4.6 Article

Ce3+, Pr3+ Co-Doped Lu3Al5O12 Single Crystals and Ceramics: A Comparative Study

Journal

MATERIALS
Volume 15, Issue 24, Pages -

Publisher

MDPI
DOI: 10.3390/ma15249025

Keywords

Ce; Pr; LuAG; optical floating zone method; scintillator ceramics; garnet; single crystals

Funding

  1. National Natural Science Foundation of China
  2. Strategic Priority Research Program of the Chinese Academy of Sciences [62175249, 61475175, 11005139]
  3. Research Program of Shanghai Sciences and Technology Commission Foundation [XDA22010301]
  4. Russian Ministry of Science and Higher Education [22511100300]
  5. [00657-2020-0006]

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Ce3+, Pr3+ co-doped Lu3Al5O12 (Ce, Pr:LuAG) single crystals and ceramics were prepared using different methods, and their microstructure, luminescence performance, and scintillation light yield were compared. The results showed that the ceramics had a faster scintillation decay and higher scintillation light yield.
Ce3+, Pr3+ co-doped Lu3Al5O12 (Ce, Pr:LuAG) single crystals and ceramics were prepared using the optical floating zone (OFZ) and reactive vacuum sintering methods, respectively. The microstructure, photo- (lambda(ex) = 450 nm), and radio-luminescence (under X-ray excitation) performance, as well as scintillation light yield (LY, under gamma-ray, Cs-137 source) of both materials, were investigated and compared. Ce, Pr:LuAG ceramics had an in-line transmittance of approximately 20% in the visible light range, while the analogous crystals were more transparent (similar to 65%). The X-ray excited luminescent (XEL) spectra showed the characteristic Ce (3+) and Pr3+ emissions located at 310 nm, 380 nm, and 510 nm. The highest LY of the Ce, Pr:LuAG ceramics reached 34,112 pho/MeV at 2 mu s time gate, which is higher than that of a single crystal. The ratio of LY values (LY2/LY0.75) between shaping times of 0.75 mu s and 2 mu s indicated a faster scintillation decay of ceramics regarding single crystals. It was ascribed to the lower effective concentration of luminescent activators in single crystals because of the coefficient segregation effect.

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