Why do uncertainty relations not apply in stationary states?

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Discussion Overview

The discussion centers on the nature of uncertainty relations in quantum mechanics, specifically the relationship between energy and position uncertainty in stationary states. Participants explore theoretical concepts and clarify distinctions between different types of uncertainty relations.

Discussion Character

  • Exploratory
  • Technical explanation
  • Conceptual clarification
  • Debate/contested

Main Points Raised

  • One participant seeks to understand why the energy-position uncertainty relation is considered meaningless in stationary states.
  • Another participant defines stationary states as wave functions with constant probability over time, suggesting a link to the uncertainty relations.
  • A participant elaborates on the differences between position-momentum uncertainty and energy-time uncertainty, noting that time is a parameter without an associated operator in quantum mechanics.
  • Concerns are raised about the interpretation of the energy-time uncertainty relation, with a suggestion that significant changes in expectation values require a superposition of energy eigenstates.
  • Clarifications are made regarding the definition of stationary states, emphasizing that they are represented by normalized eigenstates of the time-independent Hamiltonian.
  • Another participant agrees with the explanation provided, noting that stationary states contain only one energy value, which contributes to the understanding of uncertainty relations.
  • Discussion includes the idea that while the probability density of a stationary state is time-independent, it is not independent of position, and expectation values of observables are also time-independent.

Areas of Agreement / Disagreement

Participants express varying interpretations of the implications of stationary states on uncertainty relations, with no clear consensus reached on the nature of the energy-position uncertainty relationship.

Contextual Notes

Participants highlight the distinction between observables and parameters in quantum mechanics, particularly regarding the treatment of time in uncertainty relations. There is also mention of the need for superpositions in certain contexts, which may not be universally accepted.

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 probability 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 probability 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 [itex]E_{n} \in \sigma_{d}(\hat{H})[/itex])...

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 [tex]E_{i}[/tex]), 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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