(a) Use a trial wave function of the form

ψ(x)={Acos(πx/a),if(a/2<x<a/2)0otherwise

to obtain a bound on the ground state energy of the one-dimensional harmonic oscillator. What is the "best" value ofa? CompareHminwith the exact energy. Note: This trial function has a "kink" in it (a discontinuous derivative) at±a/2; do you need to take account of this, as I did in Example 7.3?

(b) Useψ(x)=Bsin(πx/a)on the interval(a,a)to obtain a bound on the first excited state. Compare the exact answer.

Short Answer

Expert verified

(a) The exact energy is 12ωandHmin>Eg .

(b) The first actual excited state energy is 32ωHmin>32ω.

Step by step solution

01

Step 1:Definition ofthe Hamiltonian function

The Hamiltonian function is a mathematical formulation for describing the rate of change in the state of a dynamic physical system, such as a group of moving particles, The Hamiltonian of a system reveals all of its potential for generating energy.

02

(a) Determination of the expectation value of the potential energy

Write the normalization condition.

|ψ(x)|2dx=1|A|2a/2π/2cos2(πx/a)dx=1|A|2a/2a/2[1+cos2(πx2)2]dx=1|A|2[0a/2dx+0a/2cos(2πxa)dx]=1|A|2[x+sin(2πxa)(2πa)]0a/2

Evaluate the above expression further.

|ψ(x)|2dx=1|A|2[a2+0]=1A=2a

It is known thatH=T+Vand for a harmonic oscillator,T=22md2dx2andV=12mω2x2.

Determine the expectation value of.T

T=ψ*(x)(22md2dx2)ψ(x)dx=22m|A|2cos(πxa)ddx(sin(πxa))(πa)dx=22m|A|2(π2a2)a/2a/2cos2(πxa)dx=(22m)(π2a2)α/2α/2|ψ|2dx=(22m)(π2a2)(1)=(22m)(π2a2)

Determine the expectation value of V.

V=12mω2A2a2a2x2cos2πxadx=a2a2x2cos2πxadx=a2a2x22(1+cos2πxa)dx=a2a2x22dx+12a2a2x2cos2πxadx=I1+I2

Simplify the above expression further.

I1=x36|a2a2=a38×6(a38×6)=a348+a348=a324

I2=12a2a2x2cos2πxadx

Integrate the function by parts,

Assume u=x2,dv=cos2πxadx and du=2xdx.

v=sin2πxa2πa=asin2πxa2π

I2=ax2sin2πxa2π|a2a2aπa2a2xsin2πxadx=ax2sin2πxa2π|a2a2aπa2a2xsin2πxadx

Further simplify,

Assume u=x,dv=sin2πxadx,du=dx

v=a2πcos2πxa

Simplify the expression.

I2=ax2sin2πxa2πaπ(a2πxcos2πxaa2a2a2πcos2πxadx)=ax22πsin(2πxa)|a2a2+a22π2xcos2πxa|a2a2a22π2a2πsin2πxa=a22π2xcos(2πxa)|a2a2=a22π2(a2)(1)a22π2(a2)(1)

Further evaluate the expression.

I2=a34π2a34π2=12(a32π2)=a34π2

Write the value of l.

I=12mω2(2a)(a324a34π2)

Determine the expectation value of the Hamiltonian by substituting the values in.

H=T+V

Take the derivative of above expression with respect to a.

dHda=π22ma3+mω2aaπ2(π261)

Equate the above expression to 0.

dHda=0π22ma3+mω2aaπ2(π261)=0=mω2a2π2(π261)=π22ma3

Solve to get the value of a.

a=πmω(2(π261))14a4=aπ2π22mω2(π261)m=2π42m2ω2(π261)a=πmω(2(π261))14

Substitute the above value in the expression forH.

T=(22m)(π2a2)(1)=(22m)(π2a2)=ω2π2612+w42π261=12ωπ232=12ω(1.136)=12ω

Thus, the exact energyis 12ωand .Hmin>Eg

03

(b) Determination of a bound on the first excited state

Write the expression for the wave function.

ψ(x)=Bsin(πx/a)

Determine the normalization condition.

|ψ(x)|2dx=1|B|2aasin2(πxa)=1|B|2aa1cos(2πxa)2=1|B|22a(1cos2πxa)dx=1

Evaluate the above expression further.

|B|22[(x)aa(sin2πxa)|a(2πa)|a]=1|B|2a=1B=1a

Determine the bound to the energy of the first excited state since the given state is orthogonal to the ground state.

It is known thatH=T+V.

Determine the value ofT.

T=(22m)ψ(x)d2dx2ψ(x)dx=(22m)|B|2sin(πxa)[(πa)2sin(πxa)]dx=(22m)((πa)2)|B|2aasin2(πxa)dx=(22m)(π2a2)(1a)(a)=π222ma2

Determine the value ofV.

V=ψ(x)(12mω2x2)ψ(x)dx=|B|2(12)mω2θax2sin2(πxa)dx

Applyand,y=πxasodx=(aπ)dythe limits are as follows,

,x=a,y=π

x=ay=π

Substitute the above values.

V=mω22a(aπ)3ππy2sin2ydy=mω2a22(π)3ππy2(1cos2y2)dy=mω2a22π3[ππy2ππy2cos2ydy]=mω2a22π3[y33]ππy2sin2y2|π*ππ(2y)(sin2y2)dy

Evaluate the above expression further.

V=mω2a22π3[y36(y2418)sin2yycos2y4]ππ=mω2a24π2[2π23[16(2π3)14(πcos2π+πcos2π)]=mω2a22π3[π33π2]

Consequently, the minimum Hamiltonian is as follows,

Hmin=π222m((2π3/3)12)1/2mωπ2+mω24π2(2π231)π2(mω)(2(2π23)1)1/2=((2π3/3)12)1/2(ω2)+(2π231)ω4(2(2π2/3)1)1/2=((2π2/3)12)1/2(ω2)[1+(2π231)122(2π231)]=ω2[(2π2/3)12]1/2(2)=32ω[((2π2/3)12)1/2(23)]=(32)ω(1.857)=(32)ω

Thus, the first actual excited state energy is 32ωHmin>32ω.

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Most popular questions from this chapter

Evaluate Dand X(Equations and ). Check your answers against Equations 7.47and 7.48.

Suppose you’re given a two-level quantum system whose (time-independent) Hamiltonian H0admits just two Eigen states, Ψa (with energy Ea ), and Ψb(with energy Eb ). They are orthogonal, normalized, and non-degenerate (assume Ea is the smaller of the two energies). Now we turn on a perturbation H′, with the following matrix elements:

Ψa|H'|Ψa=Ψb|H'|Ψb=0;Ψa|H'|Ψb=Ψb|H'|Ψa (7.74).

where h is some specified constant.

(a) Find the exact Eigen values of the perturbed Hamiltonian.

(b) Estimate the energies of the perturbed system using second-order perturbation theory.

(c) Estimate the ground state energy of the perturbed system using the variation principle, with a trial function of the form

Ψ=(cosϕ)Ψa+(sinϕ)ψb (7.75).

where ϕ is an adjustable parameter. Note: Writing the linear combination in this way is just a neat way to guarantee that ψ is normalized.

(d) Compare your answers to (a), (b), and (c). Why is the variational principle so accurate, in this case?

Use a gaussian trial function (Equation 7.2) to obtain the lowest upper bound you can on the ground state energy of (a) the linear potential V(x)=α|x| (b) the quartic potential:V(x)=αx4

a) Use the variational principle to prove that first-order non-degenerate perturbation theory always overestimates (or at any rate never underestimates) the ground state energy.

(b) In view of (a), you would expect that the second-order correction to the ground state is always negative. Confirm that this is indeed the case, by examining Equation 6.15.

Suppose we used a minus sign in our trial wave function (Equation 7.37):ψ=A[ψ0(r1)-ψ0(r2)]): Without doing any new integrals, find F(x) (the analog to Equation ) for this case, and construct the graph. Show that there is no evidence of bonding. (Since the variational principle only gives an upper bound, this doesn't prove that bonding cannot occur for such a state, but it certainly doesn't look promising). Comment: Actually, any function of the form ψ=A[ψ0(r1)+eiϕψ0(r2)]has the desired property that the electron is equally likely to be associated with either proton. However, since the Hamiltonian (Equation 7.35 ) is invariant under the interchange P:r1r2 , its eigen functions can be chosen to be simultaneously eigen functions of P . The plus sign (Equation 7.37) goes with the eigenvalue +1 , and the minus sign (Equation 7.52 ) with the eigenvalue -1 ; nothing is to be gained by considering the ostensibly more general case (Equation 7.53), though you're welcome to try it, if you're interested.

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