Tl concentration and its variation in a CsI(Tl) crystal for the CALIFA detector

A. Knyazev, J. Park, P. Golubev, J. Pallon, J. Cederkall, H. Alvarez-Pol, J. Benlliure, J. A. Briz, P. Cabanelas, E. Casarejos, D. Cortina-Gil, P. Díaz Fernández, M. Feijoo, D. Galaviz, E. Galiana, M. J.G. Borge, R. Gernhäuser, D. Gonzalez, C. Gutierrez-Neira, A. L. HartigA. Heinz, B. Heiss, H. Johansson, P. Klenze, T. Kröll, T. Nilsson, A. Perea, L. Ponnath, H. B. Rhee, J. L. Rodriguez-Sanchez, O. Tengblad, P. Teubig

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskriftPeer review

    Sammanfattning

    One of the factors that can contribute to the resolution of long, doped inorganic scintillators used for nuclear spectroscopy is the variation of the dopant concentration over the length the detector crystal. In this work an investigation of such potential variations in one of the CsI(Tl) scintillators used in the calorimeter, CALIFA, of the R3B experiment at FAIR, has been performed using particle induced X-ray emission. No statistically significant gradient in doping level was found along the long axis of the investigated sample crystal and the mean value of the Tl concentration was measured to be 0.0839(38)% by weight. This corresponds to a light output of 97.3−1.7 +1.3% relative to the maximum attainable light output according to previously published work. By taking the ±1σ bounds, the 3% statistical spread in the relative light output provides a good reference value of the minimum light-output non-uniformity observed for the CALIFA crystals. If the relative light output is estimated pointwise from a set of Tl concentration measurements a light-output non-uniformity of 4.6(2.4)% results. For a γ-ray energy of 662 keV the deduced variation in Tl concentration contributes with 0.48(6)% to the typical resolution of 7.74(6)% measured with a collimated source along the crystal main axis. The result is of interest for the characterization of the detector system performance and for realistic simulations of the light collection process in detector systems that are used for nuclear spectroscopy and calorimetry.

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