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According to quantum mechanics, the electron cloud for a hydrogen

atom in the ground state has a charge density

ÒÏ(r)=qττ²¹3e-2ra

where qis the charge of the electron and ais the Bohr radius. Find the atomic

polarizability of such an atom. [Hint:First calculate the electric field of the electron cloud, Ee(r) then expand the exponential, assuming r≪a.

Short Answer

Expert verified

The ground state electron cloud charge density is

isÒÏ(r)=qττa3e-2rais3πε0a3

Step by step solution

01

Given data

The electron cloud for a hydrogen atom in the ground state has a charge density

ÒÏ(r)=qÏ€a3e-2ra

02

Electric field on the surface of a Gaussian surface

The electric field on a spherical Gaussian surface of radius r is

E=Qenc4ττε0r2.....(1)

Here, Qencis the charge enclosed by the Gaussian surface.

03

Derivation of atomic polarizability

The expression for the charge enclosed inside the Gaussian surface is

Substitute the expression for ÒÏand get

Qenc=4πqπa3∫0re-2r'ar'2dr'=4qa3-a2e-2rar'2+ar'+a220r=q1-e-2ra1+2ra+2r2a2

Substitute this expression in equation (1) and get

Ee=14πε0r2q1-e-2ra1+2ra+2r2a2=14πε0r2q1-1-2ra+2r2a2-.....1+2ra+2r2a2=14πε0r2q43ra3+.....≈qr3πε0a3

But qr = p , the dipole moment of the atom.

The expression for atomic polarizability is

α=pE

Substitute the expressions in the above equation and get

α=qrqr3πε0a3=3πε0a3

Thus, the atomic polarizability is3πε0a3

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Most popular questions from this chapter

At the interface between one linear dielectric and another, the electric field lines bend (see Fig. 4.34). Show that

³Ù²¹²Ôθ2/³Ù²¹²Ôθ1=ε2/ε1

Assuming there is no free charge at the boundary. [Comment: Eq. 4.68 is reminiscent of Snell's law in optics. Would a convex "lens" of dielectric material tend to "focus’’ or "defocus," the electric field?]

A point charge Qis "nailed down" on a table. Around it, at radius R,

is a frictionless circular track on which a dipolep→ rides, constrained always to point tangent to the circle. Use Eq. 4.5 to show that the electric force on the dipole is

F→=Q4ττε0p→R3

Notice that this force is always in the "forward" direction (you can easily confirm

this by drawing a diagram showing the forces on the two ends of the dipole). Why

isn't this a perpetual motion machine?

A spherical conductor, of radius a,carries a charge Q(Fig. 4.29). It

is surrounded by linear dielectric material of susceptibilityXeout to radius b.Find the energy of this configuration (Eq. 4.58).

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 .

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··¡³¦´Ç²õθ

(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)»åΩ∫e-(u/kT)»åΩ

where »åΩ=²õ¾±²Ôθ»åθ»åÏ•, and the integration is over all orientations θ:0→π;Ï•:0→2Ï€Use 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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