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Although the Schrödinger equation for helium itself cannot be solved exactly, there exist “helium-like” systems that do admit exact solutions. A simple example is “rubber-band helium,” in which the Coulomb forces are replaced by Hooke’s law forces:

H=-ħ22m(12+22)+12mω2|r1-r1|2(8.78).

(a) Show that the change of variables from

r1,r2,tor1,r2,tou12(r1+r2),v12(r1+r2) (8.79).

turns the Hamiltonian into two independent three-dimensional harmonic oscillators:

H=[-ħ2mu2+12mω2u2]+[-ħ2mu2+121-λmω2u2](8.80)

(b) What is the exact ground state energy for this system?

(c) If we didn’t know the exact solution, we might be inclined to apply the method of Section 7.2 to the Hamiltonian in its original form (Equation 7.78). Do so (but don’t bother with shielding). How does your result compare with the exact answer? Answer:(H)=3ħω(1-λ/4)a.

Short Answer

Expert verified

(a) Required equation is proved.

(b)Egs=32ħω(1+1-λ)

(c)Egs32ħω(1+1-12ħ)=3ħω(1-λ4)

Step by step solution

01

(a)Showing the changes of variables

r1=12(u+v);r2=12(u-v);r12+r22=12(u2+2uv+v2+u2-2uv+v2)=u2+v2(12+22)f(r1,r2)=2fx12+2fy12+2fz122fx22+2fy22+2fz22fx1=fuxuxx1+fvxvxx1=12fux+fvx;fx2=fuxuxx2+fvxfx1=12x1fu1+fvx=122fux2uxx1+2fuxvxvxx1+2fuxux

=122fux2+22fuxvx+2fvx2.2x22=12x2fux-fvx=122fux2uxx2+2fuxvxvxx2-2fv2uxuxx2-2fv2xvxx2.=122fux2-22fuxvx+2fvx2.So2fx12+2fx22=2fux2+2fvx2,andlikewiseforyandz:12+22=u2+v2.H=ħ22mu2+v2+122u2+v2-λ422v2H=-ħ22mu2+122u2+ħ22mv2+122u2-12λmω2v2

02

(b) The exact ground state energy 

The energy is

32ħωfortheupartand32ħω1-λforthevpart:Egs=32ħω1+1-λ.

03

(c) The ground state for one dimension oscillator 

The ground state for a one-dimensional oscillator is

ψ0(x)=mω1/4πe-max2/2(Eq.2.60)So,fora3-Doscillator,thegroundstateisisψ0(r)=π3/4e-mωr2/2andfortwoparticlesΨr1,r2=π3/4e-2r21,r22(ThisistheanalogtoEq.7.18.)Ψr1,r2Ψ100r1Ψ100r2=8πa3e-2r1,r2/aH=32ω+32ω+Vee=3ω+Vee(TheanalogtoEq.7.20).H=8E1+Vee(8.20).

localid="1655995511764" Vee=-λ4mω2mωπħ3e-mωħr12+r22r1-r22r12-2r1-r2+r22d3r1d3r2Vee=e24π00,8πa32e-4r1+r2/ar1-r2d3r1d3r2Ther1,r2termintegratestozero,bysymmetry,andther22termisthesameasther12term,soVee=-λ4mω2mωπħ3e-mωħr12+r22r12d3r1d3r2.=-λ4mω2mωπħ34π2000e-mωr22/ħr22dr2000e-mωr12/ħr14dr1.=-λ8m4ω5πħ314ħmωπħmω38ħmω2πħmω=-34λħω.H=3ħω-34λħω=3ħω1-λ4.Thevariationprinciplesaysthismustexceedtheexactground-stateenergy(b);letscheckit:

3ħω1-λ4>32ħω1+1-λ2-λ2>1+1-λ1-λ2>1-λ1-λ-λ24>1-λ.Itchecks.Infact,expandingtheexactanswerinpowersofλ,Egs32ħω1+1-12λ=3ħω1-λ4,werecoverthevariationresult.

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Most popular questions from this chapter

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

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.

Find the lowest bound on the ground state of hydrogen you can get using a Gaussian trial wave function

ψ(r)=Ae-br2,

where A is determined by normalization and b is an adjustable parameter. Answer-11.5eV

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

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.

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