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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 Schr枚dinger equation can be solved directly in this case, by a change of variablesx'x-(qE/尘蝇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=魔蝇n+12-q2E22尘蝇2

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=2尘蝇(a++a-)

Next, calculate the n-th diagonal matrix element:

n>=2尘蝇na++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=-qE2尘蝇a++a-

Proceed by doing calculation of the following matrix elements:

iHej=-qE2尘蝇ia++a-j=-qE2尘蝇ia+j+ia-j=-qE2尘蝇ij+1j+1+ijj-1=-qE2尘蝇j+1i,j+1+箩未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=qE2尘蝇j2Ej-10-Ej0+qE2尘蝇j+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 to. Therefore, the terms in the denominators are easily evalued leading to:

Ej2=q2E2魔蝇2尘蝇-j+1+jEj2=q2E22尘蝇

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/尘蝇2x=x+qE/尘蝇2

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

-2m2x2x+12尘蝇2x2x-辩贰虫蠄x=贰蠄x-22m2x'2x+12尘蝇2x+qE/尘蝇22x-qEx+qE/尘蝇2x=贰蠄x

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

-22m2x'2x'+12尘蝇2x'2+2x'qE/尘蝇2+q2E2/m24-qEx'b+qE/尘蝇2x=贰蠄x'

see that many terms cancel out, leaving this:

-22m2x'2x'+12尘蝇2x'2=E+q2E2/2尘蝇2x

By defination E'E+q2E2/2尘蝇2the Schrodinger equation reads:

-2m2x2x'+12尘蝇2x'2=E'x

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:

魔蝇n+12=E+q2E2/2m2E=魔蝇n+12-q2E22尘蝇2

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

Van der Waals interaction. Consider two atoms a distanceapart. Because they are electrically neutral you might suppose there would be no force between them, but if they are polarizable there is in fact a weak attraction. To model this system, picture each atom as an electron (mass m , charge -e ) attached by a spring (spring constant k ) to the nucleus (charge +e ), as in Figure. We'll assume the nuclei are heavy, and essentially motionless. The Hamiltonian for the unperturbed system is

H0=12mp12+12kx12+12mp22+12kx22[6.96]

The Coulomb interaction between the atoms is

H'=14蟺系0(e2R-e2R-x1-e2R+x2+e2R-x1+x2 [6.97]

(a) Explain Equation6.97. Assuming that localid="1658203563220" |x1| and |x2|are both much less than, show that

localid="1658203513972" H'-e2x1x220R3 [6.98]

(b) Show that the total Hamiltonian (Equationplus Equation) separates into two harmonic oscillator Hamiltonians:

H=[12mp+2+12(k-e220R3x+2]+[+12mp-2+12(k+e220R3x-2] [6.99]

under the change of variables

x12(x1x2) Which entails p=12(p1p2) [6.100]

(c) The ground state energy for this Hamiltonian is evidently

E=12(++-) Where =k(e2/20R3)m [6.101]

Without the Coulomb interaction it would have been E0=0, where 0=k/m. Assuming that, show that

VE-E0-8m203(e220)21R6. [6.102]

Conclusion: There is an attractive potential between the atoms, proportional to the inverse sixth power of their separation. This is the van der Waals interaction between two neutral atoms.

(d) Now do the same calculation using second-order perturbation theory. Hint: The unperturbed states are of the form n1(x1)n2(x2), where n(x)is a one-particle oscillator wave function with mass mand spring constant k;Vis the second-order correction to the ground state energy, for the perturbation in Equation 6.98 (notice that the first-order correction is zero).

Consider the isotropic three-dimensional harmonic oscillator (Problem 4.38). Discuss the effect (in first order) of the perturbation H'=位虫2yz

(for some constant ) on

(a) the ground state

(b) the (triply degenerate) first excited state. Hint: Use the answers to Problems 2.12and 3.33

Starting with Equation 6.80, and using Equations 6.57, 6.61, 6.64, and 6.81, derive Equation 6.82.

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.

Use Equation 6.59 to estimate the internal field in hydrogen, and characterize quantitatively a "strong" and "weak" Zeeman field.

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