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35. The Photoelectric Effect

Introduction

In these notes we consider the ejection of an atomic electron by an incident photon, which is an example of the photoelectric effect. The photon should have an energy in the ultraviolet to x-ray range, for reasons to be explained below; thus, our results will provide a semi-quantitative model for the absorption of x-rays by matter. In these notes, we use a version of the semiclassical theory of radiation, in which the radiation field is treated classically, but the atomic system quantum mechanically. Certain quantum mechanical concepts, notably photons, are used in the description of the classical radiation field. The photoelectric effect is not only interesting and important physically, but the following calculation also provides excellent exercise in time-dependent perturbation theory, the treatment of cross s, and assorted physical facts.

The Incident Photon

We suppose the incident photon has energy E0=ℏω0E_0=\hbar\omega_0 and momentum p0=ℏk0\pvec_0=\hbar\kvec_0. (We use the 0 subscript to refer to the incident photon; quantities without this subscript, such as EE or k\kvec, will refer to the ejected electron.) For simplicity, we assume the atom has a single electron (or a single electron of interest), and that it is initially in its ground state. We let EgE_g be the energy of this ground state; naturally, Eg<0E_g<0. Then by conservation of energy, we must have

ℏω0>∣Eg∣,\hbar\omega_0 > |E_g|,

so that the photon will have enough energy to eject the electron.

Actually, we will make a stronger assumption, namely,

ℏω0≫∣Eg∣,\hbar\omega_0 \gg |E_g|,

for the following reason. Assuming the atom is initially neutral, the ejected electron leaves a positive ion behind and travels out in the long-range Coulomb field of the ion. Therefore the final electron state is not that of a free particle, but rather one of the unbound or positive energy solutions of the Coulomb potential. The unbound Coulomb wave functions are important in many applications, and they can be determined by the usual methods for solving differential equations (power series, etc). These wave functions turn out to be hypergeometric functions, and for serious work involving Coulomb scattering and other applications one must know about them. Nevertheless, it would be simpler if we could deal with free particle wave functions for the final electron states. We can do this in a certain approximation if we assume that the energy of the ejected electron is much greater than the binding energy ∣Eg∣|E_g|, so that the ejected electron does not feel the Coulomb field very much. This is why we make the assumption (2), so that we can approximate the final electron wave functions by free particle solutions.

By energy conservation we have

ℏω0+Eg=E,\hbar\omega_0 + E_g = E,

where EE is the final electron energy. Under the condition (2), both ℏω0\hbar\omega_0 and EE will be large compared to ∣Eg∣|E_g|, and nearly equal to one another. Therefore we can rewrite the condition (2) in another form, and combine it with the condition that our electron be nonrelativistic, by writing

∣Eg∣≪E≪mc2.|E_g| \ll E \ll mc^2.

This can be put into dimensionless form by dividing by mc2mc^2,

(Zα)2≪Emc2≪1,(Z\alpha)^2 \ll {E\over mc^2} \ll 1,

where we use the estimate ∣Eg∣∼(Zα)2mc2|E_g| \sim (Z\alpha)^2 mc^2, valid for hydrogen-like atoms. For example, in the case of hydrogen, we might restrict the energy of the incident photon to lie in the range,

100 ev<≈ℏω0<≈100 Kev.100~ev <\approx \hbar\omega_0 <\approx 100~Kev.

Such photons lie in the far ultraviolet to x-ray region. If we were willing to deal with hypergeometric functions we could extend the lower limit downward; if we were willing to use relativistic quantum mechanics, we could extend the upper limit upwards. But we will live with the stated limits.

We will describe the incident photon by means of a classical light wave, with vector potential

A(x,t)=A0ϵei(k0⋅x−ω0t)+textc.c.,\Avec(\xvec,t) = A_0 \epsilonvec e^{i(\kvec_0\cdot\xvec-\omega_0t)} + \\textc.c.,

where A0A_0 is the amplitude (assumed to be real), and where ϵ\epsilonvec is the polarization unit vector (also assumed to be real, indicating linear polarization). This vector potential is in the Coulomb gauge (the scalar potential is taken to be zero), so that

∇⋅A=0,\del\cdot\Avec=0,

as follows by taking the divergence of (7) and using the transversality condition,

ϵ⋅k0=0.\epsilonvec\cdot\kvec_0=0.

The Atomic System

The atomic system for the one-electron atom described by the unperturbed Hamiltonian,

H0=p22m+V(x).H_0={p^2\over 2m} + V(\xvec).

For part of the following calculation we can leave V(x)V(\xvec) unspecified, but at a certain point we will specialize to a hydrogen-like atom with

V(x)=−Ze2r.V(\xvec) = -{Ze^2\over r}.

As mentioned, we assume that the atom is initially in its ground state ∣g⟩\ket{g} with energy EgE_g, so that

H0∣g⟩=Eg∣g⟩.H_0\ket{g} = E_g \ket{g}.

We will assume that the unbound electron in the final state is described by a plane wave with wave vector k\kvec,

ψk(x)=⟨x∣k⟩=eik⋅xV,\psi_\kvec(\xvec) = \braket{\xvec}{\kvec} = {e^{i\kvec\cdot\xvec} \over \sqrt{V}},

where we adopt box normalization as in (68)--(70). The final energy is denoted EE.

The perturbing Hamiltonian is

H1=emcp⋅A,H_1 = {e\over mc}\pvec\cdot\Avec,

which comes from expanding (1/2m)(p+eA/c)2(1/2m)(\pvec+e\Avec/c)^2 and dropping the term in A2\Avec^2. We note that p⋅A=A⋅p\pvec\cdot\Avec=\Avec\cdot\pvec because of the Coulomb gauge condition (8). We will also write the perturbing Hamiltonian in the form,

H1(t)=Ke−iω0t+K†e+iω0tH_1(t) = K e^{-i\omega_0t} + K^\hc e^{+i\omega_0t}

[see (43)], so that

K=eA0mc(ϵ⋅p)eik0⋅x.K = {eA_0\over mc} (\epsilonvec\cdot\pvec) e^{i\kvec_0\cdot\xvec}.

We drop the term in A2\Avec^2 because we will be working only to first order in perturbation theory; if we were to go to second order, this term would have to be included.

The Transition Rate

We can now proceed to the transition rate, which follows from (47) and which we write in the form,

w=2πℏ2∑k∣⟨k∣K∣g⟩∣2Δt(ω),w = {2\pi\over \hbar^2} \sum_\kvec |\matrixelement{\kvec}{K}{g}|^2 \Delta_t(\omega),

where

ω=E−ℏω0−Egℏ=1ℏ(ℏ2k22m−ℏω0−Eg).\omega={E-\hbar\omega_0-E_g \over \hbar} = {1\over\hbar} \Bigl( {\hbar^2 k^2 \over 2m} - \hbar\omega_0 - E_g \Bigr).

The sum in (17) is to be taken over final states which lie in a small cone of solid angle ΔΩ\Delta\Omega about some final wave vector kf\kvec_f, as in Fig.~\figr\tdpt.5. We choose the direction of kf\kvec_f to be some direction of interest, and we choose the magnitude of kf\kvec_f by conservation of energy, so that

ℏ2kf22m=ℏω0+Eg.{\hbar^2 k_f^2 \over 2m} = \hbar\omega_0 + E_g.

The notational difference between k\kvec and kf\kvec_f is that k\kvec is a variable final electron state over which we are summing, which does not necessarily conserve energy, while kf\kvec_f does conserve energy and is in some fixed direction of interest.

Next we make the replacement

w→dwdΩΔΩw \to \dod{w}{\Omega} \Delta\Omega

and the replacement (81) in (17), in order to go over to the transition rate per unit solid angle. This gives

dwdΩ=2πℏ2V(2π)3∫0∞k2 dk ∣⟨k∣K∣g⟩∣2Δt(ω),\dod{w}{\Omega} = {2\pi\over\hbar^2} {V\over(2\pi)^3} \int_0^\infty k^2 \, dk\, |\matrixelement{\kvec}{K}{g}|^2 \Delta_t(\omega),

which we will transform in various ways. First we must relate dw/dΩdw/d\Omega to the differential cross ,

dwdΩ=nividσdΩ,\dod{w}{\Omega} = n_i v_i \dod{\sigma}{\Omega},

where nin_i is the number density of the incident particles and viv_i is their velocity. But since the incident particles are photons, their velocity is vi=cv_i=c.

To compute nin_i we must mix classical and quantum concepts. An incident beam consisting of nin_i photons per unit volume has an energy density u=niℏω0u=n_i\hbar\omega_0; on the other hand, by classical electromagnetic theory we have u=(E2+B2)/8πu=(E^2+B^2)/8\pi. In the light wave (7) the electric and magnetic contributions to the energy density are equal, and cross terms vanish when we average over the volume of the box. Thus we find,

u=E2+B28π=ω02A022πc2=niℏω0,u={E^2+B^2\over 8\pi} = {\omega_0^2 A_0^2 \over 2\pi c^2} = n_i\hbar\omega_0,

or

ni=ω0A022πℏc2=k0A022πℏc,n_i = {\omega_0 A_0^2 \over 2\pi\hbar c^2} = {k_0 A_0^2 \over 2\pi\hbar c},

where we have used ω0=ck0\omega_0=ck_0. We now solve (22) for the cross , finding,

dσdΩ=2πℏk0A02dwdΩ.\dod{\sigma}{\Omega} = {2\pi\hbar \over k_0 A_0^2} \dod{w}{\Omega}.

The Matrix Element and Cross Section

Next we work on the right hand side of (21). First, we write out the matrix element, using (16),

⟨k∣K∣g⟩=eA0mc⟨k∣(ϵ⋅p)eik0⋅x∣g⟩=eA0ℏmc(ϵ⋅k)⟨k∣eik0⋅x∣g⟩,\matrixelement{\kvec}{K}{g} = {eA_0\over mc} \matrixelement{\kvec} {(\epsilonvec\cdot\pvec) e^{i\kvec_0\cdot\xvec}}{g} = {eA_0\hbar\over mc} (\epsilonvec\cdot\kvec) \matrixelement{\kvec}{e^{i\kvec_0\cdot\xvec}}{g},

where in the final step we have allowed the momentum operator p\pvec to act to the left on the plane wave state ⟨k∣\bra{\kvec}, bringing out a factor of ℏk\hbar\kvec. The remaining matrix element can be expressed in terms of the Fourier transform of the ground state wave function ψg(x)=⟨x∣g⟩\psi_g(\xvec)=\braket{\xvec}{g},

⟨k∣eik0⋅x∣g⟩=1V∫d3x e−i(k−k0)⋅x ψg(x)=(2π)3/2Vψ~g(q),\matrixelement{\kvec}{e^{i\kvec_0\cdot\xvec}}{g} = {1\over\sqrt{V}} \int d^3\xvec \, e^{-i(\kvec-\kvec_0)\cdot\xvec} \, \psi_g(\xvec) = {(2\pi)^{3/2}\over \sqrt{V}} \tilde \psi_g(\qvec),

where

q=k−k0\qvec=\kvec-\kvec_0

and where

ψ~g(q)=∫d3x(2π)3/2 e−iq⋅x ψg(x).\tilde \psi_g(\qvec) = \int {d^3\xvec \over (2\pi)^{3/2}} \, e^{-i\qvec\cdot\xvec} \, \psi_g(\xvec).

Finally, we transform the function Δt(ω)\Delta_t(\omega) in (21), using (18) and (19):

Δt(ω)→δ(ω)=mℏkδ(k−kf).\Delta_t(\omega) \to \delta(\omega) = {m\over \hbar k} \delta(k-k_f).

At this point we remark that had we been doing a problem in the emission or absorption of optical radiation from an atom, we would have been able to expand the exponential eik0⋅xe^{i\kvec_0\cdot\xvec} in (26), since radiation in this frequency range satisfies k0r≪1k_0r \ll 1 (the wavelength is much larger than the atomic size). This would lead to the multipole expansion (the dipole approximation at lowest order). We cannot make this expansion in the present calculation, however, because we are dealing with radiation of short wavelength, such as x-rays.

We now gather all the pieces together [(25), (21), (26), (27) and (30)] to obtain

dσdΩ=2πℏk0A022πℏ2V(2π)3∫0∞k2 dk e2A02ℏ2m2c2(ϵ⋅k)2(2π)3V∣ψ~g(q)∣2mℏkδ(k−kf),\dod{\sigma}{\Omega} = {2\pi\hbar\over k_0 A_0^2} {2\pi\over\hbar^2} {V\over (2\pi)^3} \int_0^\infty k^2 \, dk \, {e^2 A_0^2 \hbar^2 \over m^2 c^2} (\epsilonvec\cdot\kvec)^2 {(2\pi)^3\over V} |\tilde\psi_g(\qvec)|^2 {m\over \hbar k} \delta(k-k_f),

or,

dσdΩ=(2π)2e2mc2kfk0(ϵ⋅kf)2∣ψ~g(q)∣2,\dod{\sigma}{\Omega} = (2\pi)^2 {e^2\over mc^2} {k_f\over k_0} (\epsilonvec\cdot\kvec_f)^2 |\tilde\psi_g(\qvec)|^2,

where now q=kf−k0\qvec=\kvec_f-\kvec_0. We see that all the volume factors cancel out of (31), as they should, as do the factors of A0A_0, which we expect because a cross by definition is independent of the incident flux. The vector q=kf−k0\qvec=\kvec_f-\kvec_0 reminds us of the momentum transfer vector kf−ki\kvec_f-\kvec_i which occurred in our analysis of elastic scattering in 34. Time-Dependent Perturbation Theory, but here the quantity ℏq\hbar\qvec is the momentum difference between the final electron and the initial photon. Unlike the case of elastic scattering, where we had kf=kik_f=k_i, here the vectors kf\kvec_f and k0\kvec_0 are of different magnitudes.

Momentum Transfer

The fact that the vector q\qvec is nonzero means that a proper understanding of momentum conservation must take into account the nucleus as well as the photon and the electron. The reason the nuclear momentum has not appeared explicitly in our calculations is that we implicitly assumed in writing down (10) that the nuclear mass was infinitely large in comparison to the electron mass. This of course is a good approximation, and it means that the nucleus can carry off a large amount of momentum without moving very fast. In the limit of infinite nuclear mass, the nucleus acts like a momentum source or sink which is able to provide whatever momentum is needed for the reaction at hand. This is important, because in the absence of such a momentum source, a reaction such as

γ+e→e,\gamma +e \to e,

that is, the absorption of a photon by a free electron, is impossible (one cannot satisfy both energy and momentum conservation in this reaction). Similarly, in the absence of a momentum source, the reaction

e→e+γe \to e +\gamma

is impossible. But if there is a nucleus nearby to take up some momentum, then the reaction (34) does occur; this is called Bremsstrahlung (German for “braking radiation”), and it is one of the principal mechanisms for the slowing down of fast charged particles in matter (especially important for light particles like electrons and muons). Our assumption of infinite nuclear mass in the present calculation has caused the conservation of momentum to appear only implicitly, in contrast to the conservation of energy, which is explicitly expressed by the δ\delta-function in (31).

We have written the cross (32) so that the classical radius of the electron rer_e makes its appearance,

re=e2mc2=α2a0=2.82×10−13cm.r_e = {e^2\over mc^2} = \alpha^2 a_0 =2.82 \times 10^{-13} cm.

This radius is called classical because there is no ℏ\hbar in it; its physical meaning is that it is the radius (to within an order of magnitude) outside of which the electrostatic energy of the nominal monopole field (divided by c2c^2) equals the mass of the electron. The total electrostatic energy in the field of a monopole is, of course, infinite.

To proceed with the analysis, we will now assume that V(r)=−Ze2/rV(r)=-Ze^2/r, for a hydrogen-like atom. Then the ground state wave function is

ψg(x)=1πa3 e−r/a,\psi_g(\xvec) = {1\over \sqrt{\pi a^3}} \, e^{-r/a},

where a=a0/Za=a_0/Z and a0a_0 is the usual Bohr radius. It is then straightforward to compute the Fourier transform, according to (29). We find

ψ~g(q)=1π(2a)3/2(1+a2q2)2.\tilde \psi_g(\qvec) = {1\over \pi} {(2a)^{3/2} \over (1+a^2q^2)^2}.

This is obviously proportional to the momentum-space wave function of the ground state of the hydrogen atom; notice that it is a rational function of the momentum. In any case, the cross now becomes

dσdΩ=32e2mc2kfk0∣ϵ⋅kf∣2a3(1+a2q2)4.\dod{\sigma}{\Omega} = 32 {e^2 \over mc^2} {k_f \over k_0} |\epsilonvec\cdot\kvec_f|^2 {a^3 \over (1+a^2q^2)^4}.

Approximating the Cross Section

This cross can be boiled down further by incorporating the approximation (4). This occurs in two steps. First, it turns out that the initial photon wave number k0k_0 is much smaller than the final electron wave number kfk_f. To show this, we write out the conservation of energy equation (3) in the form

ℏω0=ℏck0≈ℏ2kf22m,\hbar\omega_0 = \hbar ck_0 \approx {\hbar^2 k_f^2 \over 2m},

where we neglect EgE_g in comparison to ℏω0\hbar\omega_0. But this can be put in the form,

k0kf≈ℏkf2mc=pf2mc=vf2c≪1,{k_0\over k_f} \approx {\hbar k_f \over 2mc} = {p_f\over 2mc} = {v_f\over 2c} \ll 1,

where pfp_f and vfv_f are the final electron momentum and velocity, respectively, and where we make use of the nonrelativistic assumption E≪mc2E\ll mc^2. We see that k0/kfk_0/k_f is indeed small, of the order of vf/cv_f/c, and for consistency in a nonrelativistic treatment, we should neglect terms of relative order

(k0kf)2∼(vfc)2.\Bigl( {k_0\over k_f} \Bigr)^2 \sim \Bigl( {v_f \over c} \Bigr)^2.

For example, the quantity q2q^2, which occurs in the cross (38), can be approximated,

q2=(kf−k0)2≈kf2−2kf⋅k0=kf2−2kfk0cos⁡θ\begin{aligned} q^2 &= (\kvec_f - \kvec_0)^2 \approx k_f^2 -2\kvec_f\cdot\kvec_0 = k_f^2 - 2k_f k_0 \cos\theta \end{aligned}
=kf2(1−vfccos⁡θ),\begin{aligned} &= k_f^2 \Bigl( 1 - {v_f\over c} \cos\theta \Bigr), \end{aligned}

where we neglect terms of relative order (k0/kf)2(k_0/k_f)^2. This is the first approximation.

On the other hand, we also have

a2kf2=2ma2ℏ2ℏ2kf22m∼ℏ2Z2me4E∼E∣Eg∣≫1,a^2k_f^2 = {2ma^2\over \hbar^2} {\hbar^2 k_f^2 \over 2m} \sim {\hbar^2\over Z^2 m e^4} E \sim {E \over |E_g|} \gg 1,

so that

1+a2q2≈a2kf2(1−vfccos⁡θ).1+a^2q^2 \approx a^2 k_f^2 \Bigl( 1 - {v_f\over c}\cos\theta \Bigr).

This is the second approximation.

Coordinates for the photoelectric effect.

Figure 1:Coordinates for the photoelectric effect.

Angular Dependence and Total Cross Section

We now introduce coordinates, as illustrated in Figure 1. We assume the atom is at the origin, and that the photon comes in along the negative zz-axis, so that k0=k0z^\kvec_0 = k_0{\hat{\mathbf{z}}}. The photon is assumed to be linearly polarized in the xx-direction, so that ϵ=x^\epsilonvec={\hat{\mathbf{x}}}. The ejected electron goes out in the direction (θ,ϕ)(\theta,\phi).

With the geometry indicated in Figure 1 and the approximations (43) and (45), we can simplify the cross (38). We find

dσdΩ=32k0(e2mc2)1(kfa)5sin⁡2θcos⁡2ϕ[1−(vf/c)cos⁡θ]4.\dod{\sigma}{\Omega} = {32\over k_0} \Bigl( {e^2\over mc^2} \Bigr) {1 \over (k_fa)^5} {\sin^2\theta \cos^2\phi \over [1 - (v_f/c)\cos \theta]^4}.

This is the cross for linear polarization in the xx-direction. If we had had linear polarization in the yy-direction, we would have obtained sin⁡2ϕ\sin^2 \phi in (46) instead of cos⁡2ϕ\cos^2\phi. To deal with the case of unpolarized light, we must average over initial polarizations; this can be carried out formally by using a density matrix for the photons, but in the present case it amounts to adding sin⁡2ϕ\sin^2\phi and cos⁡2ϕ\cos^2\phi and dividing by 2. If we also expand the denominator to first order in vf/cv_f/c, we obtain

(dσdΩ)unpol=16k0(e2mc2)1(kfa)5sin⁡2θ(1+4vfccos⁡θ).\Bigl(\dod{\sigma}{\Omega}\Bigr)_unpol = {16\over k_0} \Bigl( {e^2\over mc^2} \Bigr) {1\over(k_fa)^5} \sin^2\theta \Bigl( 1 + 4{v_f\over c}\cos\theta \Bigr).

Finally, we can integrate this over all solid angles of the final ejected electron, whereupon the term in cos⁡θ\cos\theta disappears, to obtain the total cross for unpolarized radiation,

σtot=128π31k0(e2mc2)1(akf)5.\sigma_tot = {128 \pi \over 3} {1\over k_0} \Bigl( {e^2\over mc^2} \Bigr) {1\over (ak_f)^5}.

The total cross can be written in various ways; for example, we can express it in terms of the incident photon energy E0=ℏω0E_0 =\hbar\omega_0 and the Bohr radius a0a_0 of hydrogen:

σtot=16π23α8Z5a02(mc2E0)7/2,\sigma_tot = {16\pi\sqrt{2}\over 3} \alpha^8 Z^5 a_0^2 \Bigl( {mc^2 \over E_0} \Bigr)^{7/2},

where α\alpha is the fine structure constant. In this form the cross is manifestly an area, since a02a_0^2 is essentially the cross-al area of a hydrogen atom. This area is reduced by the very small factor α8\alpha^8, but magnified by the presumably large factor (mc2/E0)7/2(mc^2/E_0)^{7/2} (because of the nonrelativistic assumption E≪mc2E\ll mc^2), and by the possibly large factor Z5Z^5. Although this formula was derived only for a hydrogen-like atom, it is valid in a semiquantitative way for the ejection of KK-shell electrons by x-rays in any atom. The strong ZZ-dependence indicates that heavier atoms are more effective in stopping x-rays, and the strong inverse energy dependence indicates that hard x-rays are more penetrating than soft ones.

Problems

Problem 1.

X-rays of energy E0E_0 that are linearly polarized in the xx-direction are incident upon positronium in the ground state. The beam of x-rays is directed in the +z+z direction. The positronium atom'' is at rest. Find the differential cross section $d\sigma/d\Omega$ for the x-ray to break the atom’’ apart, where Ω\Omega refers to the direction of the ejected electron. Assume

e2a0≪E0≪mc2,{e^2\over a_0} \ll E_0 \ll mc^2,

where a0a_0 is the usual (hydrogen) Bohr radius, and make approximations this set of notes. In particular, expand your answer through first order in vf/cv_f/c. Find the total cross and express it as a function of E0E_0, and as a multiple of a02a_0^2.

Note that the light wave interacts with both the electron and the positron; therefore you must set up a two-particle Hamiltonian.