Photoionization behavior of Eu2+-doped BaMgSiO4 long-persisting phosphor upon UV irradiation
Source abstract
Abstract
Abstract The fluorescence, phosphorescence and thermoluminescence properties of Eu-doped BaMgSiO4 phosphors sintered in air and in a reducing atmosphere were investigated. Phosphorescence of phosphor sintered in a reducing atmosphere can last for 1.5 h at a recognizable intensity level, whereas phosphorescence of air-sintered phosphor can only persist for 6 min. In addition, a distinction between the shape of the fluorescence spectrum and its corresponding phosphorescence spectrum is observed in the former case. Ionization of Eu2+ to Eu3+ upon UV irradiation is observed in the phosphor prepared in a reducing atmosphere, but there is no indication that the photogenerated Eu3+ cannot change back to its divalent state at room temperature after the excitation source is switched off. In addition, phosphor sintered in a reducing atmosphere shows photochromism upon UV irradiation. No such photoionization and photochromism behavior is observed for the air-sintered phosphor. A possible Eu2+ photoionization mechanism is constructed on the basis of these experimental observations. The photoionization mechanism presented can also successfully explain the fluorescence and phosphorescence behavior of Eu in BaMgSiO4.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Luminescence Properties of Advanced Materials · Solid-state spectroscopy and crystallography · Radiation Detection and Scintillator Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (32)
Show source-provided references
1. Matsuzawa · J Electrochem Soc · 1996 · 143 · 267010.1149/1.1837067 ↗
2. Höpe · J Phys Chem Solids · 2000 · 61 · 200110.1016/S0022-3697(00)00194-3 ↗
3. Kowatari · Nucl Instrum Methods Phys Res, Sect A · 2002 · 480 · 43110.1016/S0168-9002(01)00922-6 ↗
4. Xu · Appl Phys Lett · 1999 · 74 · 241410.1063/1.123865 ↗
5. Jia · J Electrochem Soc · 2003 · 150 · H6110.1149/1.1553792 ↗
6. Boutinaud · J Phys D: Appl Phys · 2009 · 42 · 04510610.1088/0022-3727/42/4/045106 ↗
7. Lei · Opt Mater · 2007 · 29 · 149110.1016/j.optmat.2006.07.011 ↗
8. Murazaki · Jpn Rare Earth · 1999 · 35 · 41
9. Trojan-Piegza · Chem Mater · 2008 · 20 · 225210.1021/cm703060c ↗
10. Liu · Chem Mater · 2005 · 17 · 210810.1021/cm0496422 ↗
11. Clabau · Chem Mater · 2005 · 17 · 390410.1021/cm050763r ↗
12. Aitasalo · J Phys Chem B · 2006 · 110 · 458910.1021/jp057185m ↗
13. Aitasalo · J Solid State Chem · 2003 · 171 · 11410.1016/S0022-4596(02)00194-9 ↗
14. Dorenbos · Phys Status Solidi B · 2005 · 242 · 710.1002/pssb.200590001 ↗
15. Clabau · Chem Mater · 2006 · 18 · 321210.1021/cm052728q ↗
16. Hölsä · J Lumin · 2009 · 129 · 160610.1016/j.jlumin.2008.12.027 ↗
17. Chen · J Lumin · 2006 · 118 · 7010.1016/j.jlumin.2005.05.011 ↗
18. Hassinen · Opt Mater · 2009 · 31 · 175110.1016/j.optmat.2009.01.016 ↗
19. Peng M. MD thesis, 2003.
20. Denis · Inorg Chem · 2008 · 47 · 422610.1021/ic702240q ↗
21. Peng · J Mater Chem · 2003 · 13 · 120210.1039/b211624c ↗
22. Liu · J Solid State Chem · 1993 · 102 · 11510.1006/jssc.1993.1013 ↗
23. Jia · J Appl Phys · 2007 · 101 · 02352010.1063/1.2409767 ↗
24. Sivakumar · J Electrochem Soc · 2007 · 154 · J16710.1149/1.2714303 ↗
25. Qiu · J Mater Res · 2001 · 16 · 8810.1557/JMR.2001.0017 ↗
26. Hölsä · J Alloys Compd · 2001 · 323 · 32610.1016/S0925-8388(01)01084-2 ↗
27. Clabau · J Solid State Chem · 2008 · 181 · 145610.1016/j.jssc.2008.03.011 ↗
28. Bizarri · J Lumin · 2005 · 113 · 19910.1016/j.jlumin.2004.09.119 ↗
29. Oshio · J Electrochem Soc · 1998 · 145 · 390310.1149/1.1838891 ↗
30. Zeng · Appl Phys Lett · 2006 · 88 · 05190610.1063/1.2168492 ↗
31. Nogami · J Lumin · 1998 · 78 · 6310.1016/S0022-2313(97)98281-8 ↗
32. Nogami · Phys Rev B · 1997 · 56 · 18210.1103/PhysRevB.56.182 ↗