Finding energy of a superposition of wavefunctions

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SUMMARY

The discussion focuses on a particle in an infinite square well described by a superposition of the ground state and first excited state wavefunctions, represented as ψ(x,0) = C[ψ_{1}(x) + ψ_{2}(x)]. It is established that this superposition is not a stationary state due to the differing energies of the components, E_{1} and E_{2}. However, the average energy of the superposition is confirmed to be the arithmetic mean of these energies, (E_{1} + E_{2})/2, demonstrating the concept of expectation value in quantum mechanics.

PREREQUISITES
  • Understanding of quantum mechanics principles, specifically wavefunctions and superposition.
  • Familiarity with the time-independent Schrödinger equation.
  • Knowledge of infinite square well potential and its energy eigenstates.
  • Basic grasp of expectation values in quantum systems.
NEXT STEPS
  • Study the derivation of energy eigenstates for the infinite square well potential.
  • Learn about the concept of expectation values in quantum mechanics.
  • Explore the implications of non-stationary states in quantum systems.
  • Investigate the role of superposition in quantum mechanics and its applications.
USEFUL FOR

Students of quantum mechanics, physics educators, and anyone interested in understanding the principles of wavefunction superposition and energy calculations in quantum systems.

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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-independent 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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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 Schrödinger equation.

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

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