Thallium Bromide as an Alternative Material for Room-Temperature Gamma-Ray Spectroscopy and Imaging.

Abstract

Thallium bromide is an attractive material for room-temperature gamma-ray spectroscopy and imaging because of its high atomic number (Tl: 81, Br: 35), high density (7.56 g/cm^3), and a wide bandgap (2.68 eV). In this work, 5 mm thick TlBr detectors achieved 0.94% FWHM at 662 keV for all single-pixel events and 0.72% FWHM at 662 keV from the best pixel and depth using three-dimensional position sensing technology. However, these results were limited to stable operation at -20 C. After days to months of room-temperature operation, ionic conduction caused these devices to fail. Depth-dependent signal analysis was used to isolate room-temperature degradation effects to within 0.5 mm of the anode surface. This was verified by refabricating the detectors after complete failure at room temperature; after refabrication, similar performance and functionality was recovered.

As part of this work, the improvement in electron drift velocity and energy resolution during conditioning at -20 C was quantified. A new method was developed to measure the impurity concentration without changing the gamma ray measurement setup. The new method was used to show that detector conditioning was likely the result of charged impurities drifting out of the active volume. This space charge reduction then caused a more stable and uniform electric field. Additionally, new algorithms were developed to remove hole contributions in high-hole-mobility detectors to improve depth reconstruction. These algorithms improved the depth reconstruction (accuracy) without degrading the depth uncertainty (precision). Finally, spectroscopic and imaging performance of new 11~x~11 pixelated-anode TlBr detectors was characterized. The larger detectors were used to show that energy resolution can be improved by identifying photopeak events from their Tl characteristic x-rays.