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

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Most popular questions from this chapter

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.

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.

For the harmonic oscillator[Vx=1/2kx2], the allowed energies areEN=(n+1/2)ħω,(n=0.1.2,..),whererole="math" localid="1656044150836" ω=k/mis the classical frequency. Now suppose the spring constant increases slightly:k(1+ο')k(Perhaps we cool the spring, so it becomes less flexible.)

(a) Find the exact new energies (trivial, in this case). Expand your formula as a power series inο,, up to second order.

(b) Now calculate the first-order perturbation in the energy, using Equation 6.9. What ishere? Compare your result with part (a).

Hint: It is not necessary - in fact, it is not permitted - to calculate a single integral in doing this problem.

Estimate the correction to the ground state energy of hydrogen due to the finite size of the nucleus. Treat the proton as a uniformly charged spherical shell of radius b, so the potential energy of an electron inside the shell is constant:-e2/(4πϵ0b);this isn't very realistic, but it is the simplest model, and it will give us the right order of magnitude. Expand your result in powers of the small parameter, (b / a) whereis the Bohr radius, and keep only the leading term, so your final answer takes the form ΔEE=A(b/a)n. Your business is to determine the constant Aand the power n. Finally, put in b10-15m(roughly the radius of the proton) and work out the actual number. How does it compare with fine structure and hyperfine structure?

Consider the (eight) n=2states,|2lmlms.Find the energy of each state, under strong-field Zeeman splitting. Express each answer as the sum of three terms: the Bohr energy, the fine-structure (proportional toa2), and the Zeeman contribution (proportional toμBBext.). If you ignore fine structure altogether, how many distinct levels are there, and what are their degeneracies?

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