Why do uncertainty relations not apply in stationary states?

RPI_Quantum
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I am trying to understand the nature of uncertainty relations in quantum mechanics. I am looking specifically at a relation between energy and position uncertainty... the book that I am reading hints that this relationship has no meaning in a stationary state. Why would that be?
 
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Maybe if I were to say that a Sationary state (eigenstate) is a wave function who's probablity is constant through time? Take a look thorugh here: http://www.chemistry.ohio-state.edu/betha/qm/
 
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Thanks

Yes that did help a lot. However, I think I am still missing something. I understand that in the stationary state nothing changes with time. Yet, I do not quite see how this makes the uncertainty relationship between energy and position any different from the one between position and momentum. Maybe if you could elaborate on how the constant probability effects this uncertainty relation...

Thanks for the link by the way. I didn't search through it entirely yet, but many questions that I have been having were certainly addressed in it.
 
RPI_Quantum said:
Yes that did help a lot. However, I think I am still missing something. I understand that in the stationary state nothing changes with time. Yet, I do not quite see how this makes the uncertainty relationship between energy and position any different from the one between position and momentum.

In non-relativistic QM, there is difference in nature between the x-p uncertainty and the E-t uncertainty.
x and p are observables, so they both are results of measurements in NR QM ; the uncertainty principle just gives you a property of their probability distributions (namely that the product of their standard variations has a lower bound).
E is also an observable, but time (t) is a parameter. There is NO T - operator or T observable in QM. So you cannot talk about "an uncertainty in time" as the standard deviation of the probability distribution of t.

But what then does the E - t "uncertainty" relation mean ?

It actually means that if you want to have significant changes in the expectation values of ANY observable within a time lapse dt, then you need to have a superposition of several energy eigenstates such that the standard deviation of the energy measurement becomes at least dE, with
dt . dE > hbar/2

cheers,
Patrick.
 
I would just like to add that your posts are very clear and helpful, Patrick!
 
RPI_Quantum,

Does your "RPI" stand for "Rennselaer Polytechnic Institute"?

I went to RPI, and I now teach at HVCC. Hi! :smile:
 
DB said:
Maybe if I were to say that a Sationary state (eigenstate) is a wave function who's probablity is constant through time? Take a look thorugh here: http://www.chemistry.ohio-state.edu/betha/qm/

That's an inexact formulation of a property of the stationary states,not exactly the DEFINITION.Stationary states in the standard formulation are described through NORMALIZED EIGENSTATES OF THE TIME-INDEPENDENT HAMILTONIAN (Schroedinger picture) ASSOCIATED TO EIGENVALUES (denoted generally by E_{n} \in \sigma_{d}(\hat{H}))...

What wave function and what probability are u talking about...??


Daniel.
 
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Indeed the post of Vanesch explains everything and it is very well written. Now if you just realized that a stationary state is represented by a wavefunction with only ONE energy-value in it (not a superposition of several energy values E_{i}), it is quite straightforward to see that the uncertainty-relations do not apply here. Just focus on the example that Vanesch gave as to explain the uncertainty between both E and t

regards
marlon

ps : indeed, the probability density of a stationary state is independent of time but NOT position and the expectation value of any observable (provided the observable is independent of t itself) is also independent of time BUT NOT position.
 
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