Calculate d〈p〉/dt. Answer:

dpdx=-Vx

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

Short Answer

Expert verified

dpdx=-Vx

Schrodinger equation and its complex conjugate:

role="math" localid="1657778797745" ψt=ih2m2ψx2-ihVx,tψx,t1ψ*t=-ih2m2ψ*x2+ihVx,tψx,t2

And according to Ehrenfest’s theorem,

p=mv=mdxdt

Step by step solution

01

Determining the expectation value of x

Finding the expectation values.

x=-xψx.t2dx-ψx.t2dxx=-xψx.t2dxx=-ψx.tψ*x.tdxx=-ψx.tψ*x.tdx

02

Differentiating both the sides with respect to t,

dxdt=-ψx.tψx*x.tdxdxdt=-×ψtψx.tψ*x.tdxdxdt=-×ψtψ+ψ*ψtdx

03

Now, substituting the Schrodinger equation for the time derivatives

-X-ih2m2ψ*xψ+ihVψ*ψ+ih2mψ*2ψx2-ihVψ*ψdx

dxdt=ih2m-×ψ*2ψx2-2ψ*x2ψdx

dxdt=ih2m-×ψ*xψx2+ψ*2ψ2x2-2ψ2x2ψ+ψ*xψxdx

role="math" localid="1657786380532" dxdt=ih2m-×xψ*ψx-xψ*xψdx

dxdt=ih2m-×xψ*ψx-xψ*xψdxdxdt=ih2m×ψ*ψ---ψ*ψxdx--ψ*ψxdxdxdt=ih2m-ψ*ψxdx

Now, multiplying both sides by m

mdxdt=-ih-ψ*ψxdx

And using equation (3)

p=-ih-ψ*ψxdxp=-ψ*-ihxψdx

04

Differentiating both the sides with respect to t

We get the desired value,

dpdt=-ihddt-ψ*ψxdxdpdt=-ih-ψ*ψxdx
05

Using Clairaut’s theorem and substituting equation (1) and (2)

We get,

dpdt=-ih-ψ*tψt+ψ*xψtdxdpdt=-ih--ih2m2ψx2+ihVψ*ψx+ψ*xih2m2ψx2+ihVψdx
dpdt=-ih--ih2m2ψx2ψx+ihVψ*ψxih2mψ*3ψx3-ihVxψ*ψ-ihVψ*ψxdpdt=-ih--ih2mψ*xψx--ψx2ψx2dx+-ih2mψ3ψx3-ihVxψ*ψdx

localid="1657947924145" dpdt=-ih--ih2mψ*3ψx+ih2mψ*3x3-ihVXψ*ψdxdpdt=i2-VXψ*ψdx

dpdt=i2-Vxψ*ψdx

dpdt=--vxψ*ψdxdpdt=-ψ*-Vxψdxdpdt=-Vx

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Most popular questions from this chapter

Consider the Gaussian distribution

ρ(x)=Aeλ(xa)2

where A, a, and λ are positive real constants. (Look up any integrals you need.)

(a) Use Equation 1.16 to determine A.

(b) Find〈x〉,〈x2〉,and σ.

(c) Sketch the graph of ρ(x).

A particle of mass m is in the state:

ψ(x,t)=Aea[(mx2/h)+it]

where A and a are positive real constants.

(a) Find A.

(b) For what potential energy function, V(x), is this a solution to the Schrödinger equation?

(c) Calculate the expectation values of x,x2 , p, andp2 .

(d) Find σx and σp. Is their product consistent with the uncertainty principle?

Why can’t you do integration-by-parts directly on the middle expression in Equation -1.29 pull the time derivative over onto x, note thatx/t=0 , and conclude thatd<x>/dt=0 ?

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.

At time t = 0 a particle is represented by the wave function

ψ(x,0)={A(x,0),0xa,A(bx)/(ba),axb,0,otherwise,where A, a, and b are (positive) constants.

(a) Normalize ψ(that is, find A, in terms of a and b).

(b) Sketch ψ(x,0), as a function of x.

(c) Where is the particle most likely to be found, at t = 0?.

(d) What is the probability of finding the particle to the left of a? Check your result in the limiting cases b = a and b= 2a.

(e) What is the expectation value of x?

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