1. IntroductionPhotodetachment process plays an important role in investigating the structure of negative ions in atomic or molecular physics. As is well known the external field or environment can modulate the photodetachment process of negative ion. It has been observed that the photodetachment cross section of H− ion in a strong static electric field displayed a ripple structure.[1] In order to explain this phenomenon, many theoretical studies have been carried out using both the quantum mechanical method and the semiclassical method.[2–7] For example, in 1988, Rau and Wong used the “Frame transformation theory” to calculate the photodetachment cross section in the coordinate representation.[2] The effect of the electric field appeared as a modulating factor given by a derivative of an Airy function. At the same time, Du and Delos adopted a quantum method involving a momentum space wave function and stationary phase approximation and derived a simple formula for calculating the photodetachment cross section of this system.[3] Later, Du and Delos used the semiclassical closed orbit theory to explain the oscillatory structure in the photodetachment cross section and found their result accords very well with the quantum mechanical result.[4–7] Since the closed orbit theory provides a clear physical picture description for the photodetachment of H− ion in the electric field, many researchers have developed this theory to study the photodetachment of H− ion in other external fields or different environments, such as in parallel or crossed electric and magnetic fields, near an elastic or metal surface, in different microcavities, etc.[8–22] In these previous studies, the external fields or environment remain unchanged. As to the photodetachment of H− ion in the changing external field or environment, the researches are relatively few. In 1999, Yang et al. studied the photodtachment of H− ion in a space-dependent gradient electric field.[23] Later, Zhao et al. calculated the photodetachment cross section of H− ion in a harmonic potential.[24] Recently, Yang and Robicheaux have developed the closed orbit theory from the static electric field into the time-dependent electric field. They studied the photodetachment of H− and F− ion in a time-dependent electric field.[25,26] On this basis,we have studied the photodetachment of H− ion in a time-dependent gradient electric field and oscillating electric field.[27,28] However, it is unknown what will happen for the photodetachment of H− ion in an electric field varying with both space and time.
In the present work, the photodetachment dynamics of the H− ion in a harmonic potential plus an oscillating time-dependent electric field is studied. We put forward an analytical formula for calculating the photodetachment cross section of this system. It is found that the photodetachment cross section depends sensitively on the strength of the oscillating electric field and the frequency in the harmonic potential and the oscillating electric field (the frequency of the harmonic potential and the frequency of the oscillating electric field are the same in the paper, unless otherwise stated.). Since the harmonic potential corresponds to a space-dependent electric field, thus our study presents an intuitive understanding of the photodetachment dynamics of negative ions in the electric field from a space and time dependent viewpoint.
In the following section, we give the Hamiltonian and obtain the classical motion equations for the detached electrons in the harmonic potential plus the oscillating electric field. Then we search out the closed orbits for the detached electrons. In Section 3, we put forward an analytical formula for calculating the photodetachment cross section of this system. The influences of the oscillating electric field strength and the variation of the frequency in the harmonic potential and the oscillating electric field on the photodetachment cross section are calculated and discussed in Section 4. In Section 5 a short summary of this paper is presented. Atomic units (a.u.) are used unless indicated otherwise.
2. Hamiltonian and the closed orbit of the detached electronConsidering that an H− ion is placed in a harmonic potential
plus a time-dependent oscillating electric field
, where ω is the frequency of the harmonic potential and the oscillating electric field, F0 is the electric field strength. The laser field for the photodetachment of the H− ion has the following form[25]
where
![](cpb_26_10_103202/cpb_26_10_103202_ieqn3.gif)
,
![](cpb_26_10_103202/cpb_26_10_103202_ieqn4.gif)
, and
![](cpb_26_10_103202/cpb_26_10_103202_ieqn5.gif)
are the laser field parameters, with
![](cpb_26_10_103202/cpb_26_10_103202_ieqn6.gif)
, and
![](cpb_26_10_103202/cpb_26_10_103202_ieqn7.gif)
indicating the time when the laser light is turned on and off, respectively,and
![](cpb_26_10_103202/cpb_26_10_103202_ieqn8.gif)
controlling how fast the laser field is turned on and off.
[27] In this work, we choose
![](cpb_26_10_103202/cpb_26_10_103202_ieqn9.gif)
, and
![](cpb_26_10_103202/cpb_26_10_103202_ieqn10.gif)
.
Assuming that the laser field and the oscillating electric field both point along the z axis. Then the Hamiltonian governing the motion of the detached electron in the harmonic potential plus the oscillating electric field has the following form:
Here pt is a conjugate momentum relating to the classical dynamical variable t,
is the binding potential and can be neglected after the electron has been far from the hydrogen atom.
Since the Hamiltonian is related to time t, we introduce an additional evolution time τ to describe the electron movement in the harmonic potential plus the oscillating electric field,
. Here
denotes the initial outgoing time of the electron trajectory and t is the real time. By solving the time-dependent Hamiltonian canonical equations with the initial conditions:
,
,
,
, we obtain the motion equations of detached electron as follows:
where
![](cpb_26_10_103202/cpb_26_10_103202_ieqn18.gif)
is the initial momentum of detached electron,
θ![](cpb_26_10_103202/cpb_26_10_103202_ieqn19.gif)
denotes the outgoing angle between the initial momentum with the +
z axis,
A and
φ0 are the integration constants, which can be determined by the initial conditions of the detached electron:
From Eq. (3), we find that the electron motion along the z axis is a cyclotron one, and the motion perpendicular to the z axis is a linear motion. Then only the electron emitted along the z axis can be drawn back to the origin to form a closed orbit. Therefore, the initial outgoing angle of the closed orbit of electron in the harmonic potential plus the oscillating electric field is
or
.
Let
, then we will obtain
![](cpb_26_10_103202/cpb_26_10_103202_eqn6.gif) | |
By solving the above equation, we can obtain the initial time
and the returning time t of each closed orbit. Some typical closed orbits are shown in Fig. 1. Figure 1(a) shows the electron emitted along the +z direction, due to the influences of the harmonic potential and the electric field force, after a period of time it will return back to the origin. We call this kind of closed orbit the up orbit. Figure 1(b) shows the electron emitted along the −z axis with the outgoing angle
, after some time, it reaches the lowest point, and then pulls back to the origin by the harmonic potential and the electric field force. This kind of closed orbit is called the down orbit. Figure 1(c) can be considered as a combination of the up and down closed orbit, which is called the up–down orbit. Figure 1(d) shows an orbit similar to the up–down orbit, but in reverse order. We call it the down–up orbit. The other two closed orbits can be analyzed in the same manner. Figures 1(e) and 1(f) are called the up–down–up orbit, and down–up–down orbit, respectively.
3. Derivation of the time-dependent photodetachment cross sectionAccording to the closed orbit theory,[7] the external field can modulate the photodetachment process of the H− ion by returning back an outgoing wave to the source region, where the initial bound state of H− ion is localized. If the harmonic potential and the oscillating electric field are strong enough that the electron can be driven back to the origin, oscillatory structures may appear in the photodetachment cross section. Each closed orbit of the detached electron contributes a sinusoidal term in the total photodetachment cross section. In contrast to the photodetachment of the H− ion in the static electric field, where the photodetachment cross section is time-independent. However, in the time-dependent oscillating electric field, the returning electron orbit oscillates with time, which makes the photodetachment cross section change with time t. It has been shown that the time-dependent photodetachment cross section can be divided into two parts[27]
where
![](cpb_26_10_103202/cpb_26_10_103202_ieqn25.gif)
is a smooth background term, which is only related to the laser field,
![](cpb_26_10_103202/cpb_26_10_103202_ieqn26.gif)
, where
![](cpb_26_10_103202/cpb_26_10_103202_ieqn27.gif)
is the photodetachment cross section of H
![](cpb_26_10_103202/cpb_26_10_103202_ieqn28.gif)
ion in the free space.
[7] Here
c is the speed of light;
B = 0.31552;
![](cpb_26_10_103202/cpb_26_10_103202_ieqn29.gif)
is the photon energy, with
E being the energy of detached electron and
![](cpb_26_10_103202/cpb_26_10_103202_ieqn30.gif)
being the binding energy of the H
− ion and
![](cpb_26_10_103202/cpb_26_10_103202_ieqn31.gif)
;
![](cpb_26_10_103202/cpb_26_10_103202_ieqn32.gif)
denotes the oscillating cross section, corresponding to the contribution of the returning electron wave:
Here
D is the dipole operator and
D=
Z for the
z-polarized laser light;
![](cpb_26_10_103202/cpb_26_10_103202_ieqn33.gif)
is the initial bound state wave function of the H
− ion,
![](cpb_26_10_103202/cpb_26_10_103202_ieqn34.gif)
,
![](cpb_26_10_103202/cpb_26_10_103202_ieqn35.gif)
denotes the returning electron wave function:
Hear,
![](cpb_26_10_103202/cpb_26_10_103202_ieqn36.gif)
is the returning wave corresponding to the
v-th closed orbit of the detached electron, and the sum includes all the closed orbits of electron:
Here,
is a coefficient:
![](cpb_26_10_103202/cpb_26_10_103202_ieqn38.gif)
is the harmonic function, in this work, we choose
l=1,
m=0;
R is the radius of a small spherical surface around the negative ion, R ≈10 a.u;
Av and
Sv are the amplitude and action along the
v-th trajectory;
λv is the Maslov index characterizing the geometrical properties of the
v-th trajectory, which can be calculated by counting the number of the singular points, including returning points, caustics, and foci, etc.
[27]The amplitude Av is the ratio of the square root of Jacobian at time
to that at τ = 0, i.e.,
In the cylindrical coordinates,
![](cpb_26_10_103202/cpb_26_10_103202_ieqn40.gif)
is defined as
[24]
Using the classical motion equation for the detached electron in the harmonic potential plus the oscillating electric field (Eq. (
3)), we obtain
The classical action Sv along the v-th closed orbit can be calculated from
Due to the influences of the harmonic potential and the electric field force, the electron will return back to the source region after a period of time. Around the source region (usually a few atomic units in size,
, we find that the influences of the electric field potential and the harmonic potential
on the detached electron are small. Therefore, the returning wave function behaves like a plane wave:
where
![](cpb_26_10_103202/cpb_26_10_103202_ieqn43.gif)
is a matching factor, which is given by
with
![](cpb_26_10_103202/cpb_26_10_103202_ieqn44.gif)
being a redefined action function
[24] ![](cpb_26_10_103202/cpb_26_10_103202_ieqn45.gif)
.
The symbol “±” in the exponent in Eq. (14) is determined by the direction of the returning wave: if the electron wave returns along the −z axis, we choose “−” in the phase factor; however, for the electron wave returns along the +z axis, we use symbol “+”. The
in Eq. (14) is the returning electron momentum.
Substituting
into Eq. (14), and carrying out the overlap integral in Eq. (8), we obtain the oscillating term in the photodetachment cross section as follows:
where
gv is a factor. If the outgoing and returning directions for the electron orbit are the same,
![](cpb_26_10_103202/cpb_26_10_103202_ieqn48.gif)
; otherwise
![](cpb_26_10_103202/cpb_26_10_103202_ieqn49.gif)
.
[26]By combining Eq. (16) and Eq. (7), we o the total time-dependent photodetachment cross section of H− ion in the harmonic potential plus the oscillating electric filed:
4. Results and discussionUsing Eq. (17), we calculate the time-dependent photodetachment cross section of an H− ion in the harmonic potential plus the oscillating electric field. In this work, we choose the photon energy
, the initial outgoing time
and the returning time t which are localized in the region [−3.14 ps, +3.14 ps]. Firstly, we keep the frequency in the harmonic potential and the oscillating electric field unchanged,
a.u., then we study the influence of the oscillating electric field strength on the photodetachment cross section.
In Fig. 2, we discuss the photodetachment of this system with a relatively weak electric field strength,
. Through numerical calculation, we find only two closed orbits of the detached electron existing: one is the down closed orbit and the other is the down–up closed orbit as shown in Fig. 1. The t–
curves for these two orbits are shown in Fig. 2(a). From this figure, we can obtain the initial outgoing time
and the returning time t for the down and down–up closed orbits. Figure 2(b) shows the photodetachment cross section under this condition. Oscillatory structure appears in the cross section due to the effect of interference between the returning electron wave and the initial outgoing wave. However, the oscillating amplitude is relatively small and the oscillatory structure is restricted only in a small interval. The reason can be explained as follows. If the oscillating electric field strength F0 is very weak, the electric field force acting on the detached electron is very small compared with the effect of the harmonic potential. If the electron is emitted along the +z axis, the electric field force cannot return it back to the origin. Thus the up closed orbit does not exist. In addition, the variation of the photodetachment cross section with time is not obvious and the time-dependent effect on the cross section can be neglected.
As the strength of the oscillating electric field increases, its influence on the detached electron becomes strong. Except the down and down–up closed orbits, the up closed orbit also appears. Figure 3(a) shows the
–t curves for these three orbits with the electric field strength
. From this plot, we find for the down and down–up closed orbits, the initial outgoing time
for the detached electron is negative; however, for the up closed orbit,
can be negative or positive. In addition, the returning time for the up closed orbit is only localized in a small interval:
. The corresponding photodetachment cross section with the electric field strength
is shown in Fig. 3(b). It is found that the oscillatory structure in the photodetachment cross section turns complex and the time-dependent effect on the cross section becomes obvious compared with the scenario in Fig. 2(b). However, the oscillation in the cross section is mainly caused by the down and down–up closed orbit, the contribution of the up closed orbit to the photodetachment cross section is very small and can be neglected.
As the oscillating electric field strength further increases, there are still three different types of closed orbits as shown in Fig. 3(a). But the contribution of the up closed orbit to the cross section turns apparent and the oscillatory structure in the photodetachment cross section becomes much more complicated. Both the oscillating region and the oscillating amplitude are enlarged. For example, in Fig. 4(a), the electric field strength
. We find that the oscillating structure in the photodetachment cross section is localized in the region
; however, when the electric field strength increases to
as shown in Fig. 4(c), the oscillating region increases
. The reason can be analyzed as follows: with the increase of electric field strength, the electric field force acting on the detached electron becomes stronger, which makes the period of the closed orbit shorter. From Eq. (12), we find that the amplitude for each closed orbit becomes increased. According to the closed orbit theory, the oscillation in the photodetachment cross section is caused by the interference between the returning electron wave and the initial outgoing electron wave. After the electron is emitted from the origin, the strong electric field force will return the electron back in a small period of time, which causes the interference effect in the photodetachment cross section to become stronger. Therefore, the oscillatory structure in the time-dependent cross section goes complicated with the increase of electric field strength.
Next, we keep the electric field strength
unchanged, then we discuss the variation of the photodetachment cross section with frequency ω in the harmonic potential and the oscillating electric field. The result is shown in Fig. 5. Figure 5(a) shows the photodetachment cross section with frequency
a.u. Under this condition, the influences of the harmonic potential and the oscillating electric field on the detached electron are small, only the down and the down–up closed orbits exist. The oscillating amplitude in the photodetachment cross section is relatively small. With the increase of the frequency in the harmonic potential and the oscillating electric field, the number of the closed orbits increases. Figure 5(b) shows the photodetachment cross section with frequency
a.u. There are three different types of closed orbits of detached electron, namely, the up orbit, down orbit, and the down–up orbit, which makes the oscillatory structure in the photodetachment cross section complex. As the frequency increases to
a.u., the number of the closed orbits of detached electron increases to 4. Except the up, down, and the down–up orbit, the up–down orbit can also exist. The total photodetachment cross section is shown in Fig. 5(c). The oscillatory structure in the photodetachment cross section goes further complex. Figure 5(d) shows the photodetachment cross section with frequency
a.u. Under this condition, the fast oscillation in the harmonic potential and the oscillating electric field makes the number of the closed orbits increased to 7. We can clearly see that the oscillatory structures become much more complicated, and the oscillating amplitude in the cross section increases greatly. The reason is as follows. With the increase of the frequency in the harmonic potential and the oscillating electric field, the number of the closed orbits of the detached electron increases. As we stated above, the interference between the returning electron wave and the initial outgoing electron wave leads to the oscillatory structure in the photodetachment cross section: the more the number of the closed orbits, the more the returning waves that return back to the atom; therefore, their interference effect will become strong, which makes the oscillation in the cross section complicated.
Finally, in order to see the relation of each closed orbit to the photodetachment cross section, we remove the background term in Eq. (17) and only calculate the oscillating part
in the photodetachment cross section. The electric field strength and the frequency in the harmonic potential and the oscillating electric field are the same as those given in Fig. 5(d). Under this circumstance, there are 7 closed orbits of the detached electron: the up orbit, down orbit, up–down orbit, down–up orbit, up–down–up orbit, down–up–down orbit, and up–down–up–down orbit. Figure 6(a) shows the total oscillating cross section caused by these 7 closed orbits of the detached electron. Figures 6(b)–6(h) show the oscillating cross sections caused by the corresponding type of closed orbit respectively. By comparing the above figures, we can see that the oscillations in the cross section, caused by the up and down closed orbits play the significant roles, followed by the contribution of the up–down and down–up orbits. The oscillations in the cross section, caused by the other three closed orbits, are relatively small. The reason is as follows. Because the periods of the up orbit and down orbit are relatively shorter than the periods of the other orbits, from Eq. (12) we can see that the values of amplitude factor A for these two orbits are large, thus their contributions to the cross section are significant. However, for the other closed orbits, their periods are longer, which makes the amplitude factor become smaller, as a consequence, the oscillating amplitudes caused by these orbits are negligible compared with those by the up and down orbits.
5. ConclusionsAccording to the time-dependent closed orbit theory, we study the influences of the harmonic potential and the oscillating electric field on the photodetachment cross section of the H− ion. An analytical formula for calculating the photodetachment cross section of this system is put forward. It is found that when the oscillating electric field strength is very weak, the oscillatory structure in the photodetachment cross section is nearly invisible. However, if the electric field is strong, the photodetachment cross section oscillation turns complicated. On the other hand, we notice that when the frequency in the harmonic potential and the oscillating electric field is small, only two closed orbits of detached electron exist, which makes the interference effect in the photodetachment cross section less complex. With the increase of the frequency in the harmonic potential and the oscillating electric field, the number of closed orbits of detached electron increases, and the oscillatory structure in the photodetachment cross section goes much more complex. In addition, the relation of each closed orbit to oscillating photodetachment cross section is analyzed qualitatively. In this work, we only consider the case that the frequencies of the oscillating electric field and the harmonic potential are equal. When the frequency in the oscillating electric field is unequal to the frequency in the harmonic potential, the motion equations of the detached electron and the photodetachment cross section will be changed. However, the method we used in this paper is still suitable. Our study provides a clear and intuitive picture for the photodetachment dynamics of H− ion driven by a harmonic potential plus a time-dependent oscillating electric field. We hope that our work can guide the future experimental research of the photodetachment dynamics in the space and time varying electric field.