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According to Eq. 4.1, the induced dipole moment of an atom is proportional to the external field. This is a "rule of thumb," not a fundamental law,

and it is easy to concoct exceptions-in theory. Suppose, for example, the charge

density of the electron cloud were proportional to the distance from the center, out to a radius R.To what power of Ewould pbe proportional in that case? Find the condition on such that Eq. 4.1 will hold in the weak-field limit.

Short Answer

Expert verified

The dipole moment of a charge density proportional to the distance from the centre is proportional to the square root of the electric field. For the electric field to be directly proportional to the dipole moment, the charge density has to be constant.

Step by step solution

01

Given data

The charge density of the electron cloud is

ρ=Ar.....(1)

Here, Ais the proportionality constant and r is the distance from the centre.

02

Electric field on a spherical Gaussian surface

The electric field on the a spherical Gaussian surface of radius ris

E=Qenc4ττε0r2......(2)

Here, Qencis the charge enclosed by the Gaussian surface.

The infinitesimal volume element in spherical polar coordinates with just radial dependence is

=4ττr2dr.....(3)

03

Derivation of dipole moment in terms of electric field

The expression for the charge enclosed is

Qenc=0rρr'dτ'

Substitute the expression for the charge density from equation (1) and volume element from equation (3)

Qenc=4π0rAr'r'2dr'=πAr4

Substitute expression for Qencin equation (2)

E=14πε0r2πAr4=Ar24ε0

Rearranging this

r=4ε0EA

The expression for the dipole moment is

p=qr

Substitute the expression for rand get

p=q4εEA

Thus, the dipole moment is proportional to E.

For the electric field to be proportional to the dipole moment, the electric field has to be proportional to r. Thus, the charge density has to be constant.

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Most popular questions from this chapter

Question: A sphere of linear dielectric material has embedded in it a uniform

free charge density . Find the potential at the center of the sphere (relative to

infinity), if its radius is R and the dielectric constant is r.

The space between the plates of a parallel-plate capacitor is filled

with dielectric material whose dielectric constant varies linearly from 1 at the

bottom plate (x=0)to 2 at the top plate (x=d).The capacitor is connectedto a battery of voltage V.Find all the bound charge, and check that the totalis zero.

According to Eq. 4.5, the force on a single dipole is (p · V)E, so the

netforce on a dielectric object is

F=P·Eextdτ

[Here Eextis the field of everything except the dielectric. You might assume that it wouldn't matter if you used the total field; after all, the dielectric can't exert a force on itself. However, because the field of the dielectric is discontinuous at the location of any bound surface charge, the derivative introduces a spurious delta function, and it is safest to stick withEext Use Eq. 4.69 to determine the force on a tiny sphere, of radius , composed of linear dielectric material of susceptibility χewhich is situated a distance from a fine wire carrying a uniform line chargeλ .

A short cylinder, of radius a and length L, carries a "frozen-in" uniform polarization P, parallel to its axis. Find the bound charge, and sketch the electric field (i) for La, (ii) for La, and (iii) for La. [This is known as a bar electret; it is the electrical analog to a bar magnet. In practice, only very special materials-barium titanate is the most "familiar" example-will hold a permanent electric polarization. That's why you can't buy electrets at the toy store.]

The Clausius-Mossotti equation (Prob. 4.41) tells you how to calculatethe susceptibility of a nonpolar substance, in terms of the atomic polariz-ability. The Langevin equation tells you how to calculate the susceptibility of apolar substance, in terms of the permanent molecular dipole moment p. Here's howit goes:

(a) The energy of a dipole in an external field E isu=-p·Ecosθ

(Eq. 4.6), whereθ is the usual polar angle, if we orient the z axis along E.

Statistical mechanics says that for a material in equilibrium at absolute temperature

T, the probability of a given molecule having energy u is proportional to

the Boltzmann factor,

exp(-u/kT)

The average energy of the dipoles is therefore

<u>=ue-(u/kt)e-(u/kT)

where =sinθdθdϕ, and the integration is over all orientations θ:0π;ϕ:02πUse this to show that the polarization of a substance

containing N molecules per unit volume is

P=Np[cothpE/kT-kT/pE] (4.73)

That's the Langevin formula. Sketch as a function ofPE/KT .

(b) Notice that for large fields/low temperatures, virtually all the molecules arelined up, and the material is nonlinear. Ordinarily, however, kT is much greaterthan p E. Show that in this regime the material is linear, and calculate its susceptibility,in terms of N, p, T, and k. Compute the susceptibility of water at 20°C,and compare the experimental value in Table 4.2. (The dipole moment of wateris 6.1×10-30C·m) This is rather far off, because we have again neglected thedistinction between E and Eelse· The agreement is better in low-density gases,for which the difference between E and Eelse is negligible. Try it for water vapor

at 100°C and 1 atm.

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