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Suppose we put a delta-function bump in the center of the infinite square well:

H'=αδ(x-a/2)

whereais a constant.

(a) Find the first-order correction to the allowed energies. Explain why the energies are not perturbed for evenn.

(b) Find the first three nonzero terms in the expansion (Equation 6.13) of the correction to the ground state,Ψ11.

Short Answer

Expert verified

The first-order correction to the allowed energies=2αasin22

The the first three nonzero terms in the expansion of the correction to the ground state,Ψ11is=a2π2ħ2sin3πxa-13sin5πxa+16sin7πxa

Step by step solution

01

Stationary state of a one-dimensional infinite square well.

The stationary state of a one-dimensional infinite square wellis:

Ψn0=2asin(ax)

02

Step 2: The first-order correction to the allowed energies.

a)

For the infinite square well:

H^'=αδx-a2,α=const

Solve the problem by considering the stationary state of a one-dimensional infinite square well, that is:Ψn0=2asinaxEn'=Ψn0H^'Ψn0=0aH^'Ψ^n0dX=2αa0aδx-a2sin2nπxadx=2αa2sina.a2=2αasin22-fornoddEn,=2αasin22=2αa-fornevenEn'=0

03

Step 3: The first three nonzero terms in the expansion.

b)

Use the formula and substitute each value.

Ψn1=mnΨn0H^'Ψn0En0-Em0Ψm0

For n=1

Ψn0H^'Ψn0=2αa0adxsinmπxaδx-a2sinπxa=2αasina.a2sinπa.a2=2αasin2

Note that:m1,n=1,mn

form=0sin0=0

form=0sin=0

The first three non- zero terms (odd)

m=3,5,7;n=1En0=n2π2ħ2ma2E10=π2ħ22ma2Ψ11=2aa2asin3π2π2ħ22ma21-9sin3πxa+sin5π2sin5πxaπ2ħ22ma21-25+sinin5π2sin5πxaπ2ħ22ma21-49=2aa2a2ma2π22ma2π2ħ218sin3πxa-124sin5πxa+148sin7πxa

Proceed further and obtain the result as,

=a2maπ2ħ2sin3πxa-13sin5πxa+16sin7πxa

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Most popular questions from this chapter

Question: Sometimes it is possible to solve Equation 6.10 directly, without having to expand in terms of the unperturbed wave functions (Equation 6.11). Here are two particularly nice examples.

(a) Stark effect in the ground state of hydrogen.

(i) Find the first-order correction to the ground state of hydrogen in the presence of a uniform external electric fieldEext (the Stark effect-see Problem 6.36). Hint: Try a solution of the form

(A+Br+Cr2)e-r/acosθ

your problem is to find the constants , and C that solve Equation 6.10.

(ii) Use Equation to determine the second-order correction to the ground state energy (the first-order correction is zero, as you found in Problem 6.36(a)). Answer:-m(3a2eEext/2)2 .

(b) If the proton had an electric dipole moment p the potential energy of the electron in hydrogen would be perturbed in the amount

H'=-epcosθ4π̀o0r2

(i) Solve Equation 6.10 for the first-order correction to the ground state wave function.

(ii) Show that the total electric dipole moment of the atom is (surprisingly) zero, to this order.

(iii) Use Equation 6.14 to determine the second-order correction to the ground state energy. What is the first-order correction?

(a) Plugs=0,s=2, and s=3into Kramers' relation (Equation 6.104) to obtain formulas for (r-1),(r),(r-2),and(r3). Note that you could continue indefinitely, to find any positive power.

(b) In the other direction, however, you hit a snag. Put in s=-1, and show that all you get is a relation between role="math" localid="1658216018740" (r-2)and(r-3).

(c) But if you can get (r-2)by some other means, you can apply the Kramers' relation to obtain the rest of the negative powers. Use Equation 6.56(which is derived in Problem 6.33) to determine (r-3) , and check your answer against Equation 6.64.

Van der Waals interaction. Consider two atoms a distanceapart. Because they are electrically neutral you might suppose there would be no force between them, but if they are polarizable there is in fact a weak attraction. To model this system, picture each atom as an electron (mass m , charge -e ) attached by a spring (spring constant k ) to the nucleus (charge +e ), as in Figure. We'll assume the nuclei are heavy, and essentially motionless. The Hamiltonian for the unperturbed system is

H0=12mp12+12kx12+12mp22+12kx22[6.96]

The Coulomb interaction between the atoms is

H'=14πϵ0(e2R-e2R-x1-e2R+x2+e2R-x1+x2 [6.97]

(a) Explain Equation6.97. Assuming that localid="1658203563220" |x1| and |x2|are both much less than, show that

localid="1658203513972" H'-e2x1x22πϵ0R3 [6.98]

(b) Show that the total Hamiltonian (Equationplus Equation) separates into two harmonic oscillator Hamiltonians:

H=[12mp+2+12(k-e22πϵ0R3x+2]+[+12mp-2+12(k+e22πϵ0R3x-2] [6.99]

under the change of variables

x±12(x1±x2) Which entails p±=12(p1±p2) [6.100]

(c) The ground state energy for this Hamiltonian is evidently

E=12(ω++ω-) Where ω±=k(e2/2πϵ0R3)m [6.101]

Without the Coulomb interaction it would have been E0=ħω0, where ω0=k/m. Assuming that, show that

ΔVE-E0-8m2ω03(e22πϵ0)21R6. [6.102]

Conclusion: There is an attractive potential between the atoms, proportional to the inverse sixth power of their separation. This is the van der Waals interaction between two neutral atoms.

(d) Now do the same calculation using second-order perturbation theory. Hint: The unperturbed states are of the form ψn1(x1)ψn2(x2), where ψn(x)is a one-particle oscillator wave function with mass mand spring constant k;ΔVis the second-order correction to the ground state energy, for the perturbation in Equation 6.98 (notice that the first-order correction is zero).

Consider the (eight) n=2states, |2ljmj. Find the energy of each state, under weak-field Zeeman splitting, and construct a diagram like Figure 6.11 to show how the energies evolve asBext increases. Label each line clearly, and indicate its slope.

Question: The exact fine-structure formula for hydrogen (obtained from the Dirac equation without recourse to perturbation theory) is 16

Enj=mc2{1+an-j+12+j+122-a22-12-1}

Expand to order α4(noting that α1), and show that you recoverEquation .

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