Finding energy of a superposition of wavefunctions

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The discussion centers on a particle in an infinite square well with an initial wavefunction as a superposition of the ground and first excited states. It is established that this superposition is not a stationary state due to the differing energies of the components, meaning it does not satisfy the time-independent Schrödinger equation. The average energy of the superposition state is calculated to be the arithmetic mean of the energies of the ground state and the first excited state, represented as (E1 + E2)/2. The conversation highlights the importance of understanding expectation values in quantum mechanics. Overall, the key takeaway is the distinction between stationary states and superpositions in terms of energy and time evolution.
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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

ψ(x,0) = C[ψ_{1}(x) + ψ_{2}(x)]

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

Homework Equations



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

Eψ(x) = -\frac{\hbar^{2}∂^{2}}{2m∂x^{2}}

The Attempt at a Solution



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

Then using the Schroedinger equation

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

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

But now I'm stuck because of the 4 in front of 4sin(\frac{2\pi x}{L})
 
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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 Schrodinger 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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