Expectation value of energy for a quantum system

In summary: However, in this case, I am assuming the derivative is zero so I use ##\int \Psi^* \hat{H} \Psi dx## and obtain the expected average of energy.
  • #1
CAF123
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Homework Statement


Let ##\Psi(x,0)## be the wavefunction at t=0 described by ##\Psi(x,0) = \frac{1}{\sqrt{2}}\left(u_1(x) + u_2(x)\right)##, where the ##u_i## is the ##ith## eigenstate of the Hamiltonian for the 1-D infinite potential well.

The energy of the system is measured at some t - what are are the possible outcomes of such a measurement?
Find the average energy of the system as a function of time. Does this value depend on the initial state of the system?

Homework Equations


Average value of energy, ##\langle H \rangle##

The Attempt at a Solution


Since the 1D Infinite well represents a discrete spectrum of eigenvalues, I would say that the only possible values of the energy are E1 and E2. However, to see this I considered the probabilities of obtaining such energies: For E1, it is given by ##\langle u_1 | \Psi \rangle ##and this gives ##\frac{1}{2} e^{-Kt}## where K is some numerical factor. Similarly for probability of E2: ##\frac{1}{2}e^{-K't}##. This suggests at t=0, the probability of getting a particular Ei, i either 1 or 2 is 1/2, but that this decays exponentially. How should I interpret this? At some finite t, P(E1) + P(E2) is not 1, so does this mean there exists another possible energy?

I think I may compute the average energy as ##\langle H \rangle = \int dx H |\Psi(x,t)|^2##. Since it says '...find this as a function of time, this suggests there is more to the first part since if at any time t, we could get E1 or E2 with equal probability, then this would suggest the average energy would be (E1+E2)/2 ≠ f(t).

Many thanks.
 
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  • #2
K should be purely imaginary, so the probability (as squared magnitude) should be constant.

The average energy just follows from the probabilities to find states 1 and 2.
 
  • #3
mfb said:
K should be purely imaginary, so the probability (as squared magnitude) should be constant.
I see, okay it makes sense now.

The average energy just follows from the probabilities to find states 1 and 2.
The average energy, although I could do the integral ##\int H |\Psi(x,t)|^2dx## physically I already know that the answer will be (E1+E2)/2, which is not a function of time. So at all times in the motion, the average energy is time independent. In answering the last question, I think this would depend on the initial state - if you had the initial w. f as a superposition of other e. states then the average energy would not be simply the average of the energy eigenvalues corresponding to the lowest e. states. Is this right?
 
  • #5
mfb said:
Right.
Thank you, I have derived the average position of the particle to be the following: $$\langle x \rangle = \frac{a}{2}\left(1 - C \cos (Pt ) \right)$$

This has been confirmed correct. Classically, we expect average position to be a/2. Quantum mechanically, there is this second oscillatory term. Can we gain any insight into why this term is here?

Also, in the calculation of the average energy, ##(\int H |\Psi(x,t)|^2dx)## I take the Hamiltonian to be ##-\frac{\hbar^2}{2m} \frac{d^2}{dx^2}## simply right? When I use this, I end up with 0, which I confirmed with Wolfram alpha. However, I am not sure if I should be using ##\hat{H} \mapsto i\hbar \frac{\partial}{\partial t}## or not.
 
Last edited:
  • #6
Classically, the expectation value for a specific t is just the position of the particle at that time. In general, the particle will move inside the potential well, so you get some oscillation as well (just not with a cos, but with linear motion).
I think you mean the average over time - in this case, both classical an QM calculation give a/2.

The Hamiltonian inside the well? How did you get that formula?
What do you mean with ##\hat{H} \mapsto i\hbar \frac{\partial}{\partial t}##?
 
  • #7
mfb said:
Classically, the expectation value for a specific t is just the position of the particle at that time. In general, the particle will move inside the potential well, so you get some oscillation as well (just not with a cos, but with linear motion).
I think you mean the average over time - in this case, both classical an QM calculation give a/2.
Classically, it is clear that the average is a/2. The particle's position is a uniform random variable with a constant probability density. I don't see yet why this average is the same in the QM calculation. The average of x I got was precisely the form with the cos term.

The Hamiltonian inside the well? How did you get that formula?
Generally ##\hat{H} = \frac{\hat{P}^2}{2m} + V(\hat{X})## The second term vanishes inside the well and I use ##\hat{P} \mapsto -i\hbar \frac{d}{dx}##. Actually, I found my mistake, the formula I quoted is not quite correct because the Hamiltonian has a derivative so I used ##\int \Psi^* \hat{H} \Psi dx## and obtained the expected average of energy.
What do you mean with ##\hat{H} \mapsto i\hbar \frac{\partial}{\partial t}##?
I have seen forms of the Hamiltonian where it is represented by ##i \hbar \frac{\partial}{\partial t}## and that as written above. Are these two forms equivalent and where did the first one come from?
 
  • #8
CAF123 said:
Classically, it is clear that the average is a/2. The particle's position is a uniform random variable with a constant probability density. I don't see yet why this average is the same in the QM calculation. The average of x I got was precisely the form with the cos term.
You are comparing two different averages here.
For the classical particle, you average over time, for the QM particle you do not. The results are different, but that shouldn't be surprising.


I have seen forms of the Hamiltonian where it is represented by ##i \hbar \frac{\partial}{\partial t}## and that as written above. Are these two forms equivalent and where did the first one come from?
That looks like it is coming from the Schroedinger equation. They are not the same, but acting on the wavefunction they should give the same result.
 
  • #9
mfb said:
You are comparing two different averages here.
For the classical particle, you average over time, for the QM particle you do not. The results are different, but that shouldn't be surprising.
So what does my calculation of <x> actually really represent then? I see that it cannot be the average of position over time since time is still a factor in my expression for <x>.
 
  • #10
CAF123 said:
So what does my calculation of <x> actually really represent then? I see that it cannot be the average of position over time since time is still a factor in my expression for <x>.
It is the expectation value of the position at a specific time - the average over many measurements of copies of the same system, if you like.
 
  • #11
mfb said:
It is the expectation value of the position at a specific time - the average over many measurements of copies of the same system, if you like.
It makes sense, thanks. So how would I find the average over time, that is how could I show that the average position over time is a/2?
 
  • #12
Average over one period of the cos.
 
  • #13
mfb said:
Average over one period of the cos.
So like $$\frac{1}{P} \int_{0}^{\frac{2 \pi}{P}} \langle x \rangle\,dt?$$
 
  • #14
That looks good.
Here, you don't need an integral, it is sufficient to know that the cos function has an average value of zero.
 

What is the expectation value of energy for a quantum system?

The expectation value of energy for a quantum system is a measure of the average energy that the system is expected to have when measured. It takes into account all possible energy states and their probabilities.

How is the expectation value of energy calculated for a quantum system?

The expectation value of energy is calculated by taking the sum of the products of each energy state and its corresponding probability. Mathematically, it is represented as Σ(E_n * P_n), where E_n is the energy of the nth state and P_n is the probability of the system being in that state.

What does the expectation value of energy tell us about a quantum system?

The expectation value of energy provides us with information about the average energy of a quantum system. It can help us understand the overall behavior and stability of the system and make predictions about its future energy states.

How does the expectation value of energy relate to the uncertainty principle?

The expectation value of energy and the uncertainty principle are closely related. According to the uncertainty principle, it is impossible to know the exact energy of a quantum system at a given time. The expectation value of energy takes into account this uncertainty and provides us with a more realistic understanding of the system.

Can the expectation value of energy change over time for a quantum system?

Yes, the expectation value of energy can change over time for a quantum system. This is because the probabilities of the energy states can change as the system evolves, leading to a different average energy value. However, the total energy of the system will remain constant.

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