1. Introduction
In the first experiments, the purpose of which was to study the time delays of electrons in atomic photoeffect, electrons with the wave vector 
k emitted along the polarization vector 
e of the absorbed photon were recorded [
1,
2,
3]. With this experimental technique, the delay times of the electrons escaping at an arbitrary angle to the vector 
e were unknown. Now, investigations of time delays as a function of the emission angle 
 have become available [
4,
5,
6,
7], and the corresponding calculations have been able to reproduce this dependence for different atoms [
8,
9,
10,
11,
12,
13]. The electron delay time is a function depending on both the photoelectron emission angle 
 with respect to the radiation polarization vector 
e and the photoelectron energy 
E. In most calculations of the time delay, its dependence on the energy 
E is analyzed at fixed values of the angle 
, revealing the pronounced angle dependence for large emission angles.
The angular dependence of the time delay of the wave packet scattered (or emitted) by a spherical target was obtained by Froissard, Goldberger, and Watson in [
14], where the following expression for the angular time delay of the packet scattered in the direction 
 was derived:
Here, 
 denotes the amplitude of electron elastic scattering by a target [
15]
      
      where 
 is the partial scattering phase shifts and 
 are the Legendre polynomials. According to (
1), the forward scattering 
 must be excluded due to the interference effects between the forward scattered wave and the incident wave that give rise to the optical theorem [
15].
The domain of applicability of the 
angular time delay  (
1) is considerably broader than that of the Eisenbud–Wigner–Smith (EWS) partial-wave time delay [
16,
17,
18]
      
In particular, Equation (
1) serves as the basis for describing the temporal picture of atomic photoionization processes [
17,
18,
19,
20,
21,
22,
23,
24,
25]. Equation (
1) in this case needs not to be modified to exclude 
 as the problem of the interference with the unscattered wave does not exist in the case of photoionization. The scattering amplitude 
 for this process must be replaced in Equation (
1) by the photoionization amplitude 
, where 
 is the photon energy
      
The dipole selection rules in photoionization of 
l-states of atom A lead to emission into the continuum of the pair of electronic spherical waves 
 and 
, propagating in the potential field of the atomic residue A
 with the phase shifts 
 and 
, correspondingly, where 
k is the linear photoelectron momentum. The function 
, therefore, is a linear combination of these spherical functions, the coefficients of which are determined by the corresponding dipole matrix elements 
. The energy derivative of the function (
1) implicitly includes the derivatives of both phase shifts 
 and matrix elements 
. The prime sign here and further denotes differentiation with respect to the electron kinetic energy 
E.
The time delay (
4) at some electron emission angles 
 was studied in the series of works on 
photoionization [
19,
20,
21,
22,
23,
24]. To the best of our knowledge, the angular dependence of the time delay in 
elastic electron scattering (
1) has received no attention so far. Our goal in this article is to close somewhat the gap in the area of investigation of the angular time delay in electron scattering (
1) by spherical targets.
We will see further that when only one scattering phase is different from zero in the scattering amplitude (
2), the angular time delay (
1) does not depend on the scattering angle. Here, we analyze the scattering amplitude 
 containing two Legendre polynomials only, i.e., we will consider model targets, in which, as in the case of the dipole photoelectric effect, only one pair of phase shifts is different from zero.
In 
Section 2, the angle dependence of the angular time delays 
 for some fixed electron momenta 
k is investigated. In 
Section 3, the time delay is studied as a function of 
k for some fixed polar angles 
 of the scattering of an incident plane wave train. Finally, the function 
 is averaged over the distance of the order of the de Broglie wavelength, and the 
average angular time delay is obtained in 
Section 4.
  2. Angular -Dependence of the Function 
The argument of the amplitude 
 is determined by the ratio of the imaginary part of the function (
2) 
 to its real part 
      whereas the angular time delay (
1) is described by the general expression
      
Here, and everywhere below, we use the atomic system of units. Let us first consider the case when all the phase shifts in (
2), with the exception of 
, are equal to zero. In this case,
      
It is seen that the angular time delay does not depend on the scattering angle 
 and it is equal to half of the EWS-partial time delay (
3).
Suppose that only two scattering phases 
 and 
 are nonzero. In this case, the scattering amplitude and its argument are represented as
      
Differentiating the argument of the scattering amplitude (
8), we obtain the expression for the time delay
      
      as a function of both scattering angle 
 and electron momentum 
.
Repeating the calculations similar to those in formulae (
8), we obtain the expression for the time delay in the case of nonzero phases 
 and 
It is easy to demonstrate that when only two scattering phases 
 and 
 are nonzero in the electron scattering amplitude (
2), the angular delay time (
5) is determined by the following combination of the Legendre polynomials 
 and 
:
Explicit expressions for the time delays for selected nonzero scattering phase pairs (
11) are given in [
26], where the results of the calculations of the 
- and 
E-dependencies of the corresponding angular time delays are also given. We use both hard-sphere and delta-shell potentials as potential functions for the model targets. For these potentials, the analytical expressions for the scattering phases are known. When an electron is scattered by the model target in the form of an ideally repulsive solid sphere of radius 
R, the phase shifts of the electron are determined by the formula [
27]
      
      where 
 and 
 are the spherical Bessel functions.
The scattering phase shifts of an electron for another model target taken in the form of an attractive delta-shell (delta-shell potential well [
28]) are determined by the expression (see Equation (
10) in [
29])
      
      where the variable 
. The parameter 
 in (
13) is the jump of the logarithmic derivative of the electron wave functions at the point 
 where the delta-shell potential 
 is infinitely negative. In the numerical calculations of phase shifts (
12) and (
13), the radii 
R and the parameter 
 have the same values as those used in our article [
29], where the EWS time delay of slow electrons scattered by a C
 cage was calculated.
Figure 1 shows the results of the calculation by formula (
9) of the angular time delay 
 as a function of the scattering angle 
 for some fixed electron momenta 
k. The left panel corresponds to the scattering on the solid sphere. The right panel corresponds to the delta-shell target. The angular time delays in these figures are given in atomic units. The atomic unit of time is equal to 24.2 attoseconds. Despite the different scales of the graphs on both panels, they show qualitatively similar behavior. The only exceptions are for the curves at 
. The graph of the angular dependence for the hard-sphere is almost a straight line passing from a positive to a negative half-plane at the angle of about 60
, whereas on the right panel, this curve almost coincides with the x-axis. According to both panels, at low electron energies (
 and 0.34), the time delay of the scattering packet is negative at all the scattering angles. The rest of the curves (except the hard-sphere target at 
) are alternating for both targets. At the momenta 
 and 
, the time delays on the right panel reach its maximum (∼298 atomic units (au) at 
 in the first case and ∼140 au at the same angle in the second one). The appearance of these sharp peaks in the curves in 
Figure 1 is due to the almost vanishing of the denominator in the expression (
9). The curves at 
 and 
 on the left panel cross the x-axis into the positive half-plane in the region of 90
, forming a peak with a height of ~30 atomic units.
 Figure 2 depicts the curves corresponding to the pair of polynomials 
 and 
. We see here the results of the calculation with formula (
10) of the angular time delay 
 as a function of the scattering angle 
. As the sum of the orbital moments (indices of the Legendre polynomials) is an even number, the curves 
 in 
Figure 2 are symmetric relative to the angle 
. The curves on the left panel, except for the curve at 
, lie entirely in the lower half-plane. The situation is quite different when the wave packet scatters by the delta-shell target. The behavior of the curve at 
 on the right panel is particularly interesting. This curve lies entirely in the positive half-plane, which allows it to be depicted in polar coordinates (see the inset in the right panel). The 3D-picture of the function 
 is a figure of rotation of this curve around the polar axis z, along which the incident plane wave train hits the target. The “wings of the star” shown there correspond to the polar scattering angles 
 and 123
. The qualitative similarity of the curves on both panels of 
Figure 2 is obvious.
 Note the similarity of the curves in 
Figure 2 and the angular spectra in 
Figure 1a,b of the article in [
10] (devoted to the study of angular resolved time delays in photoemission from different atomic sub-shells of noble gases). A direct comparison of the function 
 for the processes of photoionization and elastic scattering cannot be conducted. An exclusion is the case when the dipole matrix element of photo-transitions varies slightly with the radiation frequency, and their derivatives with respect to the photon energy are negligible. Nevertheless, photoelectron spectra are similar to the scattering spectra in that they are symmetric relative to the angle 
. Qualitative behavior of the scattering spectrum on the delta-shell at 
 in 
Figure 2 and the photoelectron spectrum in panel (a) of 
Figure 1 is similar. The same is to be for the curves at 
 in 
Figure 1 and those in panel (b) of 
Figure 1 in [
10].
Summarizing, we note that according to 
Figure 1 and 
Figure 2, the angular 
-dependencies of the function 
 are represented by nontrivial rapidly oscillating curves lying at low electron energies mainly in the negative half-plane. The situation changes with increasing the electron energy where the dependencies become smooth.
  3. -Dependence of Function 
We now investigate the angular time delay 
 as a function of the electron energy 
E for some fixed values of polar angles 
. The calculation results by formulas (
9) and (
10) are shown in 
Figure 3.
All curves in this figure tend to infinity at small electron momenta. The reason for this is that the scattering phase shift in short-range potentials must follow the Wigner threshold law 
 [
30]. In the case of 
s-phase shift, we have 
. The time delay 
 and 
, that contain the derivative of the 
s-phase shift, for 
 tends to infinity: 
. For the orbital moments 
 the derivative of the phase shifts does vanish at the threshold as 
.
The left column of the figures corresponds to the electron scattering by the hard-sphere potential. The figures in the right column correspond to scattering by the delta-shell potential. In the upper right panel of 
Figure 3, the curves practically coincide with each other at small scattering angles 
, up to the angle of 45
. The graphs corresponding to the angles of 135
 and 180
 have alternating signs, and they are characterized by the peaks in both positive and negative half-planes of the coordinate system. We see a qualitatively similar picture in the lower panel of this column where the curves for 
 are presented. The presence of the derivative of the 
s-phase shift in formula (
10) also leads this function to infinity at small electron energies. The curves for angles 30
 and 180
 almost coincide in this figure. The curve at 
 is characterized by the maximum negative amplitude of oscillations. In the lower-left panel of 
Figure 3, we observe strong resonance behavior of all curves, except for the one at 
 and energy 
 atomic units.
In the second and third sections, we limited ourselves to the specific examples of two nonzero phases in the expansion of the wave function of a scattered electron (
2) into partial waves. It is very difficult to interpret rapidly oscillating dependence of the time delays upon the energy 
E and scattering angle 
 even for this simple example. An increase in the number of included essential scattering phases significantly affects the picture of the angular time delays. The increase makes the time delays rapidly oscillating when they are averaged over the energy of incident electrons. As a consequence, the scattering angle becomes inevitable to make the angular time delay 
 observable in an experiment.
  4. Average Time Delay of Scattering Process
The average angular time delay 
 is obtained from (
1) by averaging over the energy spectrum of the incident wave packet, as well as over the directions weighted by the differential cross section 
. This averaging is reduced to the calculation of the integral of the product 
 over all angles of electron scattering by the target and division of the obtained result by the total cross section of elastic electron scattering 
. The calculation of the integral is complicated by the fact that, according to (
1), the function 
 is not defined at 
. It was shown in [
31] that the contribution to the integral from the forward scattering of an electron is determined by the real part of the scattering amplitude at zero angles. As a result of such averaging, Nussenzweig [
31,
32,
33] obtained the expression
      
The second term on the left-hand side of Equation (
14) eliminates the contribution of the forward scattering into the average angular time delay. Thus, the average time delay for the plane wave train 
 is a linear combination of the EWS time delays 
 (
3). The results of the calculation of the function 
 (
14) in the case of electrons scattered by the hard-sphere target are shown in 
Figure 4.
Figure 4 also shows the dependencies calculated under the assumption that the statistical weight of 
 in the sum (
14) is not equal to 
. Instead, it is the ratio of the electron elastic scattering partial cross section 
 to the total cross section 
. For more information about this assumption see, for example, Equation (
10) in [
10] or Equation (
8) in [
29]. The deep peak of the curve corresponding to the combination of the Legendre polynomials 
 and 
 is due to the resonant behavior of curves at 
 au in 
Figure 3.