Undergrad Harmonic Oscillator in 3D, different values on x, y and z

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In a 3D harmonic oscillator with different values for x, y, and z, the energy levels are defined by the equation E_{n1n2n3} = ħω1(n1 + 1/2) + ħω2(n2 + 1/2) + ħω3(n3 + 1/2). For the potential V(x,y,z) = 1/2mw²(x² + 4y² + z²), the frequencies are identified as ω1 = ω, ω2 = 2ω, and ω3 = ω. The first excited states correspond to E_{100} and E_{001}, both yielding the same energy of 3ħω, while E_{010} has a higher energy of 4ħω. The degeneracy of the first excited state is determined to be 2, as there are two states with equal energy. The discussion clarifies the relationship between the potential and the frequencies used in calculating energy levels.
Ofinns
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Hi,

For a harmonic oscillator in 3D the energy level becomes En = hw(n+3/2) (Note: h = h_bar and n = nx+ny+nz) If I then want the 1st excited state it could be (1,0,0), (0,1,0) and (0,0,1) for x, y and z.

But what happens if for example y has a different value from the beginning? Like this: V(x,y,z) = 1/2mw2(x2+4y2+z2) and for this decide the energy level AND degeneracy for the 1st excited state. I can only find simple examples when x, y and z are equal and 1.

Best regards
 
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In such a more general case you have
$$E_{n_1n_2n_3}=\hbar \omega_1 \left( n_1+\frac{1}{2} \right) + \hbar \omega_2 \left( n_2+\frac{1}{2} \right) + \hbar \omega_3 \left( n_3+\frac{1}{2} \right)$$
 
Demystifier said:
In such a more general case you have
$$E_{n_1n_2n_3}=\hbar \omega_1 \left( n_1+\frac{1}{2} \right) + \hbar \omega_2 \left( n_2+\frac{1}{2} \right) + \hbar \omega_3 \left( n_3+\frac{1}{2} \right)$$
Can you elaborate on that? Is 4y2 just n2 here? And in that case you will get three different energy values:

E100 = 3hw1/2
E010 =6hw2
E001 =3hw3/2

Which one is the 1st excited state? Is it E010?
 
Ofinns said:
Can you elaborate on that? Is 4y2 just n2 here?

No, it enters in as the frequency.
 
Ofinns said:
Can you elaborate on that?
In your case
$$\omega_1=w$$
$$\omega_2=2w$$
$$\omega_3=w$$
Therefore
$$E_{000}=2\hbar w$$
$$E_{100}=E_{001}=3\hbar w$$
$$E_{010}=4\hbar w$$
Hence the first excited states are ##E_{100}=E_{001}##.
 
Thank you, now I understand that part.

What will the degeneracy become for the 1st excited state then? Can I use the same formula gn = 1/2(n+1)(n+2) for this case?
 
Ofinns said:
What will the degeneracy become for the 1st excited state then?
It's 2.

Ofinns said:
Can I use the same formula gn = 1/2(n+1)(n+2) for this case?
No.
 
Demystifier said:
It's 2.

Why is it 2? What formula do you use to calculate that? (Sorry for all the questions..)
 
Ofinns said:
Why is it 2? What formula do you use to calculate that? (Sorry for all the questions..)
It follows from the last line of post #5. There you see that there are 2 "first excited states" with equal energies. Hence the degeneracy of first excited state is 2.
 
  • #10
Demystifier said:
It follows from the last line of post #5. There you see that there are 2 "first excited states" with equal energies. Hence the degeneracy of first excited state is 2.

Oh! Thank you so much for the answers, this has been bugging me for a while now.

Best regards
 
  • #11
Demystifier said:
In your case
$$\omega_1=w$$
$$\omega_2=2w$$
$$\omega_3=w$$

Late questions.. but why is w2=2w and not 4w?
 
  • #12
Ofinns said:
Late questions.. but why is w2=2w and not 4w?
Because, by definition,
$$V(x)=\frac{1}{2}m\omega^2 x^2$$
 
  • #13
Demystifier said:
Because, by definition,
$$V(x)=\frac{1}{2}m\omega^2 x^2$$

Right, of course. Thank you.
 

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