Synthesis of cerium-doped gadolinium gallium aluminum garnet (GGAG:Ce) scintillating powder via solvothermal method

被引:1
|
作者
Oad, Nisha [1 ]
Pandya, Divya [2 ]
Rawat, Sheetal [2 ]
Chandra, Prakash [1 ]
Tyagi, Mohit [3 ]
Tripathi, Brijesh [2 ]
Gurrala, Pavan [4 ]
机构
[1] Pandit Deendayal Energy Univ, Sch Energy Technol, Dept Chem, Gandhinagar 382426, India
[2] Pandit Deendayal Energy Univ, Sch Energy Technol, Dept Phys, Gandhinagar 382426, India
[3] Bhabha Atom Res Ctr, Tech Phys Div, Mumbai 400085, India
[4] Pandit Deendayal Energy Univ, Sch Technol, Dept Mech Engn, Gandhinagar 382426, India
关键词
GGAG; Ce doped; garnet; scintillator; solvothermal; radiation spectroscopy; PERSISTENT LUMINESCENCE; CERAMICS;
D O I
10.1088/1402-4896/ad30e2
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
The powder material Gd3Ga3Al2O12:Ce (GGAG doped with Cerium) has garnered significant attention in radiation detection due to its high light yield and rapid decay time. Despite its potential, the synthesis of high-quality and reproducible GGAG:Ce scintillating powder remains a considerable challenge. In this study, we present a solvothermal approach with an annealing temperature of 1300 degrees C for producing cerium-doped GGAG powder with varying concentrations (4, 2, and 0.5 mol%). The structural and luminescent characteristics were meticulously examined using X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), photoluminescence (PL), radioluminescence (RL) spectroscopy, and X-ray photoelectron spectroscopy (XPS). XRD analysis confirmed the single-cubic phase garnet structure of the synthesized powder. By comparing the intermediate solvothermal products synthesized at different sintering temperatures (900 degrees C for 3 h and 1300 degrees C for 1 and 3 h), a direct correlation between solvothermal conditions and the structure/property relationships of the product was established. FESEM images revealed an ellipsoidal to irregular morphology of the as-synthesized GGAG:Ce microparticles, ranging from 0.1 to 0.3 mu m, regardless of the Ce concentration. PL spectra demonstrated a strong emission peak at approximately 550 nm, characteristic of Ce3+ ions. RL data confirmed the peak luminescence at around 550 nm, with an almost twofold increase in intensity as the concentration of Ce3+ increased from 0.5 mol% to 4 mol%. XPS data disclosed the Ce3+/Ce4+ ratio in solvothermally synthesized GGAG:Ce, wherein Ce loading of 4 mol% demonstrated the increase in Ce3+ concentration to 95%, whereas the concentration of Ce4+ decreased to 5%. Notably, the highest luminescence efficiency was achieved with GGAG:Ce at a 4 mol% concentration. Thus, the solvothermal method employed in GGAG:Ce synthesis presents a straightforward approach, yielding rapid results with precise control over particle morphology and size.
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页数:12
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