QM: where did that energy come from?

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The discussion centers on the implications of measuring the position of an electron in a hydrogen atom and the resulting energy changes. When the position operator is applied, the wavefunction collapses into a Dirac delta function, leading to a probabilistic distribution across various orbitals. This measurement process disturbs the electron's state, potentially resulting in energy absorption or emission, as indicated by the interaction with a photon. The conversation highlights the quantum mechanical principles of measurement and the Heisenberg Uncertainty Principle, emphasizing the inherent disturbance caused by observation.

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koroljov
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This question is likely a stupid question, or based on some trivial misconception, but I can't find where the error is.

Imagine a hydrogen atom.
An electron is sitting nicely in its orbital. I measure its quantum numbers to know in which orbital it is. It will remain there for now, since the orbitals are eigenfunctions of the hamiltonian.

Now I decide to measure the position of the electron. So, I use the position operator (x,y,z). The eigenfunctions of this operator are Dirac functions (they are, aren't they?). So, the wavefunction now "collapses" into a dirac function. This dirac function can be expanded as a linear combination of the orbital functions (since these are orthonormal and complete).

So, when I measure the quantum numbers of the electron once again, I will have a nonzero chance of finding the electron in any of the orbitals which made a nonzero contribution to the expansion of the dirac function. Therefore, I might find the electron in an orbital with more or less energy than the one in which it was originally.

Where did that energy come from? Or, alternatively, where did it go to? Did I add or remove energy to/from the electron by trying to measure its position? Or is there some foolish error in the above reasoning?
 
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koroljov said:
This question is likely a stupid question, or based on some trivial misconception, but I can't find where the error is.

Imagine a hydrogen atom.
An electron is sitting nicely in its orbital. I measure its quantum numbers to know in which orbital it is. It will remain there for now, since the orbitals are eigenfunctions of the hamiltonian.

Now I decide to measure the position of the electron. So, I use the position operator (x,y,z). The eigenfunctions of this operator are Dirac functions (they are, aren't they?). So, the wavefunction now "collapses" into a dirac function. This dirac function can be expanded as a linear combination of the orbital functions (since these are orthonormal and complete).

So, when I measure the quantum numbers of the electron once again, I will have a nonzero chance of finding the electron in any of the orbitals which made a nonzero contribution to the expansion of the dirac function. Therefore, I might find the electron in an orbital with more or less energy than the one in which it was originally.

Where did that energy come from? Or, alternatively, where did it go to? Did I add or remove energy to/from the electron by trying to measure its position? Or is there some foolish error in the above reasoning?
If that atom were the only thing in the universe it could stay happily in its energy state, but you had to go and mess around with it, so it obviously is not the only thing in the universe. :smile: Somewhere in the course of your interaction with it, that atom absorbed or emitted a photon. Exactly how it does that involves more than just knowing about its electronic state wave functions.
 
koroljov said:
Imagine a hydrogen atom.
An electron is sitting nicely in its orbital. I measure its quantum numbers to know in which orbital it is. It will remain there for now, since the orbitals are eigenfunctions of the hamiltonian.
As I understand this situation

Measurement is an interaction with the wave function of the electron - proton combination that selects an eigenvalue of the measured quantum number (i.e. orbit number).

When you measure the orbital quantum number a photon interacts with the electron.
Therefore it will not remain there for now.

I took Quantum Mechanics in 1975 and do not work in the field.
But it seems to me that your idea of measurement is somewhat classical not Quantum Mechanical in this case and my be the cause of you concern.

The wave function contains all the information about a system.

But access to that information (selecting an eigenvalue of a quantum number) is probabilistic and disturbs its dual quantum number.
The dual quantum number is via the Hiedenberg Uncertainty Relation (measure one and the other is “spread”) momentum - position, time - energy etc.).
 

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