KCa4(BO3)3:Ln3+ (Ln = Dy, Eu, Tb) phosphors for near UV excited white–light–emitting diodes
Source abstract
Abstract
A series of doped KCa4(BO3)3:Ln3+ (Ln: Dy, Eu and Tb) compositions were synthesized by solid–state reaction method and their photoluminescent properties were systematically investigated to ascertain their suitability for application in white light emitting diodes. The X–ray diffraction (XRD) and nuclear magnetic resonance (MAS–NMR) data indicates that Ln3+–ions are successfully occupied the non–centrosymmetric Ca2+ sites, in the orthorhombic crystalline phase of KCa4(BO3)3 having space group Ama2, without affecting the boron chemical environment. The present phosphor systems could be efficiently excitable at the broad UV wavelength region, from 250 to 350 nm, compatible to the most commonly available UV light–emitting diode (LED) chips. Photoluminescence studies revealed optimal near white–light emission for KCa4(BO3)3 with 5 wt.% Dy3+ doping, while warm white–light (CIE; X = 0.353, Y = 0.369) is obtained at 1wt.% Dy3+ ion concentration. The principle of energy transfer between Eu3+ and Tb3+ also demonstrates the potential white–light from KCa4(BO3)3:Eu3+,Tb3+ phosphor. Whereas, single Tb3+ and Eu3+–doped systems showed bright green (Tb3+) and red (Eu3+) emissions, respectively. Having structural flexibility along with remarkable chemical/thermal stability and suitable quantum efficiency these phosphors can be promising candidates as white–light–emitter for near UV LEDs.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Luminescence Properties of Advanced Materials · Glass properties and applications · Crystal Structures and Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
University of Aveiro 1 Department of Materials and Ceramics Engineering, , CICECO, 3810–193 Aveiro, Portugal
Indian Institute of Technology Delhi 2 Nanophotonics Laboratory, Department of Physics, , New Delhi, 110016, India
National Taiwan University 3 Department of Chemical Engineering, , Taipei, Taiwan, R.O.C
MIDC 4 Sterlite Technologies Ltd., E–1, E–2, E–3, , Waluj, Aurangabad 431136, Maharashtra, India
University of Aveiro 5 Department of Chemistry, , CICECO, 3810–193 Aveiro, Portugal
References (47)
Show source-provided references
1. Nat. Photonics · 2009 · 3 · 18010.1038/nphoton.2009.32 ↗
2. Science · 2005 · 308 · 127410.1126/science.1108712 ↗
3. Nat. Mater. · 2007 · 6 · 56810.1038/nmat1955 ↗
4. J. Mater. Chem. · 2011 · 21 · 1333410.1039/c1jm11650a ↗
5. J. Mater. Chem. · 2011 · 21 · 686910.1039/c1jm10765h ↗
6. J. Mater. Chem. · 2012 · 22 · 1683910.1039/c2jm32741d ↗
7. Chem. Mater. · 2008 · 20 · 121510.1021/cm7028867 ↗
8. RSC Advances · 2012 · 2 · 876810.1039/c2ra20866k ↗
9. Chem. Mater. · 2005 · 17 · 324210.1021/cm050175d ↗
10. J. Am. Chem. Soc. · 2009 · 131 · 1357210.1021/ja903947b ↗
11. J. Mater. Sci. · 2011 · 46 · 777010.1007/s10853-011-5756-5 ↗
12. Chem. Mater. · 2002 · 14 · 300510.1021/cm011744u ↗
13. Chem. Mater. · 2002 · 14 · 504510.1021/cm020592f ↗
14. J. Electrochem. Soc. · 1998 · 145 · 390310.1149/1.1838891 ↗
15. J. Electrochem. Soc. · 2007 · 154 · J23410.1149/1.2741172 ↗
16. J. Electrochem. Soc. · 2007 · 154 · J3510.1149/1.2388856 ↗
17. Chem. Mater. · 2006 · 18 · 331410.1021/cm060898c ↗
18. Chem. Mater. · 2008 · 20 · 627710.1021/cm801732d ↗
19. Adv. Mater. · 2011 · 23 · 230010.1002/adma.201003640 ↗
20. J. Am. Chem. Soc. · 2009 · 131 · 1357210.1021/ja903947b ↗
21. Chem. Mater. · 2009 · 21 · 31610.1021/cm802394w ↗
22. Chem. Mater. · 2009 · 21 · 128810.1021/cm803233d ↗
23. Chem. Mater. · 2005 · 17 · 324210.1021/cm050175d ↗
24. Appl. Phys. Lett. · 2004 · 84 · 540410.1063/1.1767596 ↗
25. Chem. Mater. · 2005 · 17 · 30810.1021/cm048396r ↗
26. J. Electrochem. Soc. · 2008 · 155 · J6610.1149/1.2825303 ↗
27. J. Lumin. · 2005 · 111 · 13910.1016/j.jlumin.2004.07.005 ↗
28. Electrochem. Solid State Lett. · 2008 · 11 · H335H10.1149/1.2992707 ↗
29. J. Electrochem. Soc. · 2005 · 152 · G88010.1149/1.2060665 ↗
30. Mater. Res. Bull. · 1990 · 25 · 34310.1016/0025-5408(90)90106-C ↗
31. Mater. Sci. Eng., B · 2007 · 139 · 23210.1016/j.mseb.2007.03.001 ↗
32. J. Alloys Compd. · 2004 · 384 · 8810.1016/j.jallcom.2004.04.081 ↗
33. J. Lumin. · 2011 · 131 · 19410.1016/j.jlumin.2010.09.035 ↗
34. Curr. Appl. Phys. · 2011 · 11 · 44210.1016/j.cap.2010.08.017 ↗
35. RSC Advances · 2012 · 2 · 211910.1039/c2ra00808d ↗
36. Inorg. Chem. · 2006 · 45 · 304210.1021/ic051494+ ↗
37. J. Alloys Compd. · 2011 · 509 · 312810.1016/j.jallcom.2010.12.018 ↗
38. J. Alloys Compd. · 1993 · 192
39. Solid State Nucl. Magn. Reson. · 2007 · 31 · 110.1016/j.ssnmr.2006.09.002 ↗
40. Magn. Reson. Chem. · 2002 · 40 · 7010.1002/mrc.984 ↗
41. J. Lumin. · 1997 · 71 · 110.1016/S0022-2313(96)00123-8 ↗
42. J. SolidState Chem. · 1986 · 62 · 20710.1016/0022-4596(86)90233-1 ↗
43. J. Chem. Phys. · 1968 · 49 · 442410.1063/1.1669893 ↗
44. Appl. Phys. Lett. · 2005 · 86 · 21190510.1063/1.1935027 ↗
45. J. Cryst. Growth · 2003 · 256 · 30510.1016/S0022-0248(03)01365-4 ↗
46. J. Appl. Phys. · 2010 · 108 · 04352010.1063/1.3475511 ↗
47. J. Appl. Phys. · 2010 · 107 · 03430110.1063/1.3294964 ↗