Publications

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The light output, time resolution, pulse shape discrimination (PSD), neutron light output, and interaction position reconstruction of melt-cast small-molecule organic glass bar scintillators were measured. The trans-stilbene organic scintillator detects fast neutrons and gamma rays with high efficiency and exhibits excellent PSD, but the manufacturing process is slow and expensive and its light output in response to neutrons is anisotropic. Small-molecule organic glass bars offer an easy-to-implement and cost-effective solution to these problems. These properties were characterized to evaluate the efficacy of constructing a compact, low-voltage neutron and gamma-ray imaging system using organic glass bars coupled to silicon photomultiplier arrays. A complete facility for melt-casting organic glass scintillators was setup at the University of Michigan. 6×6×50 mm3 glass bars were produced and the properties listed above were characterized. The first neutron image using organic glass was produced in simple backprojection.

The light output, time resolution, pulse shape discrimination (PSD), neutron light output, and interaction position reconstruction of melt-cast small-molecule organic glass bar scintillators were measured. The trans-stilbene organic scintillator detects fast neutrons and gamma rays with high efficiency and exhibits excellent PSD, but the manufacturing process is slow and expensive and its light output in response to neutrons is anisotropic. Small-molecule organic glass bars offer an easy-to-implement and cost-effective solution to these problems. These properties were characterized to evaluate the efficacy of constructing a compact, low-voltage neutron and gamma-ray imaging system using organic glass bars coupled to silicon photomultiplier arrays. A complete facility for melt-casting organic glass scintillators was setup at the University of Michigan. 6×6×50 mm3 glass bars were produced and the properties listed above were characterized. The first neutron image using organic glass was produced in simple backprojection.

The multi-institution Single-Volume Scatter Camera (SVSC) collaboration led by Sandia National Laboratories (SNL) is developing a compact, high-efficiency double-scatter neutron imaging system. Kinematic emission imaging of fission-energy neutrons can be used to detect, locate, and spatially characterize special nuclear material. Neutron-scatter cameras, analogous to Compton imagers for gamma ray detection, have a wide field of view, good event-by-event angular resolution, and spectral sensitivity. Existing systems, however, suffer from large size and/or poor efficiency. We are developing high-efficiency scatter cameras with small form factors by detecting both neutron scatters in a compact active volume. This effort requires development and characterization of individual system components, namely fast organic scintillators, photodetectors, electronics, and reconstruction algorithms. In this presentation, we will focus on characterization measurements of several SVSC candidate scintillators. The SVSC collaboration is investigating two system concepts: the monolithic design in which isotropically emitted photons are detected on the sides of the volume, and the optically segmented design in which scintillation light is channeled along scintillator bars to segmented photodetector readout. For each of these approaches, we will describe the construction and performance of prototype systems. We will conclude by summarizing lessons learned, comparing and contrasting the two system designs, and outlining plans for the next iteration of prototype design and construction.

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The scintillation anisotropy effect for proton recoil events has been investigated in five pure organic crystalline materials: Anthracene, trans-stilbene, p-terphenyl, bibenzyl, and diphenylacetylene (DPAC). These measurements include the characterization of the scintillation response for one hemisphere of proton recoil directions in each crystal. In addition to standard measurements of the total light output and pulse shape at each angle, the prompt and delayed light anisotropies are analyzed, allowing for the investigation of the singlet and triplet molecular excitation behaviors independently. This paper provides new quantitative and qualitative observations that make progress toward understanding the physical mechanisms behind the scintillation anisotropy. These measurements show that the relationship between the prompt and delayed light anisotropies is correlated with a crystal structure, as it changes between the pi-stacked crystal structure materials (anthracene and p-terphenyl) and the herringbone crystal structure materials (stilbene, bibenzyl, and DPAC). The observations are consistent with a model in which there are preferred directions of kinetic processes for the molecular excitations. These processes and the impact of their directional dependences on the scintillation anisotropy are discussed.

A series of fluorescent silyl-fluorene molecules were synthesized and studied with respect to their photophysical properties and response toward ionizing neutron and gamma-ray radiation. Optically transparent and stable organic glasses were prepared from these materials using a bulk melt-casting procedure. The prepared organic glass monoliths provided fluorescence quantum yields and radiation detection properties exceeding the highest-performing benchmark materials such as solution-grown trans-stilbene crystals. Co-melts based on blends of two different glass-forming compounds were prepared with the goal of enhancing the stability of the amorphous state. Accelerated aging experiments on co-melt mixtures ranging from 0% to 100% of each component indicated improved resistance to recrystallization in the glass blends, able to remain fully amorphous for >1 month at 60 °C. Secondary dopants comprising singlet fluorophores or iridium organometallic compounds provided further improved detection efficiency, as evaluated by light yield and neutron/gamma particle discrimination measurements. Optimized singlet and triplet doping levels were determined to be 0.05 wt % 1,4-bis(2-methylstyryl)benzene singlet fluorophore and 0.28 wt % Ir3+, respectively.

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Here we are investigating the inclusion of organotin compounds in polystyrene material to improve plastic scintillators full gamma-ray energy sensitivity with the ultimate goal of achieving spectroscopy. Accurate evaluation of the relative light yield from the newly developed scintillators is crucial to assess merits of compounds and chemical processes used in the scintillators development and assess the scintillation efficiencies of the newly produced scintillators. Full gamma-ray energy peak in the measured gamma-ray spectrum, resulting from total absorption of gamma-ray energy, would be ideal in assessing the relative light yield. However, the significant number of new samples we are producing for investigation lead us to the possibility of using the Compton edge as an alternate spectral feature that can be exploited for expeditious characterization of the relative light yield in plastic scintillators. In this study we present a spectra gain matching approach, using a spectrum rebinning, for accurate relative light yield measurement using the Compton edge.

In this work we report a new class of organic-based scintillators that combines several of the desirable attributes of existing crystalline, liquid, and plastic organic scintillators. The prepared materials may be isolated in single crystalline form or melt-cast to produce highly transparent glasses that have been shown to provide high light yields of up to 16,000 photons/MeVee, as evaluated against EJ-200 plastic scintillators and solution-grown trans-stilbene crystals. The prepared organic glasses exhibit neutron/gamma pulse-shape discrimination (PSD) and are compatible with wavelength shifters to reduce optical self-absorption effects that are intrinsic to pure materials such as crystalline organics. The combination of high scintillation efficiency, PSD capabilities, and facile scale-up via melt-casting distinguishes this new class of amorphous materials from existing alternatives.