Investigation of CeBr3−xIx scintillators

Matthew Loyd, Luis Stand, Daniel Rutstrom, Yuntao Wu, Jarek Glodo, Kanai Shah, Merry Koschan, Charles L. Melcher, Mariya Zhuravleva

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

CeBr3 is an intrinsic scintillator that has promising performance capabilities such as 60,000 ph/MeV and ~4% energy resolution at 662 keV. It has been shown that halide mixing can improve the light yield of single halide scintillators. In this work we attempted to improve on CeBr3 by creating a mixed halide composition CeBr3−xIx. Analysis of melt-freeze samples revealed that the light yield of CeI3 rapidly increases as bromine is substituted. Thirteen mm diameter crystals were grown using the vertical Bridgman technique, with x values between 0.03 and 1. The CeBr2.5I0.5 crystal segregated into two sections, colorless and green, while the CeBr2I crystal was entirely green. X-ray diffraction analysis was used to identify the two phases. Decay time increased as iodine concentration increased. All colorless phase crystals reached <4.5% energy resolution at 662 keV and >65,000 ph/MeV, with the CeBr2.94I0.06 crystal achieving 3.9% energy resolution at 662 keV. The green phase crystals both reached light yields of 78,000 ph/MeV, the highest ever recorded for a CeI3 phase crystal.

Original languageEnglish
Article number125365
JournalJournal of Crystal Growth
Volume531
DOIs
StatePublished - Feb 1 2020
Externally publishedYes

Funding

This work has been supported by the US Department of Homeland Security, Domestic Nuclear Detection Office , under competitively awarded contract #2012-DN-077-ARI067-05 . The project or effort depicted was sponsored by the Department of Defense, Defense Threat Reduction under grant HDTRA1-19-P-0006. This support does not constitute an expressed or implied endorsement on the part of the Government. The X-ray diffraction experiments were performed at the Joint Institute for Advanced Materials (JIAM) Diffraction Facility, located at the University of Tennessee, Knoxville. The authors would like to thank the Center for Materials Processing at the University of Tennessee for additional support. This work has been supported by the US Department of Homeland Security, Domestic Nuclear Detection Office, under competitively awarded contract #2012-DN-077-ARI067-05. The project or effort depicted was sponsored by the Department of Defense, Defense Threat Reduction under grant HDTRA1-19-P-0006. This support does not constitute an expressed or implied endorsement on the part of the Government. The X-ray diffraction experiments were performed at the Joint Institute for Advanced Materials (JIAM) Diffraction Facility, located at the University of Tennessee, Knoxville. The authors would like to thank the Center for Materials Processing at the University of Tennessee for additional support.

FundersFunder number
Defense Threat ReductionHDTRA1-19-P-0006
U.S. Department of Defense
U.S. Department of Homeland Security
University of Tennessee
Domestic Nuclear Detection Office2012-DN-077-ARI067-05

    Keywords

    • A1. X-ray diffraction
    • B1. Halides
    • B2 Scintillator materials
    • B2. Bridgman technique

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