Chapter 2: Q25P (page 77)
Check the uncertainty principle for the wave function in the equation? Equation 2.129.
Short Answer
Uncertainty of the wave equation
Chapter 2: Q25P (page 77)
Check the uncertainty principle for the wave function in the equation? Equation 2.129.
Uncertainty of the wave equation
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Get started for freeThis is a strictly qualitative problem-no calculations allowed! Consider the "double square well" potential (Figure 2.21). Suppose the depth and the width a are fixed, and large enough so that several bound states occur.
(a) Sketch the ground state wave function and the first excited state localid="1658211858701" (i) for the case b = 0 (ii) forand (iii) for
(b) Qualitatively, how do the corresponding energiesand vary, as b goes from 0 to ? Sketch and on the same graph.
(c) The double well is a very primitive one-dimensional model for the potential experienced by an electron in a diatomic molecule (the two wells represent the attractive force of the nuclei). If the nuclei are free to move, they will adopt the configuration of minimum energy. In view of your conclusions in (b), does the electron tend to draw the nuclei together, or push them apart? (Of course, there is also the internuclear repulsion to consider, but that's a separate problem.)
Solve the time-independent Schr ̈odinger equation for a centered infinite square well with a delta-function barrier in the middle:
Treat the even and odd wave functions separately. Don’t bother to normalize them. Find the allowed energies (graphically, if necessary). How do they compare with the corresponding energies in the absence of the delta function? Explain why the odd solutions are not affected by the delta function. Comment on the limiting cases α → 0 and α → ∞.
Calculate ,for the nth stationary state of the infinite square well. Check that the uncertainty principle is satisfied. Which state comes closest to the uncertainty limit?
Although the overall phase constant of the wave function is of no physical significance (it cancels out whenever you calculate a measurable quantity), the relative phase of the coefficients in Equation 2.17 does matter. For example, suppose we change the relative phase of in problem 2.5:Where is some constant. Find , and , and compare your results with what you got before. Study the special cases .
In the ground state of the harmonic oscillator, what is the probability (correct to three significant digits) of finding the particle outside the classically allowed region?
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