Finding energy of a superposition of wavefunctions

In summary, the conversation discusses a particle in an infinite square well and a wavefunction that is a superposition of two states with different energies. It is shown that this superposition is not a stationary state, but the average energy is the arithmetic mean of the two states. The use of the time-independent Schrodinger equation and the concept of expectation value is also mentioned.
  • #1
phosgene
146
1

Homework Statement



Consider a particle in an infinite square well described initially by a wave that is a superposition of the ground and first excited states of the well

[itex]ψ(x,0) = C[ψ_{1}(x) + ψ_{2}(x)][/itex]

Show that the superposition is not a stationary state, but that the average energy in this state is the arithmetic mean [itex](E_{1} + E_{2})/2[/itex] of the ground and first excited state energies [itex]E_{1}[/itex] and [itex]E_{2}[/itex].

Homework Equations



Time-independant Schroedinger equation (potential set to zero):

[itex]Eψ(x) = -\frac{\hbar^{2}∂^{2}}{2m∂x^{2}}[/itex]

The Attempt at a Solution



Assuming that the well is from x=0 to x=L, my wavefunction is [itex]ψ(x) = \sqrt{\frac{1}{L}}(sin(\frac{\pi x}{L}) + sin(\frac{2\pi x}{L}))[/itex]

Then using the Schroedinger equation

[itex]-\frac{\hbar^{2}∂^{2}}{2m∂x^{2}}\sqrt{\frac{1}{L}}(sin(\frac{\pi x}{L}) + sin(\frac{2\pi x}{L}))=Eψ(x)[/itex]

[itex]=\frac{\hbar^{2}}{2m}\sqrt{\frac{1}{L}}\frac{\pi ^{2}}{L^{2}}(sin(\frac{\pi x}{L}) + 4sin(\frac{2\pi x}{L}))[/itex]

But now I'm stuck because of the 4 in front of [itex]4sin(\frac{2\pi x}{L})[/itex]
 
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  • #2
Your wavefunction is a superposition of two states of different energies. So, your wavefunction does not have a definite energy and therefore will not itself be an eigenstate of the Hamiltonian (i.e., it's not a "stationary state"). So, your wavefunction will not satisfy the time-independent Schrodinger equation.

The average value of the energy for your wavefunction is the "expectation value" of the Hamiltonian for your wavefunction.
 
  • #3
Ah, I see. I'll give that a try. Thanks :)
 

Related to Finding energy of a superposition of wavefunctions

1. What is a superposition of wavefunctions?

A superposition of wavefunctions is a concept in quantum mechanics where multiple wavefunctions are combined to form a new, composite wavefunction. This composite wavefunction describes the probability of finding a particle in a certain state.

2. How is the energy of a superposition of wavefunctions calculated?

The energy of a superposition of wavefunctions is calculated by taking the weighted average of the energies of the individual wavefunctions. The weights are determined by the coefficients of the wavefunctions in the superposition.

3. Can the energy of a superposition of wavefunctions be negative?

Yes, the energy of a superposition of wavefunctions can be negative. This can occur when the individual wavefunctions have negative energies and the coefficients in the superposition have opposite signs.

4. How does the energy of a superposition of wavefunctions change over time?

The energy of a superposition of wavefunctions is constant over time if the individual wavefunctions have constant energies. However, if the individual wavefunctions have time-dependent energies, the energy of the superposition will also change over time.

5. Why is it important to find the energy of a superposition of wavefunctions?

Finding the energy of a superposition of wavefunctions is important because it is a fundamental aspect of quantum mechanics and can provide valuable information about the behavior of particles at the quantum level. It is also essential for understanding and predicting the behavior of complex quantum systems.

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