Multi-Ion Clock
Our main research goal is the implementation of a multi-ion
clock to provide an improved stability for ion-clock systems.
Currently we are seeking to implement clock operation over a small
number of ions with N on the order of 10. Although this may seem
only a modest improvement over a single ion system, it would still
improve integration time by a factor of N.
The challenge for clock operation on multiple ions concerns
inhomogeneous broadening. For a single ion, various clock
shifts can be well calibrated and/or averaged away. For
many ions, these effects can distort the line-shape and give
a frequency shift that depends non-trivially on both the
distribution of individual shifts across the ion crystal,
and the interrogation time. As the interrogation time
increases, shifts are better resolved, which increases
line-shape distortion and hence the resulting clock shift.
Provided the broadening is much smaller than the width of
the individual line-shape function, the shift is linear in
the skewness of the distribution and cubic in both the width
of the distribution and the interrogation time. The cubic
dependence on the distribution compromises shift
cancellation through hyperfine averaging.
The key factors affecting inhomogeneous broadening are:
Magnetic field gradients: Spatial inhomogeneity will
result in a differential shift between ions. Fortunately
lutetium has one of the lowest field dependences amongst all
clock candidates. At a typical operating field of 0.1 mT,
the maximum sensitivity of any single transition involved in
clock operation is about 1.4 kHz/G. For a string of ions
occupying a 50 μm length would then have a maximum
differential shift of 1 Hz for a gradient of 1.4 mT/m. This
is rather trivial to achieve and, moreover, the resulting
distribution would be symmetric.
AC magnetic fields: Fields driven by rf currents in the
electrodes have a spatial variation. However for a
well-designed linear Paul trap, we would expect this to be
fairly uniform along the trap axis. Moreover the shift
itself can be expected to be rather small at least for the macroscopic traps we currently use.
Quadrupole shifts: For the macroscopic traps we currently
use, the quadrupole shift from the trap confinement will be
very homogeneous over a small linear chain of ions. Hence
the only significant broadening will be from electric field
gradients generated from neighboring ions. These effects
can be suppressed by having the magnetic field at a specific
angle to the crystal. This can be tested using microwave
spectroscopy on the 3D1 levels and we
expect to suppress this shift to better than
10-19 under realistic conditions.