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Question: In the text I asserted that the first-order corrections to an n-fold degenerate energy are the eigen values of the Wmatrix, and I justified this claim as the "natural" generalization of the case n = 2.

Prove it, by reproducing the steps in Section 6.2.1, starting with

ψ0=j=1nαjψj0

(generalizing Equation 6.17), and ending by showing that the analog to Equation6.22 can be interpreted as the eigen value equation for the matrix W.

Short Answer

Expert verified

The analog function can be interpreted as the eigenvalue equation for the matrix W.

Step by step solution

01

Significance of Schrodinger’s equation

The Schrodinger wave equation is a linear partial differential equation that governs the wave function of the Quantum Mechanical System.

The following can be interpreted from the equation.

H^ψ=Eψand H^0ψ0=E0ψ0andH^=H^0+λH^

02

Determination of the eigenvalues

Write equation 6.17.

ψ0=αψa0+βψb0

Write equation 6.22.

αWaa+βWab=αE1

It is known that En=En6+λEn1+λ2En2+...and ψ=ψ0+λψ1+λ2ψ2+...and ψ0=j=1nαfψj0

Apply Schrodinger's equation.

H^0+λH^=ψ0+λψ1+λ2ψ2+...=(En0+λEn1+λ2En2+...)ψ0+λψ1+λ2ψ2+...=H^0ψ0+λH^0ψ1+H^'ψ0+λ2H^0ψ2+H^'ψ1+...=En0ψ0+λEn0ψ0+En1ψ0+λ2En0ψ2+En1ψ1+En2ψ0+...

Obtain the first-order correction for the energy eigen values by equating the coefficients of the same order.

=H0ψ1+H^'ψ0=En0ψ1+E1ψ0

Multiply both sides by ψ_j0*.

ψj0H^0ψ1+ψj0H^'ψ0=En0ψj0ψ1+En1ψj0ψ0

It is known thatψ0=j=1nαfψj0 and(ψ0H^0=En0*(ψ0,H^'=H^0* , . Then the

role="math" localid="1658211098621" En0=En0(ψ0H^0=En0*(ψ0

Write the generalized form of the equation.

En0ψj0ψ1+ψj0H^'ψ0=En0ψj0ψ1+En1ψj0ψ0j=1nαjψj0H^'ψ0=En1j=1nαjψj0ψj0j=1nαjWij=En1j=1nαjWij

Thus, the analog function can be interpreted as the eigenvalue equation for the matrix W.

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Most popular questions from this chapter

Sometimes it is possible to solve Equation 6.10 directly, without having to expand ψ1nin terms of the unperturbed wave functions (Equation 6.11). Here are two particularly nice examples.

(a) Stark effect in the ground state of hydrogen.

(i) Find the first-order correction to the ground state of hydrogen in the presence of a uniform external electric field (the Stark effect-see Problem 6.36). Hint: Try a solution of the form

(A+Br+Cr2)e-r/acosθ

your problem is to find the constants , and C that solve Equation 6.10.

(ii) Use Equation to determine the second-order correction to the ground state energy (the first-order correction is zero, as you found in Problem 6.36(a)).

Answer:-m(3a2eEext/2h)2

(b) If the proton had an electric dipole moment p the potential energy of the electron in hydrogen would be perturbed in the amount

H'=-epcosθ4π00r2~

(i) Solve Equation 6.10 for the first-order correction to the ground state wave function.

(ii) Show that the total electric dipole moment of the atom is (surprisingly) zero, to this order.

(iii) Use Equation 6.14 to determine the second-order correction to the ground state energy. What is the first-order correction?

Calculate the wavelength, in centimeters, of the photon emitted under a hyperfine transition in the ground state (n=1) of deuterium. Deuterium is "heavy" hydrogen, with an extra neutron in the nucleus; the proton and neutron bind together to form a deuteron, with spin 1 and magnetic moment

μdl=gde2mdSd

he deuteron g-factor is 1.71.

Suppose we perturb the infinite cubical well (Equation 6.30) by putting a delta function “bump” at the point(a/4,a/2,3a/4):H'=a3V0δ(x-a/4)δ(y-a/2)δ(z-3a/4).

Find the first-order corrections to the energy of the ground state and the (triply degenerate) first excited states.

Question: Sometimes it is possible to solve Equation 6.10 directly, without having to expand in terms of the unperturbed wave functions (Equation 6.11). Here are two particularly nice examples.

(a) Stark effect in the ground state of hydrogen.

(i) Find the first-order correction to the ground state of hydrogen in the presence of a uniform external electric fieldEext (the Stark effect-see Problem 6.36). Hint: Try a solution of the form

(A+Br+Cr2)e-r/acosθ

your problem is to find the constants , and C that solve Equation 6.10.

(ii) Use Equation to determine the second-order correction to the ground state energy (the first-order correction is zero, as you found in Problem 6.36(a)). Answer:-m(3a2eEext/2)2 .

(b) If the proton had an electric dipole moment p the potential energy of the electron in hydrogen would be perturbed in the amount

H'=-epcosθ4π̀o0r2

(i) Solve Equation 6.10 for the first-order correction to the ground state wave function.

(ii) Show that the total electric dipole moment of the atom is (surprisingly) zero, to this order.

(iii) Use Equation 6.14 to determine the second-order correction to the ground state energy. What is the first-order correction?

Estimate the correction to the ground state energy of hydrogen due to the finite size of the nucleus. Treat the proton as a uniformly charged spherical shell of radius b, so the potential energy of an electron inside the shell is constant:-e2/(4πϵ0b);this isn't very realistic, but it is the simplest model, and it will give us the right order of magnitude. Expand your result in powers of the small parameter, (b / a) whereis the Bohr radius, and keep only the leading term, so your final answer takes the form ΔEE=A(b/a)n. Your business is to determine the constant Aand the power n. Finally, put in b10-15m(roughly the radius of the proton) and work out the actual number. How does it compare with fine structure and hyperfine structure?

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