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

Short Answer

Expert verified

To calculate energy corrections, one needs to find matrix elements (or expectation values) of the perturbation Hamiltonian in an unperturbed basis.

First order correction =0

Second order correctionE=ħωn+12-q2E222

Step by step solution

01

Prove that the diagonal matrix element vanishes for every eigen state of the quantum harmonic oscillator.

a)

See how the interaction Hamiltonian includes the position operator:

He=-qEx, prove that the diagonal matrix element (or equivalently expectation value of the position operator) vanishes for every eigen state of the quantum harmonic oscillator. Express the position operator in the terms of raising and lowering operators:x=ħ2(a++a-)

Next, calculate the n-th diagonal matrix element:

n>=ħ2na++a-n=0En1=0

The latter is equal to zero because the lowering operator turns n~n-1and raising operator turnsn~n+1, so the both inner products vanish since the different eigen states are mutually orthogonal. Therefore, there are no corrections of the first order in the energy levels.

Second order corrections are calculated by the useof the following relation:

Ej2=i=jiHej2Ei0-Ej0

Where Ek0denote the unperturbed energy levels - energy levels of the harmonic oscillator. Start by expressing the interaction Hamiltonian in the terms of raising and lowering operators:

Hi=-qEħ2a++a-

Proceed by doing calculation of the following matrix elements:

iHej=-qEħ2ia++a-j=-qEħ2ia+j+ia-j=-qEħ2ij+1j+1+ijj-1=-qEħ2j+1δi,j+1+i,j-1

02

Second order correction.

See that the only non-vanishing matrix elements are the ones neighbouring j-th element. Therefore, the sum in equation (1) is simplified, having only two contributing terms:

Ej2=qEħ2j2Ej-10-Ej0+qEħ2j+12Ej+10-Ej0

Since problem is dealing with the energy spectrum of the harmonic oscillator, the unperturbed energies are equidistant the distance between two increasing levels is equal toħω. Therefore, the terms in the denominators are easily evalued leading to:

Ej2=q2E2ħωħ2-j+1+jEj2=q2E22

What is interesting is that the energy corrections of the second order do not depend on the energy level jthat we are observing - all levels are corrected by the same amount. This is exactly the reason that would lead one to think that there might be an analytical method of obtaining the energy spectrum by manipulating the original Hamiltonian and attempting to solve it in a non-perturbative manner.

03

Solve the Schrödinger equation and find the exact energies.

b)

To solve the Schrodinger analytically, begin by the use of the following substitution:

x˙=x-qE/2x=x˙+qE/2

Next step is to insert this substitution into the original Schrodinger equation:

-ħ2m2x2ψx+122x2ψx-qExψx=x-ħ22m2x'2ψx˙+122x˙+qE/22ψx˙-qEx˙+qE/2ωx=x˙

It is important to notice that the change in derivative yields no extra factors, sincex˙x=1. Squaring the term in the brackets, obtain the following:

-ħ22m2x'2ψx'+122x'2+2x'qE/2+q2E2/m2ω4-qEx'b+qE/2ψx=x'

see that many terms cancel out, leaving this:

-ħ22m2x'2ψx'+122x'2=E+q2E2/22ψx˙

By defination E'E+q2E2/22the Schrodinger equation reads:

-ħ2m2x2ψx'+122x'2=E'ψx

Which is simply an equation of a quantum harmonic oscillator, with known solutions. Therefore, the energies of the original problem,E, are given by a simple relation:

ħωn+12=E+q2E2/2m2E=ħωn+12-q2E222

This is exactly the same result that is obtained by calculating the energy corrections of the second order. This implies that perturbative method actually provided the exact solution. This is usually not the case - usually one would have to calculate infinite corrections to approach the exact value.

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Most popular questions from this chapter

Work out the matrix elements of HZ'andHfs'construct the W matrix given in the text, for n = 2.

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).

Let aand bbe two constant vectors. Show that

(a.r)(b.r)sinθdθdϕ=4π3(a.b)

(the integration is over the usual range:0<θ<π,0<ϕ<2π). Use this result to demonstrate that

(3Sp.rSe.r-Sp.Ser3)=0

For states with I=0. Hint:r=sinθcosϕi+sinθsinϕΦ+cosθk.

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

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?

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