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When an atom is placed in a uniform external electric field ,the energy levels are shifted-a phenomenon known as the Stark effect (it is the electrical analog to the Zeeman effect). In this problem we analyse the Stark effect for the n=1 and n=2 states of hydrogen. Let the field point in the z direction, so the potential energy of the electron is

H's=eEextz=eEextrcosθ

Treat this as a perturbation on the Bohr Hamiltonian (Equation 6.42). (Spin is irrelevant to this problem, so ignore it, and neglect the fine structure.)

(a) Show that the ground state energy is not affected by this perturbation, in first order.

(b) The first excited state is 4-fold degenerate: Y200,Y211,Y210,Y200,Y21-1Using degenerate perturbation theory, determine the first order corrections to the energy. Into how many levels does E2 split?

(c) What are the "good" wave functions for part (b)? Find the expectation value of the electric dipole moment (pe=-er) in each of these "good" states.Notice that the results are independent of the applied field-evidently hydrogen in its first excited state can carry a permanent electric dipole moment.

Short Answer

Expert verified

(a)ES1=0(b)E2,E2,E2+3aeEextE2-3aeEext(c)TheEigenvectors:ψ211'ψ21-112(ψ200+ψ210)$.Expectationvalues:pe-0pe-0pe-+3eaz^

Step by step solution

01

Define the formula for wave function in ground state

Wave function of ground state in hydrogen is: ψ100=e-r/aπa3

Correction in ground state E11=<ψ100|HS|ψ100>

02

Effect of perturbation on ground state energy

100>=1πa3e-r/a...(4.80)E1S=100H'100eEext1πa3e-2r/a(rcosθ)r2sinθdrdθdϕButtheθintegraliszero:0πcosθsinθdθ=sin2θ0πSo,=0E1S=0

03

first order corrections to the energy

From problem 4.11:1>=ψ200=12πa212a1-r2ae-2/2a2>=ψ211=1πa18a2re-r/2asinθeiϕ3>=ψ210=12πa14are-r/2acosθ4>=ψ21-1=1πa18a2re-r/2asinθeiϕ

1H's1=...0πcosθsinθdθ=02H's2=...0πsin2θcosθsinθdθ=03H's3=...0πcos2θsinθdθ=04H's4=...0πsin2θcosθsinθdθ=01H'S2=...02πeiϕdϕ=01H'S4=...02πeiϕdϕ=02H'S3=...02πeiϕdϕ=02H'S4=...02πeiϕdϕ=02H'S4=...02πeiϕdϕ=0

All matrix elements of are zero except 1H'S3and3H'S1 (which are complex conjugates, so only needs to be evaluated).
role="math" localid="1658313451117" 1H'S3=eEext12πa12a12πa14a21-r2ae-r/2acosθ(rcosθ)r2sinθdrdθdϕ=1H'S3=eEext12πa12a12πa14a21-r2ae-r/2acosθ(rcosθ)r2sinθdrdθdϕ=eEext2πa8a3(2π)0πcos2θsinθdθ01-r2ae-r/ar4dr=eEext8a4230r4e-r/adr-12a0r5e-r/adr=eEext8a44!a5-12a5!a6=eEext8a424a5(1-52)=eaEext(-3)=-3aeEextW=-3aeEext0010000010000000

There is need of eigenvalues of this matrix. The characteristic equation is:

-λ0100-λ0010-λ0000-λ=-λ-λ000-λ000-λ+0-λ010000-λ=-λ(-λ)3+(-λ2)=λ2(λ2-10=0

So, The eigenvalues are 0,01, and -1 , so the perturbed energies are

E2,E2,E2+3aeEext,E2-3aeEext

04

Obtain the electric dipole operator.

On the basis of Eigen vectors

pe=-er=-er(sinϑcosφx^+sinϑsinφy^+cosϑz^)

pe4=ψ(21-1)*peψ(21-1)d3r=-e1πa18a2r2e-r/asin2ϑe-iφ+iφr(sinϑcosφx^+sinϑsinφy^+cosϑz)^=002πsinφdφ=02πcosφdφ=0and0πsin3ϑcosϑdϑ=0As=pe2=0pe2=-e2(ψ200+ψ210)2r((sinϑcosφx^+sinϑsinφy^+cosϑz)^r2drsinϑdϑdφNowitegtrate02πsinϑdφ=02πcosφdφ=0

Here we have only Z-component

pe2=-eπz^(ψ2200+2ψ200+ψ210+ψ2+ψ2210)r3drsinϑdϑ=-eπz^12πa14a21-r2a2e-r/a+212πa18a31-r2are-r/acosϑ+12πa116a4r2e-r/acos2ϑr3drsinϑdϑsinϑcosϑdϑ=0andsinϑcos3ϑdϑ=0pe±=eπz^18a401-r2ar4e-r/adr0πcos2ϑsinϑdϑ=+ez8a423a5.4!-12aa65!pe±=±3eaz^

Thus the Eigenvectors: ψ_211,ψ_(21-1),1/2(ψ_200+ψ_210),1/2(ψ_200-ψ_210)$.

Expectation values:

pe2=0pe4=0pe=±3eaz^

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Most popular questions from this chapter

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 .

Suppose the Hamiltonian H, for a particular quantum system, is a function of some parameter λlet En(λ)and ψn(λ)be the eigen values and

Eigen functions of. The Feynman-Hellmann theorem22states that

Enλ=(ψnHλψn)

(Assuming either that Enis nondegenerate, or-if degenerate-that the ψn's are the "good" linear combinations of the degenerate Eigen functions).

(a) Prove the Feynman-Hellmann theorem. Hint: Use Equation 6.9.

(b) Apply it to the one-dimensional harmonic oscillator,(i)using λ=ω(this yields a formula for the expectation value of V), (II)using λ=ħ(this yields (T)),and (iii)using λ=m(this yields a relation between (T)and (V)). Compare your answers to Problem 2.12, and the virial theorem predictions (Problem 3.31).

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?

(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.

Question: In a crystal, the electric field of neighbouring ions perturbs the energy levels of an atom. As a crude model, imagine that a hydrogen atom is surrounded by three pairs of point charges, as shown in Figure 6.15. (Spin is irrelevant to this problem, so ignore it.)

(a) Assuming that rd1,rd2,rd3show that

H'=V0+3(β1x2+β2y2+β3z2)-(β1+β2+β3)r2

where

βi-e4πε0qidi3,andV0=2(β1d12+β2d22+β3d32)

(b) Find the lowest-order correction to the ground state energy.

(c) Calculate the first-order corrections to the energy of the first excited states Into how many levels does this four-fold degenerate system split,

(i) in the case of cubic symmetryβ1=β2=β3;, (ii) in the case of tetragonal symmetryβ1=β2β3;, (iii) in the general case of orthorhombic symmetry (all three different)?

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