the difference is taken for these two states for (σ.σp) will yield the required hyperfine splitting.
 
I just did not edit it,there are some mistakes.Like H' reads
H'=-μeσ.B,(I missed σ there):smile:
 

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