The Asymptotic normalization coefficient or the ANC is thought to be an alternative to the spectroscopic factor. As the name suggested, this is the coefficient for asymptote of the radial wave function.
For a single nucleon adding/removal reaction, the reaction probability is
Assume the interaction only acts on the nucleon that being add or remove, thus
which is the bound state wave function. Due to the nuclear interaction, the bound state wave function most probably not normalized. In other point of view, suppose the nucleus B = A + 1, the wave function of nucleus B could be
where is an orbital, is the -th excited state of nucleus A, and the square bracket is the angular coupling, antisymmetric, and normalization operator. As the wave function of nucleus B must be normalized, Thus,
.
And the bound state can be approximated
.
The spectroscopic factor of orbital in this A + 1 = B reaction is
At far away distance, the nucleus potential is very weak or effectively zero. The Schrodinger equation becomes
where . The Coulomb potential is still here because it is a long range force. Separate the radial and angular part,
This radial equation was solved before in this post. There are two solutions for , one is bound (in mathematics) and one is unbound. I state the mathematically-bounded solution in here
There is another Coulomb wave function , although there is no simple form of the function, the two Coulomb wave function, one behave like a sine wave ( ) another one behave like a cosine wave (), they can be combined into a complex function, the Coulomb Hankel function, (it is different from the Hankel function of the first and second kind )
where is the confluent hypergeometric function of the second kind. In Mathematica, the function is given is built-in
HypergeometrixU[l+1+i eta, 2l+2, -2 i r]
And
We can see, the analogy
The long range (unbound, scattering) behaviour of the Coulomb wave function is
where is the Coulomb phase shift.
The ANC is the coefficient between the bound state wave function and the Coulomb wave function at . Since it is the bound state long range behaviour, , we have to use the Coulomb Hankel function.
For neutron,
We can see that, when , the $latex H_0^\pm (i \kappa r, 0 ) = e^{-\kappa r} is a bounded and real solution.
This is the same for higher that the decay factor appeared in the Hankel function.
In the following, we use the neutron and simplify the Coulomb wave function for few . When no charge, . And since it is a bound state,
In fact, the solution for is the Spherical Bessel function J. As the is pure imaginary, and we know that the Spherical Bessel function J and Y are unbound for pure imaginary position.
The solution is the Spherical Hankel function . This is the Coulomb Hankel function divided by the radius. In Mathematica, the built-in function is
SphericalHankelH1[l, i kappa r]
In fact,
In this paper N.K. Timofeyuk, PRC 88, 044315 (2013), in equation 3, the Whittaker function should be the Whittaker W-function. In Mathematica
WhittakerW[ - i eta, l + 1/2, 2 kappa r ]
The difference between the Whittaker W-function and the Hankel function with complex argument is the normalization factor
Since the ANC is the proportional factor between the bound state wave function and the Whittaker W-function (or the Coulomb wave function, or the spherical Hankel function ), so the normalization factor is important.
As we know that the neutron should behave as Spherical Hankel function, thus, we checked that
where is the modified Bessel function of the 2nd kind. Here are a list of the Whittaker W-function for
For me, the problem of the ANC is that, the Coulomb Hankel function or the Whittaker W-function cannot be normalized. And without a proper normalization, how can we compare the magnitude of two wave functions??
For example, I calculated the 1s1/2 bound state wave function from a Woods-Saxon potential for neutron. The parameters are , the energy is -2.227 MeV and . And here is the comparison
The Woods-Saxon bound state is supposed to be a pure wave function that has SF = 1 or ANC = 1. But since the Whittaker cannot be normalized, and depends on the “definition”, where the appears in the denominator or not, the ANC can be different. And for this example the ANC = 0.7, for a pure state.