Roles of doping ions in persistent luminescence of SrAl2O4:Eu2+, RE3+ phosphors
Source abstract
Abstract
The polycrystalline Eu2+ and RE3+ co-doped strontium aluminates SrAl2O4:Eu2+, RE3+ were prepared by solid state reactions. The UV-excited photoluminescence, persistent luminescence and thermo-luminescence of the SrAl2O4:Eu2+, RE3+ phosphors with different composition and doping ions were studied and compared. The results showed that the doped Eu2+ ion in SrAl2O4:Eu2+, Dy3+ phosphors works as not only the UV-excited luminescent center but also the persistent luminescent center. The doped Dy3+ ion can hardly yield any luminescence under UV-excitation, but can form a electron trap with appropriate depth and greatly enhance the persistent luminescence and thermo-luminescence of SrAl2O4:Eu2+. Different co-doping RE3+ ions showed different effects on persistent luminescence. Only the RE3+ ion (e.g. Dy3+, Nd3+), which has a suitable optical electro-negativity, can form the appropriate electron trap and greatly improve the persistent luminescence of SrAl2O4:Eu2+. Based on above observations, a persistent luminescence mechanism, electron transfer model, was proposed and illustrated.
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Research context
OpenAlex topics: Luminescence Properties of Advanced Materials · Radiation Detection and Scintillator Technologies · Luminescence and Fluorescent Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (19)
Show source-provided references
1. Peng T, Liu H, Yang H, Yan C (2004) Mater Chem Phys 85:6810.1016/j.matchemphys.2003.12.001 ↗
2. Yuan Z-X, Chang C-K, Mao D-L, Ying WJ (2004) J Alloys Compd 377:26810.1016/j.jallcom.2004.01.063 ↗
3. Yamatoto H, Matsuzawa T (1997) J Luminescence 72–74:287
4. Matusuazawa T, Aoki Y, Takeuchi N et al (1996) J Electrochem Soc 143:267010.1149/1.1837067 ↗
5. Jia W, Yuan H, Lu L, Liu H, Yen WM (1998) J Luminescence 76–77:42410.1016/S0022-2313(97)00230-5 ↗
6. Jia W, Yuan H, Holmstrom S et al (1999) J Luminescence 83–84:469
7. Qiu J, Kawasaki M (1998) J Phys Chem Solids 59:152110.1016/S0022-3697(98)00070-5 ↗
8. Aitasaloa T, Deren P, Hölsä J, Jungner H., Krupa J-C et al (2003) J Solid State Chem 171:11410.1016/S0022-4596(02)00194-9 ↗
9. Hölsä J, Jungner H, Lastusaari M et al (2001) J Alloys Compd 323–324:32610.1016/S0925-8388(01)01084-2 ↗
10. Aitasaloa T, Hölsä J, Jungner H et al (2001) J Luminescence 94–95:5910.1016/S0022-2313(01)00279-4 ↗
11. Aitasalo T, Hölsä J, Jungner H et al (2006) J Phys Chem B 110:458910.1021/jp057185m ↗
12. Lü X, Shu W, Huang K (2004) Chinese J Luminescence 25:673
13. Abbruscato V (1971) J Electrochem Soc: Solid State Sci 118:93010.1149/1.2408226 ↗
14. Lin Y, Tang Z, Zhang Z (2003) J Eur Ceram Soc 23:17510.1016/S0955-2219(02)00080-8 ↗
15. Sakai R, Katsumata T, Komuro S, Morikawa T (1999) J Luminescence 85:14910.1016/S0022-2313(99)00061-7 ↗
16. McKeever SWS (1985) Thermoluminescence of Solid, 1st edn. London, Cambridge University Press, p. 8510.1017/CBO9780511564994 ↗
17. Kim TK, Woo JJ, Choe HS et al (1999) Radiat Prot Dosi 84(3):29710.1093/oxfordjournals.rpd.a032743 ↗
18. Su Q (1993) Rare Earth Chemistry, 1st edn. Science and Technology Press, Zhenzhou, p. 13
19. Nag A, Kutty TRN (2003) J Alloys Compd 354:22110.1016/S0925-8388(03)00009-4 ↗