Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

Sometimes it is possible to solve Equation 6.10 directly, without having to expand ψ1nin 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/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/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'=-epcosθ4π00r2~

(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 ψ11=-βr(2a+r)cosϑe(-r/a),β=(meE"ext")/(22(πa3).

(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

ψ11=mep4πε02πa3cosϑe-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-En0ψn1=-H-En1ψn0H0=-h22m2-e24πε0r=-h22m2+2ar

…(i)

Ground state, n=1, and for H'=eEextrcosθ , 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 ψ10=e-r/a/πa3 .

Calculate first-order correction to wave function.

ψ11=A+Br+Cr2cosθe-r/a=frcosθe-r/a

Rearrange the equation (i).

-h22m2+2ar+h22ma2ψ11=-H'ψ102ψ11+2arψ11-1a2ψ11=2mh2H'ψ10

Write the operator in spherical coordinates.

2ψ11=1r2ddrr2ddrfrcosθe-r/a+1r2sinθddθsinθddθfrcosθe-r/a=cosθr2ddrr2f'e-r/a-r2fae-r/a+fe-r/ar2sinθddθ-sin2θ=cosθr22rf'e-r/a+r2f"e-r/a--r2fae-r/a-r2fae-r/a-r2fae-r/a+r2fa2e-r/a-2rfe-r/ar2cosθ=cosθe-r/ar2r2f"+2rf'1-ra-f2+2ra-r2a2=cosθe-r/af"+2f1r-1a-f2r2+2ar-1a2

Use this equation.

cosθe-r/af"+2f'1r-1a-f2r2+2ar-1a2+2fcosθe-r/aar=2mh2eEextrcosθe-r/aπa3

Perform the simplification.

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

Here,λ=2meEexth2πa3,f'=B+2Cr,andf"=2C

Further simplify the above expression.

-2Ba+4C-4Cra-2Ar2-λr=02Ar2-λr=0A=04Cra-λ=0C=-aλ4=-meEext2h2πa32Ba=-4CB=-aπmeEexth2

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

ψ11=rB+Crcosθe-r/a=-βr2a+rcosθe-r/a

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

ψ11==-βr2a+rcosθe-r/a,andβ=meEext2h2πa3

(ii)

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

E11=ψ10H'ψ11-O.ψ10ψ11=ψ10H'ψ11=e-r/aπa3eEextrcosθ-βr2a+rcosθe-r/ar2drsinθdθdφ=-meEext2a2h20r4r+2ae-r/a0πcos2θsinθdθ

Further evaluate the expression.

E12=-meEext2a2h25!a26+2a·4!a25·23=-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'=-epcosθ4πε0r2cosθe-r/af"+2f'1r-1a-f2r2+2ar+1a2+2fcosθe-r/aar-fcosθe-r/aa3=2mh2-epcosθ4πε0r2e-r/aπa3f'+2f'1r-1a-2fr2=-2mep4πε0h2πa31r2f'+2f'1r-1a-2fr2=-2ar2fr=α=2mep4πε0h2πa3

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

=ψ11mep4πε0h2πa3cosθe-r/a

Write the expression for the electric dipole.

pe=-ercosθ=-eψ10+ψ11rcosθψ10+ψ11=ψ10rcosθψ10+2ψ10rcosθψ11+ψ11rcosθψ11

Write the third order of the term.

pe=-2ψ10rcosθψ11=-2ee-r/aπa3rcosθαcosϑ-r/ar2drsinθdθdφ=-4πeαπa30r3e-2/adr0πcos2θsinθdθ=-4πeαπa3·3!a24·23=-me2a4πε0h2·p=-p

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

E12=ψ10Hψ11=e-r/aπa3-epcosθ4πε0r2αcosθe-r/ar2drsinθdθdφ=-2mep24πε02h2·a2·23=43-me424πε02h2p2e2a2=43pea2E1

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

ψ11=mep4πε02(πa3cosϑe-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 Vaia!

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

The Feynman-Hellmann theorem (Problem 6.32) can be used to determine the expectation values of1/rand1/r2for hydrogen.23The effective Hamiltonian for the radial wave functions is (Equation4.53)

22md2dr2+22ml(l+1)r2-e24π01r

And the eigenvalues (expressed in terms ofl)24are (Equation 4.70)

En=-me432π202h2jmax+l+12

(a) Use λ=ein the Feynman-Hellmann theorem to obtain 1/r. Check your result against Equation 6.55.

(b) Use λ=lto obtain 1/r2. Check your answer with Equation6.56.

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.

Prove Kramers' relation:

sn2rs-(2s+1)ars-1+s4[(2l+1)2-s2]a2rs-2=0

Which relates the expectation values of rto three different powers (s,s-1,ands-2),for an electron in the state ψn/mof hydrogen. Hint: Rewrite the radial equation (Equation) in the form

u''=[l(l+1)r2-2ar+1n2a2]u

And use it to expressrole="math" localid="1658192415441" (ursu'')drin terms of (rs),(rs-1)and(rs-2). Then use integration by parts to reduce the second derivative. Show that (ursu'')dr=-(s/2)(rs-1)and(u'rsu')dr=-[2/s+1](u''rs+1u')dr. Take it from there.

Question: Use the virial theorem (Problem 4.40) to prove Equation 6.55.

Consider the isotropic three-dimensional harmonic oscillator (Problem 4.38). Discuss the effect (in first order) of the perturbation H'=λx2yz

(for some constant λ) on

(a) the ground state

(b) the (triply degenerate) first excited state. Hint: Use the answers to Problems 2.12and 3.33

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.

Sign-up for free