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Suppose you add a constantV0 to the potential energy (by “constant” I mean independent ofxas well as t). In classical mechanics this doesn’t change anything, but what about quantum mechanics? Show that the wave function picks up a time-dependent phase factor:exp(-iV0t/h). What effect does this have on the expectation value of a dynamical variable?

Short Answer

Expert verified

This constant will give the wave function a time-dependent phase factor. However, it will have no effect on the dynamical variables' expected values.

Step by step solution

01

The Schrödinger equation

The Schrödinger equation is given by,

ihψt=-h2m2ψX2+ …… (1)

This equation is without a constant V0.

02

Schrödinger equation after adding constant V0

If a constant is added to the potential energy, the Schrödingerequation will be,

ihψt=-h2m2ψX2+(V+V0)ψ …… (2)

A time-dependent phase factor will be picked up by the wave function that is e-N0t/h. For doing the calculation a new wave function ϕwill be taken that is equal to the old wavefunction which is multiplied with the phase factor.

Φ=ψe-iv0t/h

03

Replacement of first equation with wave function

Now, equation (1) will be replaced with this new wave function (the originalSchrödingerequation before adding the constant to the potential energy). So, the equation will be:

ihΦt=-h2m2ΦX2+VΦihΦtψe-iv0t/h=-h2m2X2ψe-iv0t/h+Vψe-iv0t/hihψte-iv0t/h+ψV0e-iv0t/h=-h2m2ψX2e-iv0t/h+Vψe-iv0t/hihψt=-h2m2ψX2+Vψ-ψV0ihψt=-h2m2ψX2+(V+V0)ψ

04

Calculating the expectation value of a particle using the new potential energy

The negative sign is absorbed into the constant in this case. The extra phase factor will also have no effect on the dynamical variables' expected values.

Q=-ϕ*Qx,-ihXϕdxQ=-ψe-iv0t/h*Qx,-ihXψe-iv0t/hdxQ=-ψe-iv0t/hQx,-ihXψe-iv0t/hdxQ=-ψ*Qx,-ihXψdx

Because the dynamical variables do not depend on time (just on position), the extra phase component will have no effect on the dynamical variables' expected value.

Hence, it’s the same as the old potential energy.

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Most popular questions from this chapter

In general, quantum mechanics is relevant when the de Broglie wavelength of the principle in question(h/p)is greater than the characteristic Size of the system (d). in thermal equilibrium at (kelvin) TemperatureTthe average kinetic energy of a particle is

p22m=32kBT

(Where kBis Boltzmann's constant), so the typical de Broglie wavelength is

λ=h3mkBT

The purpose of this problem is to anticipate which systems will have to be treated quantum mechanically, and which can safely be described classically.

(a) Solids. The lattice spacing in a typical solid is around d=0.3nm. Find the temperature below which the free 18electrons in a solid are quantum mechanical. Below what temperature are the nuclei in a solid quantum mechanical? (Use sodium as a typical case.) Moral: The free electrons in a solid are always quantum mechanical; the nuclei are almost never quantum mechanical. The same goes for liquids (for which the interatonic spacing is roughly the same), with the exception of helium below 4K.

(b) Gases. For what temperatures are the atoms in an ideal gas at pressure Pquantum mechanical? Hint: Use the ideal gas law(PV=NkBT)to deduce the interatomic spacing.

In general, quantum mechanics is relevant when the de Broglie wavelength of the principle in question(h/p) is greater than the characteristic Size of the system (d). in thermal equilibrium at (kelvin) TemperatureT the average kinetic energy of a particle is

p22m=32kBT

(Where kBis Boltzmann's constant), so the typical de Broglie wavelength is

λ=h3mkBT.

The purpose of this problem is to anticipate which systems will have to be treated quantum mechanically, and which can safely be described classically.

(a) Solids. The lattice spacing in a typical solid is aroundd=0.3nm . Find the temperature below which the free 18electrons in a solid are quantum mechanical. Below what temperature are the nuclei in a solid quantum mechanical? (Use sodium as a typical case.) Moral: The free electrons in a solid are always quantum mechanical; the nuclei are almost never quantum mechanical. The same goes for liquids (for which the interatonic spacing is roughly the same), with the exception of helium below4K .

(b) Gases. For what temperatures are the atoms in an ideal gas at pressure quantum mechanical? Hint: Use the ideal gas law (PV=NkBT)to deduce the interatomic spacing.

(a) Find the standard deviation of the distribution in Example 1.1.

(b) What is the probability that a photograph, selected at random, would show a distance x more than one standard deviation away from the average?

Calculate d〈p〉/dt. Answer:

dpdx=-Vx

This is an instance of Ehrenfest’s theorem, which asserts that expectation values obey the classical laws

Question: Let pab(t)be the probability of finding a particle in the range (a<x<b),at time t.

(a)Show that

dpabdt=j(a.t)-j(b,t),

Where

j(x,t)ih2m(ψψ*x-ψ*ψx)

What are the units of j(x,t)?

Comment: j is called the probability current, because it tells you the rate at which probability is "flowing" past the point x. Ifpab(t) is increasing, then more probability is flowing into the region at one end than flows out at the other.

(b) Find the probability current for the wave function in Problem 1.9. (This is not a very pithy example, I'm afraid; we'll encounter more substantial ones in due course.)

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