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

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.

Short Answer

Expert verified

The answers are

a)v1=100,V0;v2=010,V0;v3=001,2V0

b)role="math" localid="1658144006650" λ1=V0(1-o˙),λ2=V023-4o˙2V0(1-o˙2),λ3=V023+4o˙2V0(2-o˙2)

c)E31=0,E32,=o˙2V0

d)E1=V0-o˙V0,E2=V01+

Step by step solution

01

Cigen vector and eigen values of Hamiltonian

a)

In this problem we study the Hamiltonian

H=V01-o˙0000o˙0o˙2

The unperturbed Hamiltonian is obtained by settingo˙=0 and is of the form

Since it is diagonal, its Eigen values are

V0,V0,2V0

And

the eigenvectors are

V1=100V2=010V3=001

02

Expand eigen values as power series of H

b)

We now diagonalize the total Hamiltonian by solving the equation

V0(1-o˙)-λ000V0-λV0o˙0V0o˙2V0-λ=0(V0(1-o˙)-λ)(V0-λ)(2V0-λ)-V02o˙2(V0(1-o˙)-λ)=0(V0(1-o˙)-λ)(V0-λ)(2V0-λ)-V02o˙2=0

The one eigen value is

λ1=V0(1-o˙)

and the other two are obtained as

λ2-3V0λ+V0(2-o˙2)=0λ2,3=123V0±9V02-4V02(2-o˙2)=V023±1+4o˙2

We can expand these Eigen values with respect to to obtain

λ1=V0(1-o˙),λ2=V023+1+4o˙2V02(3+1+2o˙2)=V02+o˙2λ3=V023-1+4o˙2V02(3-1-2o˙2)=V01-o˙2

We have used the Taylor expansion of the square root 1+o˙1+o˙/2.

03

Find approximate eigen values for state

c)

We now observe the perturbed part of the Hamiltonian

H=o˙V0-100001010

By settingo˙=0we see that λ1=λ2, so we are calculating the corrections for E3. The first-order correction is

The second-order corrections are

E32=m-12vmHv32E30-Em0

We have

localid="1658203255352" vmHv3=o˙V0(100)-100001010001=0vmHv3=o˙V0(010)-100001010001=o˙V0E30-E20=2V0-V0=V0

Therefore,

Ea2=o˙V02V0=o˙2V0

The total energy is then

E3=E30+E31+E32=2V0+0+o˙2V0=V02+o˙2

which is what we obtained by expanding the exact solution.

04

First order eigen values for degenerate state

d)

We now calculate the corrections to the degenerate energies. We have

Waa=v1Hv1=o˙V0(100)-100001010100=-o˙V0Wbb=v2Hv2=o˙V0(010)-100001010010=0Wab=v1Hv2=o˙V0(100)-100001010010=0E30-E20=2V0-V0=V0

The energies are

E±1=12Waa+Wbb±Waa-Wbb2+4Wab2=12Waa±Waa=12-o˙Va±o˙V0

The energies corrections are

E-=-o˙V0,E+=0

and the energies are

E1=V0-o˙V0,E2=V0

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

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.

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.

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.

Analyze the Zeeman effect for the n=3states of hydrogen, in the weak, strong, and intermediate field regimes. Construct a table of energies (analogous to Table 6.2), plot them as functions of the external field (as in Figure 6.12), and check that the intermediate-field results reduce properly in the two limiting cases.

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

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