This derives the multipole matrix elements corresponding to a single particle in an atom or nucleus. These will normally still need to be summed over all particles.
Both a basis of linear momentum photon wave functions and of angular
momentum ones are covered. For the angular momentum wave functions,
the long wave length approximation will be made that
is small.
Here
is the photon wave number and
the typical size of atom or
nucleus.
The derivations include a term due to an effect that was mentioned in the initial 1952 derivation by B. Stech, [42]. This effect is not mentioned in any textbook that the author is aware off. That seems to be unjustified. The term does not appear to be small for nuclei, but at the very least comparable to the usual electric multipole element given.
The rules of engagement are as follows:
The convoluted derivations in this note make use of a trick. Since “trick” sounds too tricky, it will be referred to as:
Lemma 1: This lemma allows you to get rid of derivatives on the wave function. The lemma assumes nonrelativistic particles. It is a generalization of a derivation of [15].
The lemma says that if
is the number of a particle in the atom or
nucleus, and if
is any function of the position of that particle
,
| (D.26) |
The energy difference can be expressed in terms of the energy
of the nominal photon emitted in the transition,
Note that none of my sources includes the commutator in the first
term, not even [15]. (The original 1952 derivation by
[42] used a relativistic Dirac formulation, in which the
term appears in a different place than here. The part in which it
appears there is small without the term and is not worked out with it
included.) The commutator is zero if the potential
only depends
on the position coordinates of the particles. However, nuclear
potentials include substantial momentum terms.
To prove the lemma, start with the left hand side
Now note the nonrelativistic eigenvalue problems for the two states

This requires in addition:
Lemma 2: This lemma allows you to express a certain
combination of derivatives in terms of the angular momentum operator.
It will be assumed that vector
is normal to vector
.
In that case:
The objective is now to use these lemmas to work out the matrix element
To reduce this, take the factor ![]()
![]()
out of
and write the
exponential in a Taylor series:
Plugging these results back into the expression for the matrix
element, renotating
into
for the first part of (1), into
for the second part, which can then be combined with the
first part, and into
for (2), and cleaning up gives the final
result:
The commutator is zero if the potential depends only on position. That is a valid approximation for electrons in atoms, but surely not for nuclei. For these it is a real problem, {N.14}.
For addendum {A.25}, the constant
should be taken
equal to ![]()
![]()
.
.
This subsection works out the details of the matrix element when angular momentum modes are used for the photon wave function.
The first matrix element to find is
Note that the electric multipole vector potential is closely related
to the magnetic one:
The expression for the electric potential can be simplified for
long photon wave lengths. Note first that
Long photon wave length corresponds to small photon wave number
.
terms above can then be ignored and in addition
the following approximation for the Bessel function applies,
{A.6},
That allows lemma 1 to be used to find the electric matrix element.
![\begin{eqnarray*}
H_{21,i}^{\rm E\ell 1} & = & - \frac{q_i}{m_i}
\langle\psi...
...ar\omega,r_i^\ell Y_{\ell i}^{m*}]
\vert\psi_{\rm {H}}\rangle
\end{eqnarray*}](img6688.gif)
The commutator is again negligible for atoms, but a big problem for nuclei, {N.14}.
There is also a term due to the interaction of the spin with the
magnetic field, given by the curl of
as already found above,
The third matrix element to find is the magnetic multipole one
It follows that
There is also a term due to the interaction of the spin with the
magnetic field, given by the curl of
,
,
The orbital and spin matrix elements may be combined into one as
This subsection explains where the radial, angular, and momentum factors in the Weisskopf and Moszkowski estimates come from. These factors represent the nondimensionalized matrix elements.
The electric matrix element is simplest. It is, written out in
spherical coordinates using the assumed wave functions,
The Weisskopf and Moszkowski estimates assume that the radial parts of
wave functions equal a constant
until the nuclear edge
and are
zero outside the nucleus. To perform the radial integral is then
straightforward:
The angular integral above is more tricky to ballpark. First of all,
it will be assumed that the matrix element of interest is the lowest
multipole order allowed by angular momentum conservation. That seems
reasonable, given that normally higher multipole transitions will be
very much slower. It follows that
.
The change in orbital angular momenta could in principle be up to one
unit different from the change in net angular momenta because of the
spins. But parity conservation allows only
.
To simplify even further, assume the following specific angular
states:
One glaring deficiency in the above analysis was the assumption that
the initial proton state was a
one. It would
certainly be reasonable to have an initial nuclear state that has
orbital angular momentum
and total angular
momentum
.
.
.
Fortunately, it turns out that this makes no difference. For example,
by symmetry the state
decays just as happily to
as
does to
.
it is a bit more nuanced. They produce an
initial state of the form:
So as long as the final state
has zero orbital angular
momentum, the decay is at 1 Weisskopf unit. The orientation of the
initial state makes no difference. That is reflected in table
A.3. This table lists the angular factors to be applied
to the Weisskopf unit to get the actual decay rate. The first row
shows that, indeed, when the final angular momentum is
,
,
More interesting is the possibility that the two states are swapped. Then the initial state is the one with zero orbital angular momentum. It might at first seem that that will not make a difference either. After all, decay rates between specific states are exactly the same.
But there is in fact a difference. Previously, each initial nucleus
had only two states to decay to: the spin-up and the spin-down version
of the final state. Now however, each initial nucleus has
,
final states it can decay to,
corresponding to the possible values of the final magnetic quantum
number
.
faster than the Weisskopf unit.
So by symmetry each nucleus of the pair decays
times faster
than the Weisskopf unit. That is reflected in the first column of
table A.3. (Recall that
is the difference in the
values.)
If neither the initial nor final state has zero orbital angular momentum, it gets more messy. Figuring out the correction factor in that case is something for those who love abstract mathematics.
Next consider magnetic multipole transitions. They are much messier
to ballpark. It will again be assumed that the multipole order is the
smallest possible. Unfortunately, now the final orbital angular
momentum cannot be zero. Because of parity, that would require that
the initial orbital angular momentum would be
.
Now consider the form of the magnetic matrix element
(A.181). First note, {D.43.2}, that the
angular momentum and gradient factors commute. That helps because
then the angular momentum operators, being Hermitian, can be applied
on the easier state
.
The
-
components of the angular momentum
operators leave the state
essentially unchanged. They
merely multiply the two terms by the eigenvalue
respectively
.
Next, this gets multiplied by the
-
stays spin-down. That cannot match the
spin-up of
.
The second term in
has the right spin. Since spin
states are orthonormal, their inner product produces 1. But now there
is a problem of matching the magnetic quantum number of
.
in the gradient. The gradient
reduces it to a combination of harmonic polynomials of one degree
less, in other words, to
polynomials.
That limits
to a value no larger than
,
has magnetic quantum number 0, the
value
in
cannot be matched. The bottom line is
that the
-
However, the
-
-
and
states. In particular, the
and
components of spin will
produce a spin-up version of the first term in
.
and a nonzero
contribution results. Similarly, the orbital angular momentum
operators will produce an
1 version of the second
term in
.
units from
the gradient, that is enough to match the magnetic quantum number of
.
Now it is just a matter of working out the details to get the complete
matrix element. The information in chapter 12.11 can be used
to find the exact states produced from
by the
and
angular momentum operators. Each state is a multiple of the
state. As far as the gradient term is concerned, the
harmonic polynomials are of the general form
A similar analysis shows that the given initial state cannot decay to
the version of the final state with negative magnetic quantum number
.
And of course, if the initial and final states are swapped, there is
again a factor
increase in decay rate.
More interestingly, the same expression turns out to hold if neither
the initial nor the final angular momentum equals
,
and that
The momentum factors (A.189) were identified using a computer program. This program crunched out the complete matrix elements using procedures exactly like the ones above. This program was also used to create table A.3 of angular factors. This guards against typos and provides an independent check on the Clebsch-Gordan values.