Electromagnetic Traps For Charged and Neutral Particles: Olfgang AUL
Electromagnetic Traps For Charged and Neutral Particles: Olfgang AUL
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one assumes that all atoms show exactly the same statistical behaviour if one
attributes the result to the single atom. On a trapped single atom, however,
one can observe its interaction with a radiation field and its own statistical
behaviour alone.
The idea of building traps grew out of molecular beam physics, mass
spectrometry and particle accelerator physics I was involved in during the
first decade of my career as a physicist more than 30 years ago. In these
years (1950 - 55) we had learned that plane electric and magnetic multipole
fields are able to focus particles in two dimensions acting on the magnetic or
electric dipole moment of the particles. Lenses for atomic and molecular
beams [1,2,3] were conceived and realized improving considerably the
molecular beam method for spectroscopy or for state selection. The lenses
found application as well to the ammonia as to the hydrogen maser [4].
The question What happens if one injects charged particles, ions or
electrons, in such multipole fields led to the development of the linear
quadrupole mass spectrometer. It employs not only the focusing and defocusing forces of a high frequency electric quadrupole field acting on ions
but also exploits the stability properties of their equations of motion in
analogy to the principle of strong focusing for accelerators which had just
been conceived.
If one extends the rules of two-dimensional focusing to three dimensions
one posseses all ingredients for particle traps.
As already mentioned the physics or the particle dynamics in such focusing devices is very closely related to that of accelerators or storage rings for
nuclear or particle physics. In fact, multipole fields were used in molecular
beam physics first. But the two fields have complementary goals: the storage
of particles, even of a single one, of extremely low energy down to the microelectron volt region on the one side, and of as many as possible of extremely high energy on the other. Today we will deal with the low energy part. At
first I will talk about the physics of dynamic stabilization of ions in two- and
three-dimensional radio frequency quadrupole fields, the quadrupole mass
spectrometer and the ion trap. In a second part I shall report on trapping of
neutral particles with emphasis on an experiment with magnetically stored
neutrons.
As in most cases in physics, especially in experimental physics, the
achievements are not the achievements of a single person, even if he
contributed in posing the problems and the basic ideas in solving them. All
the experiments I am awarded for were done together with research students or young colleagues in mutual inspiration. In particular, I have to
mention H. Friedburg and H. G. Bennewitz, C.H. Schlier and P. Toschek in
the field of molecular beam physics, and in conceiving and realizing the
linear quadrupole spectrometer and the r.f. ion trap H. Steinwedel, O.
Osberghaus and especially the late Erhard Fischer. Later H.P. Reinhard, U.
v. Zahn and F. v. Busch played an important role in developing this field.
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What are the principles of focusing and trapping particles? Particles are
elastically bound to an axis or a coordinate in space if a binding force acts
on them which increases linearly with their distance r
In other words if they move in a parabolic potential
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Figure I. a) Equipotential lines for a plane quadrupole fild, b) the electrodes Structure for the
mass filter.
If one injects ions in the y-direction it is obvious that for a constant voltage
<Do the ions will perform harmonic oscillations in the the x-y-plane but due
to the opposite sign in the field E their amplitude in the z-direction will
increase exponentially. The particles are defocused and will be lost by
hitting the electrodes.
This behaviour can be avoided if the applied voltage is periodic. Due to
the periodic change of the sign of the electric force one gets focusing and
defocusing in both the x- and z-directions alternating in time. If the applied
voltage is given by a dc voltage U plus an r.f. voltage V with the driving
frequency
z
At first sight one expects that the time-dependent term of the force
cancels out in the time average. But this would be true only in a homogenous field. In a periodic inhomogenous field, like the quadrupole field there
is a small average force left, which is always in the direction of the lower
field, in our case toward the center. Therefore, certain conditions exist that
enable the ions to traverse the quadrupole field without hitting the electrodes, i.e. their motion around the y-axis is stable with limited amplitudes
in x- and z-directions. We learned these rules from the theory of the Mathieu
equations, as this type of differential equation is called.
In dimensionless parameters these equations are written
(5)
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Figure 2. The overall stability diagram for the two-dimensional quadrupole field.
0.3
0.23
0.2
t
a
0.1
Figure 3. The lowest region for simultaneous stability in x-and z-direction. All ion masses lie on the
operation line, m1 > m1.
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min
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Figure 5. a) Very first mass spectrum of Rubidium. Mass scanning was achieved by periodic
variation of the driving frequency v. Parameter: u = $, at u = 0.164 85 Rb and 87 Rb are fully
resolved. b) Mass doublet 83Kr - C 6H 11. . Resolving power m/m = 6500 [9].
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Figure 6. a) Schematic view of the ion trap. b) Cross section of the first trap (1955).
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If one brings ions into the trap, which is easily achieved by ionizing inside
a low pressure gas by electrons passing through the volume, they perform
the same forced motions as in the two-dimensional case. The only difference
is that the field in z-direction is stronger by a factor 2. Again a periodic field
is needed for the stabilization of the orbits. If the voltage Q0 = U + Vcos mt
is applied between the caps and the ring electrode the equations of motion
are represented by the same Mathieu functions of eq.(5). The relevant
parameters for the r motion correspond to those in the x-direction in the
plane field case. Only the z parameters are changed by a factor 2.
Accordingly, the region of stability in the a-q-map for the trap has a
different shape as is shown in Fig. 7. Again the mass range of the storable
ions (i.e. ions in the stable region) can be chosen by the slope of the
operation line a/q = 2U/V. Starting with operating parameters in the tip of
the stable region one can trap ions of a single mass number. By lowering the
d.c. voltage one brings the ions near the q-axis where their motions are
much more stable.
For many applications it is necessary to know the frequency spectrum of
the oscillating ions. From mathematics we learn that the motion of the ions
can be described as a slow (secular) oscillation with the fundamental fre-
Figure 7. The lowest region for stability in the ion trap. On the lines inside the stability region /$
and B, resp. are constant.
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Figure 8. Mechanical analogue model for the ion trap with steelball as particle
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appropriate to the potential parameters and the mass of the ball (in our case
a few turns/s) the ball becomes stable, makes small oscillations and can be
kept in position over a long time. Even if one adds a second or a third ball
they stay near the center of the disc. The only condition is that the related
Mathieu parameter q be in the permitted range. I brought the device with
me. It is made out of Plexiglas which allows demonstration of the particle
motions with the overhead projector.
This behaviour gives us a hint of the physics of the dynamic stabilization.
The ions oscillating in the r- and z-directions to first approximation harmonically, behave as if they are moving in a pseudo potential well quadratic
in the coordinates. From their frequencies O, and O, we can calculate the
depth of this well for both directions. It is related to the amplitude V of the
driving voltage and to the parameters a and q. Without any d.c. voltage the
depth is given by Dz = (q/8) V, in the r-direction it is half of this. As in
practice V amounts to a few hundred volts the potential depth is of the
order of 10 Volts. The width of the well is given by the geometric dimensions. The resulting configuration of the pseudo potential [14] is therefore
given by
Cooling process
positions where the repulsive Coulomb force is compensated by the focusing forces in the trap and the energy of the ensemble has a minimum. Figs.
10a, b show such a pattern with 7 ions. Their distance is of the order of a
few micrometers. These observations opened a new field of research [18].
The Ion Trap as Muss Spectrometer
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Figure 10. a) Pseudo crystal of 7 magnesium ions. Particle distance 23 m. b) The same trapped
particles at higher temperature. The crystal has melted [18].
If one applies to the quadrupole trap only a d.c. voltage in such a polarity
that the ions perform stable oscillations in the z-direction with the frequency CO: = , Ix
, ; the ions are unstable in the x-y-plane, since the field is
directed outwards. Applying a magnetic field in the axial direction, the
z-motion remains unchanged but the ions perform a cyclotron motion
in the x-y-plane. It is generated by the Lorentz force F directed towards
the center. This force is partially compensated by the radial electric force
F, = & r. As long as the magnetic force is much larger than the electric one,
stability exists in the r-y-plane as well. No r.f. field is needed. The resulting
rotation frequency calculates to
L
Figure Il. First mass spectrum achieved with the ion trap. Gas: air at 2 . 10 -9 torr [19]
In the last examination I had to pass as a young man I was asked if it would
be possible to confine neutrons in a bottle in order to prove if they are
radioactive. This question, at that time only to be answered with no,
pursued me for many years until I could have had replied: Yes, by means of
a magnetic bottle. It took 30 years until by the development of superconducting magnets its realization became feasible.
Using the example of such a bottle I would like to demonstrate the
principle of confining neutral particles. Again the basis is our early work on
focusing neutral atoms and molecules having a dipole moment by means of
multipole fields making use of their Zeeman or Stark effect to first and
second order [1,2,3]. Both effects can be used for trapping. Until now only
magnetic traps were realized for atoms and neutrons. Particularly, B. Martin, U. Trinks, and K. J. Kgler contributed to their development with great
enthusiasm.
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Figure 12. a) Ideal sextupole field. Dashed: magnetic field lines, dotted: lines of equal magnetic
potential, B = const. b) Linear sextupole made of 6 straight current leads with alternating
current direction.
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with alternating current directions arranged in a hexagon. Such a configuration works as a lense for particles moving along the y-axis.
There are two possibilities to achieve a closed storage volume: a sextupole
sphere and a sextupole torus. We have realized and studied both.
The spherically symmetric field is generated by three ring currents in an
arrangement shown in Fig. 13. The field B increases in all directions with r 2
and has its maximum value B0 at the radius r0 of the sphere. Using superconducting current leads we achieved B0 = 3T in a sphere with a radius of 5 cm.
But due to the low magnetic moment of the neutron = 6 * 10-8 eV/T the
potential depth B o is only 1.8 * 10-7 eV and hence the highest velocity of
storable neutrons is only v max = 6m/s . Due to their stronger moment for Na
atoms these values are 2.2 * 10-4 eV and 37 m/s, respectively.
The main problem with such a closed configuration is the filling process,
especially the cooling inside. However, in 1975 in a test experiment we
succeeded in observing a storage time of 3 s for sodium atoms evaporated
inside the bottle with its Helium cooled walls [25]. But the breakthrough in
confining atoms was achieved by W. D. Phillip and H.J. Metcalf using the
modern technique of Laser cooling [26].
The problem of storing neutrons becomes easier if one uses a linear
sextupole field bent to a closed torus with a radius R as is shown in Fig. 14.
The magnetic field in the torus volume is unchanged B = $Q * ? and has
no component in azimuthal direction. The neutrons move in a circular orbit
with radius Rs if the centrifugal force is compensated by the magnetic force
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focusing have to be replaced by sextupoles and e.g. octupoles for stabilization of the orbits by decapoles.
In the seventies we have designed and constructed such a magnetic
storage ring with a diameter of the orbits of 1 m. The achieved usable field
of 3.5 T permits the confinement of neutrons in the velocity range of 5 - 20
m/s corresponding to a kinetic energy up to 2 * 10-6 eV. The neutrons are
injected tangentially into the ring by a neutron guide with totally reflecting
walls. The inflector can be moved mechanically into the storage volume and
shortly afterwards be withdrawn.
The experimental set up is shown in Fig. 15. A detailed description of the
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storage ring, its theory and performance is given in [27]. In 1978 in a first
experiment we have tested the instrument at the Grenoble high flux reactor. We could observe neutrons stored up to 20 min after injection by
moving a neutron counter through the confined beam after a preset time.
As by the detection process the neutrons are lost, one has to refill the ring
starting a new measurement. But due to the relatively low flux of neutrons
in the acceptable velocity range, their number was too low to make relevant
measurements with it.
In a recent experiment [28] at a new neutron beam with a flux improved
by a factor 40 we could observe neutrons up to 90 min, i.e. roughly 6 times
the decay time of the neutron due to radioactive decay. Fig. 16 shows the
measured profile of the neutron beam circulating inside the magnetic gap.
Measuring carefully the number of stored neutrons as a function of time we
could determine the lifetime to = 877 10 s (Fig. 17).
The analysis of our measurements lets us conclude that the intrinsic
storage time of the ring for neutrons is at least about one day. It shows that
we had understood the relevant problems in its design.
Figure 16. Beam profile of the stored neutrons inside the magnet gap 400 sec after injection.
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Figure 17. Logarithmic decrease of the number of stored neutrons with time.
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Figure 18. Downward shift of the equilibrium center of the neutron orbits due to the weight of
the neutron as function of the magnetic current.
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