Another energy eigenvalue question

In summary, you came up with a complex exponential function to solve for the eigenvalue equation and missed the kinetic energy term.
  • #1
Isaac0427
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Take the wavefunction $$e^{-i\omega t}$$ which all time dependent functions can be superposed of (right?). You can then get $$ih\frac{\partial}{\partial t}\psi=\hbar \omega \psi$$ and thus if ##\hat{E}=ih\frac{\partial}{\partial t}## then $$\hat{E}\psi=E\psi$$ What did I do wrong?
 
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  • #2
What's your question actually?
Moreover, this doesn't seem like a quantum mechanics problem. You don't even need ##\hbar## as it can be canceled out and the ##\nabla^2## term is also missing, it's just a math eigenvalue problem.
 
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  • #3
blue_leaf77 said:
What's your question actually?
Moreover, this doesn't seem like a quantum mechanics problem. You don't even need ##\hbar## as it can be canceled out and the ##\nabla^2## term is also missing, it's just a math eigenvalue problem.
I know from previous threads that ##\hat{E} \psi =E\psi## is not a correct QM equation, yet I just "derived" it. What did I do wrong?
 
  • #4
I don't know which thread you refer to but the general form of the Schroedinger equation is
$$
i\hbar \frac{\partial}{\partial t} \psi(\mathbf{r},t) = H(\mathbf{r},t) \psi(\mathbf{r},t)
$$
It may reduce to the time independent Schroedinger equation when the Hamiltonian is time-independent and ##\psi## is an eigenfunction of the Hamiltonian.
However, the equation you have there is not a Schroedinger equation since it misses the kinetic energy term.
 
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  • #5
blue_leaf77 said:
I don't know which thread you refer to but the general form of the Schroedinger equation is
$$
i\hbar \frac{\partial}{\partial t} \psi(\mathbf{r},t) = H(\mathbf{r},t) \psi(\mathbf{r},t)
$$
It may reduce to the time independent Schroedinger equation when the Hamiltonian is time-independent and ##\psi## is an eigenfunction of the Hamiltonian.
However, the equation you have there is not a Schroedinger equation since it misses the kinetic energy term.
Would my equation work?
 
  • #6
Your equation is mathematically correct: you come up with a complex exponential function and construct an eigenvalue equation that it satisfies, but this eigenvalue equation is not a Schroedinger equation.
 
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  • #7
blue_leaf77 said:
Your equation is mathematically correct: you come up with a complex exponential function and construct an eigenvalue equation that it satisfies, but this eigenvalue equation is not a Schroedinger equation.
So this equation is correct for time dependent quantum systems, right? And because ##\hat{H}=\frac{\hat{p}^2}{2m}+V(\hat{x})##, for stationary states we get ##\hat{H}\psi=E\psi## and for time dependent systems we get ##\hat{H}\psi=\hat{E}\psi##. Is that correct?
 
  • #8
Isaac0427 said:
So this equation is correct for time dependent quantum systems, right?
There is nothing which can be associated with a quantum system since your equation is not a Schroedinger equation.
Isaac0427 said:
for time dependent systems we get ^Hψ=^EψH^ψ=E^ψ\hat{H}\psi=\hat{E}\psi. Is that correct?
Time-dependent system is known to be difficult to solve analytically. Most time-dependent cases are dealt with the help of some perturbation theory. I can't be certain myself that a concept of eigenstates also applies in TDSE. There is probably not even a stationary state, take for example the time evolution of states in a time-dependent Hamiltonian in which the Hamiltonian in any given time commutes with the Hamiltonian at other times. The time evolution reads
$$
\psi(x,t) = \exp\left( -\frac{i}{\hbar} \int_0^t H(t') dt' \right) \psi(x,0)
$$
I don't see how states that evolve that way can yield time-independent expectation value for any observable for this state to deserve the calling "stationary".
 
  • #9
Well, the Schrödinger equation indeed reads
$$\mathrm{i} \hbar \partial_t \psi(t,\vec{x})=\hat{H} \psi(t,\vec{x}).$$
The equation can be separated in the form
$$\psi(t,\vec{x})=T(t) \Psi(\vec{x}),$$
if the Hamiltonian is not time dependent, because then
$$\mathrm{i} \hbar \partial_t \psi = \mathrm{i} \hbar \dot{T}(t) \Psi(\vec{x})= T(t) \hat{H} \Psi(\vec{x}).$$
Now divide this equation by ##T(t) \Psi(\vec{x})##. Then you get
$$\frac{1}{T}(t) \mathrm{i} \hbar \dot{T}(t) =\frac{1}{\Psi(\vec{x})} \hat{H} \Psi(\vec{x}).$$
Now, since the left-hand side is independent of ##\vec{x}## and the right-hand-side is independent of ##t##, it must be a constant, which we call ##E##. This implies the equation for ##T##
$$\mathrm{i} \hbar \dot{T}=E T \; \Rightarrow \; T(t)=T_0 \exp(-\mathrm{i} \omega t), \quad \omega=\frac{E}{\hbar},$$
and for ##\Psi##:
$$\hat{H} \Psi(\vec{x})=E \Psi(\vec{x}),$$
i.e., ##\Psi## must be an eigenvector of ##\hat{H}## which of course is NOT ##\mathrm{i} \hbar \partial_t## but some differential operator in ##\vec{x}## like the standard case for the motion of a particle in some external potential,
$$\hat{H}=-\frac{\hbar^2}{2m} \Delta + V(\vec{x}).$$
So the general solution of the time-dependent Schrödinger equation can be written in terms of the energy-eigensolutions (i.e., the solutions of the time-independent Schrödinger equation)
$$\psi(t,\vec{x})=\sum_{E} a_E \exp(-\mathrm{i} \omega t) \Psi_E(\vec{x}), \quad \hat{H} \Psi_E(\vec{x})=E \Psi_E(\vec{x}).$$
The sum goes over all energy eigenvalues. If there are continuous energy eigenvalues ("scattering solutions"), there's also an integral over the corresponding values. Of course, there are cases, where the Hamiltonian has only a continuous spectrum, as in the case of the free particle.
 
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  • #10
@vanhees71 , I think you missed the expansion coefficient (which might as well be dependent on time) in the last equation containing the sum.
 
  • #11
True. I've corrected it, but it must of course be time independent. It's given by the initial wave function at ##t=t_0##.
 
  • #12
vanhees71 said:
So the general solution of the time-dependent Schrödinger equation
I thought you were deriving the general form of the wavefunction arising from a time dependent Hamiltonian. If the expansion coefficient is not a function of time, wouldn't ##\psi(t,\vec{x})## as you wrote above just the solution of a Schroedinger equation with a time-independent Hamiltonian. It's just the time evolution operator ##U(t,t_0)## applied to the initial state ##\psi(t_0,\vec{x}) = \sum_E a_E \psi_E(t_0,\vec{x})##. That ##a_E## for time dependent Hamiltonian should be a function of time, you can look at equation 5.5.4 in Modern Quantum Mechanics by Sakurai.
 
  • #13
Yes, sure, for a time-dependent Hamiltonian (in the Schrödinger picture of time evolution!) you cannot separate the Schrödinger equation anymore, and the energy eigenvectors become time-dependent and thus also the expansion coefficients.
 
  • #14
Ah sorry I misread
vanhees71 said:
time-dependent Schrödinger equation
as "time-dependent Hamiltonian".
 

Related to Another energy eigenvalue question

1. What is an energy eigenvalue?

An energy eigenvalue is a value that represents the total energy of a system in quantum mechanics. It is a characteristic of the system and is found by solving the Schrödinger equation.

2. How is an energy eigenvalue calculated?

An energy eigenvalue is calculated by solving the Schrödinger equation, which is a mathematical equation that describes the behavior of quantum systems. The solution to this equation gives the possible values of energy that the system can have.

3. What is the significance of energy eigenvalues in quantum mechanics?

Energy eigenvalues are significant in quantum mechanics because they represent the possible energy states of a system. They also play a role in determining the probabilities of different energy levels in a system.

4. Can energy eigenvalues have negative values?

Yes, energy eigenvalues can have negative values. In quantum mechanics, energy is a relative concept and negative energy values can arise in certain systems or interactions.

5. How do energy eigenvalues relate to energy levels?

Energy eigenvalues correspond to the energy levels of a system. Each energy eigenvalue represents a specific energy level that the system can have. The higher the energy eigenvalue, the higher the energy level of the system.

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