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To determine the two bound state energies for the well.

Short Answer

Expert verified

The two bound state energies for a well is E1=7.2822mL2 and E2=27.9h22mL2.

Step by step solution

01

formula used to determine the two bound state energies for the well.

Given Information:

U0=4π222mL2

Formula Used:

The result of the exercise 40 is

Ecot2mEhL=U0E

Here, E is the energy,m is the mass, h is the reduced Planck's constant, L is the width of the infinite well and U0 is the potential energy of the particle.

02

Calculating the two bound state energies using the formula 

Multiply the above equation by 2mEhL on both sides

This modifies the equation to:

2mhLEcot2mEhL=2mhL(U0E)2mEhLcot2mEhL=2mU0L22mEL2h2

Make the substitution,x=2mEhL

xcot(x)=2mU0L22x2 …… (1)

The potential energyU0 is

U0=4π222mL2

Substitute the above equation in the equation (1) and simplify.

xcot(x)=2m4π2h22mL2L2h2x2xcot(x)=4π2x2

This is a very nice function to plug into computer program of choice.

Solutions are:

x=2.698and5.284Forx=2.6982.698=2mE1hLE12.6982=hh2mL2=7.28h22mL2

And forx=5.284we get

5.284=2mE2hLE25.2842=h2mL2=27.9h22mL2

Hence, the two bound state energies for a well is E1=7.28h22mL2 and E2=27.9h22mL2.

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Most popular questions from this chapter

The potential energy shared by two atoms in a diatomic molecule, depicted in Figure 17, is often approximated by the fairly simple function U(x)=(ax12)-(bx6)where constants a and b depend on the atoms involved. In Section 7, it is said that near its minimum value, it can be approximated by an even simpler function—it should “look like” a parabola. (a) In terms ofa and b, find the minimum potential energy U (x0) and the separation x0 at which it occurs. (b) The parabolic approximation UP(x)=U(xo)+12κ(x-xo)2has the same minimum value at x0 and the same first derivative there (i.e., 0). Its second derivative is k , the spring constant of this Hooke’s law potential energy. In terms of a and b, what is the spring constant of U (x)?

In the harmonic oscillators eave functions of figure there is variation in wavelength from the middle of the extremes of the classically allowed region, most noticeable in the higher-n functions. Why does it vary as it does?

Consider the delta well potential energy:

U(x)={0x0-x=0

Although not completely realistic, this potential energy is often a convenient approximation to a verystrong, verynarrow attractive potential energy well. It has only one allowed bound-state wave function, and because the top of the well is defined as U = 0, the corresponding bound-state energy is negative. Call its value -E0.

(a) Applying the usual arguments and required continuity conditions (need it be smooth?), show that the wave function is given by

ψ(x)=(2mE0h2)1/4e-(2mE0/)|x|

(b) Sketch ψ(x)and U(x) on the same diagram. Does this wave function exhibit the expected behavior in the classically forbidden region?

Quantization is an important characteristic of systems in which a particle is bound in a small region. Why "small," and why "bound"?

Using equation (23), find the energy of a particle confined to a finite well whose walls are half the height of the ground-state infinite well energy, . (A calculator or computer able to solve equations numerically may be used, but this happens to be a case where an exact answer can be deduced without too much trouble.)

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