/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Q40P Sometimes it is possible to solv... [FREE SOLUTION] | 91影视

91影视

Sometimes it is possible to solve Equation 6.10 directly, without having to expand 1nin 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 field (the Stark effect-see Problem 6.36). Hint: Try a solution of the form

(A+Br+Cr2)e-r/acos

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/2h)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'=-别辫肠辞蝉胃400r2~

(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?

Short Answer

Expert verified

(a) (i) The first -order correction to the ground state of hydrogen for the given condition is 11=-r(2a+r)cose(-r/a),=(meE"ext")/(22(a3).

(ii) The second-order correction for the given condition is E12=-m(3eE"ext"a2)2h2.

(b) (i) The first-order correction to the ground state wave function is

11=mep402a3cose-r/a

(ii) Total electric dipole moment of the atom vanishes.

(iii) The second-order correction to the ground state energyE12=43pea2E1

Step by step solution

01

Definition of the wave function of Hamiltonian function

In quantum physics, a wave function represents the quantum state of a particle as a function of spin, time, momentum, and location.

Additionally, it depends on the degrees of freedom that correspond to the broadest group of observables that can coexist.

02

(a) Determination of the first order correction

(i)

Consider equation 6.10.

H0-En0n1=-H-En1n0H0=-h22m2-e240r=-h22m2+2ar

鈥(颈)

Ground state, n=1, and for H'=eEextrcos , first-order correction to ground state energy E11 diminishes.

Now, the non-perturbed ground state energyE10=-h2/2ma2 and non-perturbed wave function for ground state of hydrogen is 10=e-r/a/a3 .

Calculate first-order correction to wave function.

11=A+Br+Cr2cose-r/a=frcose-r/a

Rearrange the equation (i).

-h22m2+2ar+h22ma211=-H'10211+2ar11-1a211=2mh2H'10

Write the operator in spherical coordinates.

211=1r2ddrr2ddrfrcose-r/a+1r2sinddsinddfrcose-r/a=cosr2ddrr2f'e-r/a-r2fae-r/a+fe-r/ar2sindd-sin2=cosr22rf'e-r/a+r2f"e-r/a--r2fae-r/a-r2fae-r/a-r2fae-r/a+r2fa2e-r/a-2rfe-r/ar2cos=cose-r/ar2r2f"+2rf'1-ra-f2+2ra-r2a2=cose-r/af"+2f1r-1a-f2r2+2ar-1a2

Use this equation.

cose-r/af"+2f'1r-1a-f2r2+2ar-1a2+2fcose-r/aar=2mh2eEextrcose-r/aa3

Perform the simplification.

f"+2f'1r-1a-fr2=rf(r)=A+Br+Cr22C+2(B=2Cr)1r-1a-2Ar2-2Ar-2C-r=0

Here,=2meEexth2a3,f'=B+2Cr,andf"=2C

Further simplify the above expression.

-2Ba+4C-4Cra-2Ar2-r=02Ar2-r=0A=04Cra-=0C=-a4=-meEext2h2a32Ba=-4CB=-ameEexth2

Write the first-order correction to wave function of ground state.

11=rB+Crcose-r/a=-r2a+rcose-r/a

Thus, the first-order correction to wave function of ground state is .

11==-r2a+rcose-r/a,and=meEext2h2a3

(ii)

Secondly find second-order correction of ground state energy, using equation 6.17.

E11=10H'11-O.1011=10H'11=e-r/aa3eEextrcos-r2a+rcose-r/ar2drsindd=-meEext2a2h20r4r+2ae-r/a0cos2sind

Further evaluate the expression.

E12=-meEext2a2h25!a26+2a4!a2523=-m3eEexta22h

Therefore, the second-order correction for the given condition is .

03

(b) Determination of the first order wave correction and the second order correction

Write the expression of Perturbation Hamiltonian.

H'=-epcos40r2cose-r/af"+2f'1r-1a-f2r2+2ar+1a2+2fcose-r/aar-fcose-r/aa3=2mh2-epcos40r2e-r/aa3f'+2f'1r-1a-2fr2=-2mep40h2a31r2f'+2f'1r-1a-2fr2=-2ar2fr==2mep40h2a3

Write the first-order correction to wave function of ground state energy.

=11mep40h2a3cose-r/a

Write the expression for the electric dipole.

pe=-ercos=-e10+11rcos10+11=10rcos10+210rcos11+11rcos11

Write the third order of the term.

pe=-210rcos11=-2ee-r/aa3rcoscos-r/ar2drsindd=-4ea30r3e-2/adr0cos2sind=-4ea33!a2423=-me2a40h2p=-p

Write the expressions for second-order correction to the ground state energy.

E12=10H11=e-r/aa3-epcos40r2cose-r/ar2drsindd=-2mep2402h2a223=43-me42402h2p2e2a2=43pea2E1

(i) Thus, the first-order correction to the ground state wave function is

11=mep402(a3cose-r/a

(ii) Thus, the total electric dipole moment of the atom vanishes.

(iii) Thus, the second-order correction to the ground state energy isE12=43pea2E1

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with 91影视!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

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/acos

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'=-epcos4o0r2

(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?

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'=14蟺系0(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'-e2x1x220R3 [6.98]

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

H=[12mp+2+12(k-e220R3x+2]+[+12mp-2+12(k+e220R3x-2] [6.99]

under the change of variables

x12(x1x2) Which entails p=12(p1p2) [6.100]

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

E=12(++-) Where =k(e2/20R3)m [6.101]

Without the Coulomb interaction it would have been E0=0, where 0=k/m. Assuming that, show that

VE-E0-8m203(e220)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 n1(x1)n2(x2), where n(x)is a one-particle oscillator wave function with mass mand spring constant k;Vis the second-order correction to the ground state energy, for the perturbation in Equation 6.98 (notice that the first-order correction is zero).

Use Equation 6.59 to estimate the internal field in hydrogen, and characterize quantitatively a "strong" and "weak" Zeeman field.

Starting with Equation 6.80, and using Equations 6.57, 6.61, 6.64, and 6.81, derive Equation 6.82.

Consider a charged particle in the one-dimensional harmonic oscillator potential. Suppose we turn on a weak electric field (E), so that the potential energy is shifted by an amountH'=-qEx.(a) Show that there is no first-order change in the energy levels, and calculate the second-order correction. Hint: See Problem 3.33.

(b) The Schr枚dinger equation can be solved directly in this case, by a change of variablesx'x-(qE/m蝇2). Find the exact energies, and show that they are consistent with the perturbation theory approximation.

See all solutions

Recommended explanations on Physics Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.