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

Question: Consider a quantum system with just three linearly independent states. Suppose the Hamiltonian, in matrix form, is

H=V0(1-o˙0000o˙0o˙2)

WhereV0is a constant, ando˙is some small number(1).

(a) Write down the eigenvectors and eigenvalues of the unperturbed Hamiltonian(o˙=0).

(b) Solve for the exact eigen values of H. Expand each of them as a power series ino˙, up to second order.

(c) Use first- and second-order non degenerate perturbation theory to find the approximate eigen value for the state that grows out of the non-degenerate eigenvector ofH0. Compare the exact result, from (a).

(d) Use degenerate perturbation theory to find the first-order correction to the two initially degenerate eigen values. Compare the exact results.

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.

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?

Question: Consider the Stark effect (Problem 6.36) for the states of hydrogen. There are initially nine degenerate states, ψ3/m (neglecting spin, as before), and we turn on an electric field in the direction.

(a) Construct the matrix representing the perturbing Hamiltonian. Partial answer: <300|z|310>=-36a,<310|z|320>=-33a,<31±1|z|32±1>=-(9/2)a,,

(b) Find the eigenvalues, and their degeneracies.

Consider a particle of mass m that is free to move in a one-dimensional region of length L that closes on itself (for instance, a bead that slides frictionlessly on a circular wire of circumference L, as inProblem 2.46).

(a) Show that the stationary states can be written in the formψn(x)=1Le2πinx/L,(-L/2<x<L/2),

wheren=0,±1,±2,....and the allowed energies areEn=2mnπL2.Notice that with the exception of the ground state (n = 0 ) – are all doubly degenerate.

(b) Now suppose we introduce the perturbation,H'=-V0e-x2/a2where aLa. (This puts a little “dimple” in the potential at x = 0, as though we bent the wire slightly to make a “trap”.) Find the first-order correction to En, using Equation 6.27. Hint: To evaluate the integrals, exploit the fact that aLato extend the limits from ±L/2to±after all, H′ is essentially zero outside -a<x<a.

E±1=12Waa+Wbb±Waa-Wbb2+4Wab2(6.27).

(c) What are the “good” linear combinations ofψnandψ-n, for this problem? Show that with these states you get the first-order correction using Equation 6.9.

En'=ψn0H'ψn0(6.9).

(d) Find a hermitian operator A that fits the requirements of the theorem, and show that the simultaneous Eigenstates ofH0and A are precisely the ones you used in (c).

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