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During the previous reporting period much progress has been made developing the PALS research
project. Graduate student Brian Wieland has been constructing, testing, and optimizing the
experimental setup in preparation for two upcoming programs: The first involves validating the
experimental apparatus' ability to accurately reproduce measurements of well-known positron lifetimes
in high-purity samples using a radioactive 22Na source. The second is a feasibility study of the
Accelerator-based Gamma-induced Positron Annihilation Spectroscopy (AG-PAS) technique to
perform the same lifetime measurements using a 2MeV Van de Graaf accelerator. These studies will
pave the way for future work using PALS as a nondestructive method for assessing volume defect
densities in high-Z materials.
wherec is the speed of light. The rise time of the PMT signal was measured using a fast oscilloscope
and found to be ~2.5ns. Note that this is ~50% worse than its 1.6ns specification. Using the measured
rise time yields a calculation of lcable = 38.6cm. A range of cable lengths between 20 and 50cm (in
~1cm increments) were constructed and systematically used in the study. Note that for each cable
length tested, the CFD time-walk was checked, and adjusted if necessary, according to the CFD
manual. For a given HV, a minimum in the FWHM of t was observed over a fairly broad range of
cable lengths--between 25 and 40cm—for both PMTs. To summarize, the optimization study yielded
a ~20% improvement in timing resolution, but did not achieve the desired level of 300 to 350ps (or
better) FWHM. A sample distribution of the timing resolution is shown in Figure 2.
Another important aspect of the experimental setup that requires quantification is the energy
resolution of the detectors as well as their ability to produce the expected energy spectra from various
radioactive sources. Figure 3 displays the energy spectra from a 22Na source for both the fast plastic
and BaF2 detectors. Both distributions show the expected spectra albeit with fairly poor energy
resolution. The BaF2 spectrum clearly shows the two expected photopeaks at 511 and 1275keV, and
the fast plastic spectrum clearly shows the expected Compton edges at 340 and 1068keV. The very
narrow peaks at the low energy end of each spectra are thought to be the single escape peaks since
their location and size are very sensitive to collimation of the source as well as the source/detector
geometry (that is, how far the source is from the scintillator). The energy resolution of the detectors
was determined using BaF2 and a 137Cs source--which produces a single 662keV gamma. Figure 4
shows a typical energy resolution plot for the Start PMT. The Start and Stop PMTs give 27.5% and
35.6% energy resolution respectively. This is far from the expected 7.2% specification and could be
the result of a degraded photocathode and dynodes from extended high rate use at higher than
necessary HV.
Figure 3: Start PMT energy spectra from 22Na. Blue data is from the
fast plastic scintillator. Red data is from the BaF2 scintillator. The total
events in each spectrum are normalized to each other.