Highly Luminescent and Photostable Quantum Dot–Silica Monolith and Its Application to Light-Emitting Diodes
Source abstract
Abstract
A highly luminescent and photostable quantum dot-silica monolith (QD-SM) substance was prepared by preliminary surface exchange of the QDs and base-catalyzed sol-gel condensation of silica. The SM was heavily doped with 6-mercaptohexanol exchanged QDs up to 12 vol % (26 wt %) without particle aggregation. Propylamine catalyst was important in maintaining the original luminescence of the QDs in the SM during sol-gel condensation. The silica layer was a good barrier against oxygen and moisture, so that the QD-SM maintained its initial luminescence after high-power UV radiation (∼1 W) for 200 h and through the 150 °C LED encapsulant curing process. Green and red light-emitting QD-SMs were applied as color-converting layers on blue LEDs, and the external quantum efficiency reached up to 89% for the green QD-SM and 63% for the red one. A white LED made with a mixture of green and red QDs in the SM, in which the color coordinate was adjusted at (0.23, 0.21) in CIE1931 color space for a backlight application, showed an efficacy of 47 lm/W, the highest value yet reported.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Quantum Dots Synthesis And Properties · Carbon and Quantum Dots Applications · Luminescence Properties of Advanced Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Advanced Material Research Center, Samsung Advanced Institute of Technology, Samsung Electronics Co. Mt.14-1, Nongseo-Dong, Giheung-Gu, Yongin-Si, Gyeonggi-Do 449-712, Korea
References (29)
Show source-provided references
1. Hines M. A. · J. Phys. Chem. · 1996 · 100 · 46810.1021/jp9530562 ↗
2. Peng X. · J. Am. Chem. Soc. · 1997 · 119 · 701910.1021/ja970754m ↗
3. Dabbousi B. O. · J. Phys. Chem. B · 1997 · 101 · 946310.1021/jp971091y ↗
4. Steckel J. S. · Angew. Chem., Int. Ed. · 2004 · 43 · 215410.1002/anie.200453728 ↗
5. Jun S. · Chem. Commun. · 2005 · 461610.1039/b509196a ↗
6. Steckel J. S. · Angew. Chem., Int. Ed. · 2006 · 45 · 579610.1002/anie.200600317 ↗
7. Lim J. · Adv. Mater. · 2007 · 19 · 192710.1002/adma.200602642 ↗
8. Haubold S. · ChemPhysChem · 2001 · 2 · 33110.1002/1439-7641(20010518)2:5<331::AID-CPHC331>3.0.CO;2-0 ↗
9. Xie R. · J. Am. Chem. Soc. · 2007 · 129 · 1543210.1021/ja076363h ↗
10. Chen Y. · J. Am. Chem. Soc. · 2008 · 130 · 502610.1021/ja711379k ↗
11. Pal B. N. · Nano Lett. · 2012 · 12 · 33110.1021/nl203620f ↗
12. Jang E. · Adv. Mater. · 2010 · 22 · 307610.1002/adma.201000525 ↗
13. Jun S. · Angew. Chem., Int. Ed. · 2013 · 52 · 67910.1002/anie.201206333 ↗
14. Lee J. · Adv. Mater. · 2000 · 12 · 110210.1002/1521-4095(200008)12:15<1102::AID-ADMA1102>3.0.CO;2-J ↗
15. Stöber W. · J. Colloid Interface Sci. · 1968 · 26 · 6210.1016/0021-9797(68)90272-5 ↗
16. Alejandro-Arellano M. · Pure Appl. Chem. · 2000 · 72 · 25710.1351/pac200072010257 ↗
17. Yang P. · Chem. Commun. · 2010 · 46 · 459510.1039/c002243h ↗
18. Selvan S. T. · Adv. Mater. · 2005 · 17 · 162010.1002/adma.200401960 ↗
19. Selvan S. T. · Angew. Chem., Int. Ed. · 2007 · 46 · 244810.1002/anie.200604245 ↗
20. Li C. · Langmuir · 2004 · 20 · 110.1021/la035546o ↗
21. Yang P. · Langmuir · 2005 · 21 · 891310.1021/la050397q ↗
22. Zhoua X. · Appl. Surf. Sci. · 2005 · 242 · 28110.1016/j.apsusc.2004.08.022 ↗
23. Riassetto D. · Nanosci. Nanotechnol. Lett. · 2011 · 3 · 65510.1166/nnl.2011.1228 ↗
24. Wang Q. · Chem. Mater. · 2005 · 17 · 476210.1021/cm050962a ↗
25. Sorensen L. · Adv. Mater. · 2006 · 18 · 196510.1002/adma.200600791 ↗
26. Chan Y. · J. Am. Chem. Soc. · 2006 · 128 · 314610.1021/ja057980d ↗
27. Arachchige I. U. · J. Am. Chem. Soc. · 2007 · 129 · 184010.1021/ja066749c ↗
28. Selvan S. T. · Adv. Mater. · 2001 · 13 · 98510.1002/1521-4095(200107)13:12/13<985::AID-ADMA985>3.0.CO;2-W ↗
29. Lunz M. · Phys. Rev. B · 2010 · 81 · 20531610.1103/PhysRevB.81.205316 ↗