journal article·2017-07

Wavelength‐Tunability and Multiband Emission from Single‐Site Mn2+ Doped CaO Through Antiferromagnetic Coupling and Tailored Superexchange Reactions

Enhai Song, Jinliang Wang, Shi Ye, Xiao‐Bao Yang, Mingying Peng, Qinyuan Zhang, Lothar Wondraczek

Advanced Optical Materials· Volume 5· Issue 13
Publisher page

Abstract

In modern phosphor materials, in contrast to single‐band emission, simultaneous photoluminescence through two or more emission bands enables broad and tailorable emission color, but requires fine control of activator precipitation on specific crystallographic sites. This presents a major obstacle in the design of tunable emitters, since dedicated control of site occupancy is rarely possible. Here, a new paradigm of tunability is considered, which overcomes this limitation. It is demonstrated in CaO:Mn2+ that single‐ and dual‐band emission can be generated by involving only a single type of crystallographic sites. This enables tailoring of the emission color alone through dopant concentration. The two emission bands exhibit different spectral, dynamic, and thermal characteristics, but very similar excitation spectra. While the variations in thermal quenching provide a tool for tunability, the variations in decay behavior suggest interesting potential for lifetime‐multiplexing and coding. Energy transfer is observed between the two emission bands, using time‐resolved emission spectra. From the analysis of crystal structure, spectral data, electron paramagnetic resonance analyses, and density functional theory calculations analyses, it is found that the emission bands at ≈600 and 660 nm originate from isolated Mn2+ ions and superexchange reactions in Mn2+ Mn2+ dimers, respectively.
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Research context

OpenAlex topics: Luminescence Properties of Advanced Materials · Luminescence and Fluorescent Materials · Advanced Photocatalysis Techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

State Key Laboratory of Luminescent Materials and Devices and Institute of Optical Communication Materials South China University of Technology Guangzhou 510641 China

Department of Physics South China University of Technology Guangzhou 510641 China

Otto Schott Institute of Materials Research University of Jena 07743 Jena Germany

Center for Energy and Environmental Chemistry University of Jena 07743 Jena Germany

Funding

National Natural Science Foundation of China · China Postdoctoral Science Foundation

References (53)

Show source-provided references
1. 10.1002/adfm.20100111410.1002/adfm.201001114 ↗
2. 10.1002/adma.20150338010.1002/adma.201503380 ↗
3. 10.1002/adma.20120369210.1002/adma.201203692 ↗
4. 10.1038/am.2016.15610.1038/am.2016.156 ↗
5. 10.1038/ncomms304710.1038/ncomms3047 ↗
6. 10.1002/advs.20150021810.1002/advs.201500218 ↗
7. 10.1021/ja501288x10.1021/ja501288x ↗
8. 10.1016/j.mser.2010.07.00110.1016/j.mser.2010.07.001 ↗
9. 10.1002/adfm.20080101610.1002/adfm.200801016 ↗
10. 10.1038/nmat356510.1038/nmat3565 ↗
11. 10.1143/JPSJ.9.76610.1143/JPSJ.9.766 ↗
12. 10.1016/S0022-2313(02)00541-010.1016/S0022-2313(02)00541-0 ↗
13. 10.1002/adom.20150073210.1002/adom.201500732 ↗
14. 10.1021/jp101772z10.1021/jp101772z ↗
15. 10.1063/1.490174910.1063/1.4901749 ↗
16. Gao G. J. · Phys. Chem. Glasses: Eur. J. Glass Sci. Technol., Part B · 2011 · 52 · 59
17. 10.1063/1.218202610.1063/1.2182026 ↗
18. 10.1149/1.360647410.1149/1.3606474 ↗
19. 10.1039/c1cc14324g10.1039/c1cc14324g ↗
20. 10.1039/C5TC03116H10.1039/C5TC03116H ↗
21. 10.1364/OE.20.02165610.1364/OE.20.021656 ↗
22. 10.1002/adom.20140006610.1002/adom.201400066 ↗
23. 10.1002/advs.20150008910.1002/advs.201500089 ↗
24. 10.1038/nmat401210.1038/nmat4012 ↗
25. 10.1038/ncomms531210.1038/ncomms5312 ↗
26. 10.1039/C4TC01681E10.1039/C4TC01681E ↗
27. 10.1107/S056773947600155110.1107/S0567739476001551 ↗
28. 10.1039/C5DT04341G10.1039/C5DT04341G ↗
29. 10.1016/j.jlumin.2016.05.01410.1016/j.jlumin.2016.05.014 ↗
30. 10.1016/j.jlumin.2008.07.01510.1016/j.jlumin.2008.07.015 ↗
31. 10.1364/OE.18.00254910.1364/OE.18.002549 ↗
32. 10.1039/C6TC02773C10.1039/C6TC02773C ↗
33. 10.1364/OME.3.00018410.1364/OME.3.000184 ↗
34. 10.1149/1.137516910.1149/1.1375169 ↗
35. 10.1016/S0022-2313(96)00103-210.1016/S0022-2313(96)00103-2 ↗
36. 10.1021/cm050638f10.1021/cm050638f ↗
37. 10.1039/C4TC01447B10.1039/C4TC01447B ↗
38. 10.1007/s11664-016-4370-310.1007/s11664-016-4370-3 ↗
39. 10.1007/s10853-011-5317-y10.1007/s10853-011-5317-y ↗
40. 10.1063/1.133279510.1063/1.1332795 ↗
41. 10.1088/0022-3719/5/3/01410.1088/0022-3719/5/3/014 ↗
42. 10.1002/chem.20040028210.1002/chem.200400282 ↗
43. 10.1103/PhysRevB.67.18442010.1103/PhysRevB.67.184420 ↗
44. 10.4294/jpe1952.27.6310.4294/jpe1952.27.63 ↗
45. 10.1016/j.mseb.2013.07.00910.1016/j.mseb.2013.07.009 ↗
46. 10.1016/j.optcom.2013.08.08610.1016/j.optcom.2013.08.086 ↗
47. 10.1021/acs.jpcc.5b0390910.1021/acs.jpcc.5b03909 ↗
48. 10.1039/c4tc00014e10.1039/c4tc00014e ↗
49. 10.1039/C5CS00582E10.1039/C5CS00582E ↗
50. 10.1103/PhysRevB.59.175810.1103/PhysRevB.59.1758 ↗
51. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
52. 10.1039/C5TC03001C10.1039/C5TC03001C ↗
53. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗