Individually,
a helium-4 atom is one of the simplest objects in the universe: two
protons, two neutrons and two electrons. At high temperatures, a
collection of such atoms behaves as the classical ideal gas. At low
temperatures, in liquid form, quantum mechanics comes into play, and
the collective behavior of many helium atoms together is radically
different from that observed in other liquids. The He-4 atoms are
bosons, and so in the right conditions, Bose-Einstein condensation
occurs, creating the superfluid state. Under pressure, the liquid
solidifies, but the crystal formed is, as might be expecte, a little
unusual. It is a quantum crystal, so named because quantum effects
(zero point motion) dominate thermal effects. In fact, the atomic zero
point motion is so large that classically, the solid should melt.
Nonetheless, the solid exists!
In the 1960s and 1970s, several people wondered whether or not a state
analogous to the superfluid might form in the solid state: the supersolid state [ref].
However, no experimental evidence for such a thing was found at that
time. In 2002, John Goodkind at UCSD saw some anomalies in the
transmission of ultrasound through solid helium crystals, and
speculated that they were due to interactions with excitations of
delocalized defects [ref].
In 2004, Eunseong Kim and
Moses Chan
at Pennsylvania State University observed the predicted signature of
the supersolid, a change in the rotational inertia of solid helium away
from the values expected for a classical solid [ref].
These measurements have since been reproduced by several other groups.
However, the interpretation of these results remains controversial.
We are collaborating with the
Goodkind group at UCSD and
Collin Broholm
at Johns Hopkins University to investigate the structural and dynamical
properties of solid He-4 crystals in the relevant temperature and
pressure ranges using neutron scattering. |
We carried out neutron diffraction studies on some He crystals at the
MAPS spectrometer
at the ISIS Facility, Rutherford-Appleton Laboratory, Oxford, UK. This
instrument is equipped with a huge number of detectors (16 square
meters) and so can monitor a number of Bragg peaks simultaneously.
FIG: A 2D layout of the detector banks on MAPS. The black dots and streaks are Bragg reflections from the solid helium
The samples were grown in situ
in a large stainless steel chamber in a dilution refrigerator. Helium
gas was pumped into the cell through a thin capillary and then
liquefied and finally solidified. The crystals were grown using the blocked capillary
technique: helium is pushed in at a high pressure and relatively high
temperature. Eventually, a plug of solid forms in the capillary and the
helium trapped in the sample cell is cooled. This technique usually
results in poor quality crystals, and in fact, in our experiment,
several crystallites were formed.

FIG: Stainless steel sample cell.
Nonetheless, specific Bragg peaks were easily identified from their
characteristic momentum transfer (position in reciprocal space) and the
temperature dependence of these peaks was monitored from 0.14 K to 0.80
K. By looking at the change in intensity of peaks from the same
crystallite, we can extract information on atomic displacements about
their average positions. For helium, the mean square displacement is
very large (approximately one third of the atomic separation) and
should be sensitive to certain types of changes in the local
environment brought about by the appearance of a supersolid conensate.
Over the temperature range studied here, this quantity is temperature
independent.
We can also monitor the evolution of the lattice parameters as a
function of temperature. Making certain assumptions, the temperature
dependence of the lattice parameters can be mapped to the temperature
dependence of the vacancy concentration in the crystal. Together with
data over a higher temperature range obtained from x-ray diffraction
experiments by Fraass, Granfors and Simmons [ref]
our data show that this temperature dependence is clearly exponential
in nature, with an apparent vacancy activation energy of 8.6 K. |