The postulate of Quantum Mechanics and Eigenvalue equation

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Discussion Overview

The discussion revolves around the postulates of quantum mechanics, specifically the relationship between measured observables and eigenvalues of linear Hermitian operators. Participants explore the implications of these postulates in idealized theoretical situations, particularly concerning the standard deviation of measurements and the nature of quantum states.

Discussion Character

  • Exploratory
  • Technical explanation
  • Debate/contested

Main Points Raised

  • One participant notes that according to quantum mechanics, every measured observable q is an eigenvalue of a corresponding operator Q, leading to the equation Qψ = qψ, but questions the implication that this necessitates a zero standard deviation σQ.
  • Another participant argues that real energy levels are characterized by uncertainty and that the postulates may not hold true in practical scenarios, distinguishing between Heisenberg uncertainty and measurement uncertainties.
  • A participant expresses confusion regarding the position of a harmonic oscillator, stating that the equation xψ = qψ suggests σx = 0, which they argue is incorrect since |ψ|² is not single-valued.
  • One participant clarifies that if a system is in an eigenstate of an observable, the measurement yields a corresponding eigenvalue with zero uncertainty, but if in a superposition, different results can occur, leading to non-zero σ.
  • Another participant reiterates the confusion about the standard deviation depending on the state and asks for clarification on the probability of measuring a specific eigenvalue q.

Areas of Agreement / Disagreement

Participants express various viewpoints regarding the implications of quantum mechanics postulates, particularly concerning standard deviations and the nature of measurements. There is no consensus on the interpretation of these concepts, and confusion remains evident among participants.

Contextual Notes

Participants highlight limitations in understanding related to the assumptions of idealized situations versus real-world measurements, as well as the complexities of quantum states and their implications for standard deviations.

betelgeuse91
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According to one of the postulates of quantum mechanics, every measured observable q is an eigenvalue of a corresponding linear Hermitian operator Q. Which means, that q must satisfy the equation Qψ = qψ. But according to Griffiths chapter 3, this equation can only be followed from σQ = 0. It makes no sense to me because not every observable has zero standard deviation. Can someone explain this?
 
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The exact energy levels (ferinstance) are for idealized situations... real energy levels are best characterised by a line with some thickness appropriate to the uncertainty of the state - which leads to it's stability. So you are learning that the postulates are not exactly true.

You also need to distinguish between uncertainties in the Heisenberg sense and measurement uncertainties arising from the way measurement equipment works.
Real life is messy.
 
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I am only considering idealized theoretical situations. The position of harmonic oscillator, for example, according to the postulate, a measured position value q is an eigenvalue of the equation xψ = qψ. But from this equation we can deduce that σx = 0. This is not true since |ψ|2 is not a single valued function. I am so confused...
 
betelgeuse91 said:
I am only considering idealized theoretical situations. The position of harmonic oscillator, for example, according to the postulate, a measured position value q is an eigenvalue of the equation xψ = qψ. But from this equation we can deduce that σx = 0. This is not true since |ψ|2 is not a single valued function. I am so confused...

The postulate says that if you measure a given observable, the result will be one of the eigenvalues of that observable. However, the system state is not necessarily an eigenstate before you measure; it may be a superposition of several different eigenstates with different eigenvalues and then your measurement may yield any of several different results. Formally, you prepare an ensemble of systems all in the same initial state and measure the observable on each instance. If the initial state is an eigenstate of the observable, you will get the corresponding eigenvalue on every measurement and ##\sigma## will be zero. However, if the initial state is a superposition you will get different results (all eigenvalues of one of the many eigenstates making up the superposition) on the different measurements and ##\sigma## will be non-zero.

For a number of reasons, it is not possible to prepare a system in an exact eigenstate of the position operator, so ##\sigma_x## will always be non-zero.
 
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betelgeuse91 said:
Can someone explain this?
The standard deviation depends on the state. In an eigenstate of ##Q##, there is no uncertainty about the value, so the standard deviation is zero, as it should be.
 
betelgeuse91 said:
I am only considering idealized theoretical situations. The position of harmonic oscillator, for example, according to the postulate, a measured position value q is an eigenvalue of the equation xψ = qψ. But from this equation we can deduce that σx = 0. This is not true since |ψ|2 is not a single valued function. I am so confused...
What they said... plus: what is the probability that a measurement of position will yeild the specific eigenvalue q? Explain how you worked it out so I can see your current understanding and I'll get back to you.

Note: the position operator has continuous eigenvalues, as does momentum.
The particular value for position is one of the allowed eigenvalues.
 

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