Calculating Expectation Value of Angular Momentum Squared for Hydrogen Atom

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Homework Help Overview

The discussion revolves around calculating the expectation value of angular momentum squared for a hydrogen atom, given a specific superposition of normalized energy eigenfunctions. The subject area includes quantum mechanics and angular momentum operators.

Discussion Character

  • Exploratory, Conceptual clarification, Mathematical reasoning

Approaches and Questions Raised

  • Participants explore the relationship between the coefficients of the wave function and the expectation value of angular momentum squared. There is discussion about whether an integral is necessary for the calculation and how to incorporate the L2 operator into the expectation value.

Discussion Status

Some participants have provided guidance on the expectation value formulation and the use of coefficients. There is an ongoing exploration of the implications of using the L2 operator and how it relates to the eigenstates of the system. Multiple interpretations of the approach are being discussed.

Contextual Notes

Participants are navigating the complexities of quantum mechanics, particularly in relation to angular momentum and the properties of eigenstates. There is mention of specific quantum numbers associated with the eigenfunctions, which may influence the calculations.

sian130
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Homework Statement



Consider a hydrogen atom whose wave function at time t=0 is the following superposition of normalised energy eigenfunctions:

Ψ(r,t=0)=1/3 [2ϕ100(r) -2ϕ321(r) -ϕ430(r) ]

What is the expectation value of the angular momentum squared?

Homework Equations



I know that L2 operator is:

-ℏ2 [1/sinθ d/dθ sinθ d/dθ+1/(sin2 θ) d2/dϕ2 ]

although I don't think I need to use it.

I know L2=Lx2+Ly2+Lz2

The Attempt at a Solution



I am confused as to how to go about this. I don't think I need to be calculating an integral, as you would do to find the expectation value of, for example, x2 for a wavefunction. I think I need to calculate the number from squaring the coefficients of each part, and adding, but I'm not sure how to incorporate the L2 bit into this?

I would appreciate any help, I have been puzzling over this for ages now!
 
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Hopefully you remember that the expectation value of L^2 in a state \vert\psi\rangle is
\langle\psi\vert L^2\vert\psi\rangle
When you plug in the given wavefunction, what do you get?

Now, what is the expectation value of L^2 in an eigenstate \vert\psi_{nlm}\rangle, in terms of the quantum numbers n,l,m?
 
Ok I know that:

〈H ̂ 〉= <S|H ̂|S>

which is:

=sum(a*nam<En|H|Em>)
=sum(a*nam<En|Em|Em>)
=sum(a*namEm<En|Em>)
=sum(a*namEmdeltamn)
=sum(|am|2 En)
=<E>

So am I right in thinking that I just have to do:

<L2> = sum(|coefficients|2 * L2)

If so, what do I use for L2?

Is it l(l+1)hbar2 ?

Thanks
 
Sounds like you're on the right track.
 
Thank you for getting back to me so quickly.

I did as above, and got:

1/3(22l(l+1)hbar2 + 22l(l+1)hbar2 + l(l+1)hbar2)

Then used the values of l given in the subscript of each eigenfunction, and got an overall answer of 12hbar2. Does that sound about right?

Thanks again x
 
sian130 said:
1/3(22l(l+1)hbar2 + 22l(l+1)hbar2 + l(l+1)hbar2)
At the beginning, remember that you get a factor of 1/3 from each \psi in
\langle\psi\vert L^2 \vert\psi\rangle
Other than that, it seems OK.
 
May I ask why you do not need to use the L^2 operator explicitly? How do you end up with your
sum(an* am <En|H|Em>) term?
 

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