Highly Luminescent NIR-to-Visible Upconversion Thin Films and Monoliths Requiring No High-Temperature Treatment
Source abstract
Abstract
A method is described for producing highly luminescent composite NIR-to-visible upconversion thin films, made from β-NaYF 4:3%Er,17%Yb nanocrystals in a polymethyl methacrylate (PMMA) matrix, which require no postdeposition heat treatment. Nanocrystals are synthesized via a single-phase, high-boiling-point solvent method, which requires neither metal-trifluoroacetate precursors nor the use of autoclaves. Highly luminescent films are produced that can be varied in thickness down to dimensions approaching those of the nanocrystals themselves. The physical properties of the films are characterized by AFM and TEM, whereas the spectroscopic properties are characterized by NIR-to-visible confocal microscopy and by the time-dependence of upconversion luminescence following pulsed NIR excitation. It is shown that dispersal of β-NaYF 4:3%Er,17%Yb nanocrystals in PMMA has no adverse effect on the intrinsic quantum efficiency of upconversion. By focusing the NIR pump beam (980 nm, cw) in the film, linear intensity response and constant color balance are achieved at pump powers down to 40 μW. It is also demonstrated that the thin-film method can be modified to produce large NIR-to-visible upconversion monoliths of high optical quality. This study supports an earlier assertion that the upconversion properties of β-NaYF 4:Er,Yb nanocrystals approach those of the bulk material when nanocrystal size is greater than ∼70 nm.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Luminescence Properties of Advanced Materials · Luminescence and Fluorescent Materials · Radiation Detection and Scintillator Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, University of South Dakota, 414 East Clark Street, Vermillion, South Dakota 57069
References (39)
Show source-provided references
1. Suyver J. F. · Opt. Mater. · 2005 · 27 · 111110.1016/j.optmat.2004.10.021 ↗
2. Chen Z. · J. Am. Chem. Soc. · 2008 · 130 · 302310.1021/ja076151k ↗
3. Lim S. F. · Nano Lett. · 2006 · 6 · 16910.1021/nl0519175 ↗
4. Salthouse C. · Opt. Express · 2008 · 16 · 2173110.1364/OE.16.021731 ↗
5. Zhang P. · J. Am. Chem. Soc. · 2006 · 128 · 1241010.1021/ja0644024 ↗
6. Zhang P. · J. Am. Chem. Soc. · 2007 · 129 · 452610.1021/ja0700707 ↗
7. Hinklin T. R. · Adv. Mater. · 2008 · 20 · 127010.1002/adma.200701235 ↗
8. Downing E. · Science · 1996 · 273 · 118510.1126/science.273.5279.1185 ↗
9. Liu X. · Appl. Opt. · 2008 · 47 · 641610.1364/AO.47.006416 ↗
10. Ho H. P. · Opt. Eng. · 2003 · 42 · 234910.1117/1.1588298 ↗
11. Wang Q. H. · Electron. Lett. · 2004 · 40 · 98710.1049/el:20045046 ↗
12. Shalav A. · Appl. Phys. Lett. · 2005 · 86 · 01350510.1063/1.1844592 ↗
13. Richards B. S. · Synth. Met. · 2005 · 154 · 6110.1016/j.synthmet.2005.07.021 ↗
14. Que W. · Appl. Phys. A: Mater. Sci. Process. · 2001 · 73 · 20910.1007/s003390000623 ↗
15. Sivakumar S. · J. Am. Chem. Soc. · 2005 · 127 · 1246410.1021/ja052583o ↗
16. Sivakumar S. · J. Am. Chem. Soc. · 2007 · 129 · 62010.1021/ja065378x ↗
17. Qin G. · J. Appl. Phys. · 2003 · 93 · 432810.1063/1.1557775 ↗
18. Bubb D. M. · Appl. Phys. Lett. · 2005 · 87 · 13190910.1063/1.2067712 ↗
19. Suyver J. F. · J. Lumin. · 2005 · 114 · 5310.1016/j.jlumin.2004.11.012 ↗
20. Liang X. · Adv. Funct. Mater. · 2007 · 17 · 275710.1002/adfm.200600807 ↗
21. Sun Y. · Nanotechnology · 2007 · 18 · 27560910.1088/0957-4484/18/27/275609 ↗
22. Ghosh P. · J. Phys. Chem. C · 2008 · 112 · 322310.1021/jp7099114 ↗
23. Yi G. S. · Chem. Mater. · 2007 · 19 · 34110.1021/cm062447y ↗
24. Mai H. X. · J. Phys. Chem. C · 2007 · 111 · 1372110.1021/jp073920d ↗
25. Mai H. X. · J. Am. Chem. Soc. · 2006 · 128 · 642610.1021/ja060212h ↗
26. Wang L. · Nano Lett. · 2006 · 6 · 164510.1021/nl060684u ↗
27. Wang L. · Chem. Mater. · 2007 · 19 · 72710.1021/cm061887m ↗
28. Wei Y. · Chem. Mater. · 2006 · 18 · 573310.1021/cm0606171 ↗
29. Yi G. S. · Adv. Funct. Mater · 2006 · 16 · 232410.1002/adfm.200600053 ↗
30. Li C. · Inorg. Chem. · 2007 · 46 · 632910.1021/ic070335i ↗
31. Boyer J. C. · J. Am. Chem. Soc. · 2006 · 128 · 744410.1021/ja061848b ↗
32. Krämer K. W. · Chem. Mater. · 2004 · 16 · 124410.1021/cm031124o ↗
33. Auzel F. · Chem. Rev. · 2004 · 104 · 13910.1021/cr020357g ↗
34. Heer S. · Adv. Mater. · 2004 · 16 · 210210.1002/adma.200400772 ↗
35. Suyver J. F. · J. Lumin. · 2006 · 117 · 110.1016/j.jlumin.2005.03.011 ↗
36. Suyver J. F. · Phys. Rev. B · 2005 · 71 · 12512310.1103/PhysRevB.71.125123 ↗
37. Gamelin D. R. · Top. Curr. Chem. · 2001 · 214 · 110.1007/3-540-44474-2_1 ↗
38. Althues H. · Chem. Soc. Rev. · 2007 · 36 · 145410.1039/b608177k ↗
39. Wang F. · J. Am. Chem. Soc. · 2008 · 130 · 564210.1021/ja800868a ↗