The gadolinium effect on crystallization behavior and luminescence of β‐NaYF 4 :Yb,Er phase
Source abstract
Abstract
Abstract Single phase β‐NaY 0.8‐ x Gd x Yb 0.18 Er 0.02 F 4 nanoparticles with different concentrations of gadolinium ions were prepared via PVP‐assisted solvothermal treating at 200°C (PVP‐ polyvinylpyrrolidone). With the increase in Gd 3+ concentration, size of the nanoparticles decreased. The up‐converting spectra recorded upon 980 nm irradiation showed the green (510‐560 nm) and red (640‐690 nm) emissions, due to 2 H 11/2 , 4 S 3/2 → 4 I 15/2 and 4 F 9/2 → 4 I 15/2 transitions, respectively. The strongest up‐conversion luminescence was detected in 15 mol% Gd 3+ ‐doped nanoparticles obtained after 20 hours of solvothermal treating. With the rise of Gd 3+ content up‐conversion emission decreased due to increased defect concentration in the NaYF 4 matrix. Fourier transform infrared spectroscopy proved in situ generation of hydrophilic nanoparticles as a result of PVP ligands retention at the particle surface.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Luminescence Properties of Advanced Materials · Inorganic Fluorides and Related Compounds · Perovskite Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Innovation Center of the Faculty of Chemistry University of Belgrade Belgrade Serbia
Institute of Technical Sciences of SASA Belgrade Serbia
Faculty of Mining and Geology University of Belgrade Belgrade Serbia
Photonic Center Institute of Physics Belgrade University of Belgrade Belgrade Serbia
School of Petroleum and Chemical Engineering Dalian University of Technology Dalian China
Funding
Ministry of Education, Science and Technological Development of Serbia project OI
References (38)
Show source-provided references
1. 10.1039/C6CP04413A10.1039/C6CP04413A ↗
2. 10.1016/j.jallcom.2015.04.11210.1016/j.jallcom.2015.04.112 ↗
3. 10.1002/adma.20090172210.1002/adma.200901722 ↗
4. 10.1016/j.materresbull.2018.09.01510.1016/j.materresbull.2018.09.015 ↗
5. 10.1016/j.ceramint.2012.07.03610.1016/j.ceramint.2012.07.036 ↗
6. 10.1039/C7NR08758F10.1039/C7NR08758F ↗
7. 10.1088/0957-4484/18/27/27560910.1088/0957-4484/18/27/275609 ↗
8. 10.1016/S1002-0721(17)60929-310.1016/S1002-0721(17)60929-3 ↗
9. 10.1016/j.biomaterials.2012.08.02910.1016/j.biomaterials.2012.08.029 ↗
10. 10.1111/ijac.1302510.1111/ijac.13025 ↗
11. 10.1016/j.dyepig.2017.11.05010.1016/j.dyepig.2017.11.050 ↗
12. 10.1039/C8RA04178D10.1039/C8RA04178D ↗
13. 10.1016/j.saa.2017.10.06010.1016/j.saa.2017.10.060 ↗
14. 10.1088/1757-899X/73/1/01212010.1088/1757-899X/73/1/012120 ↗
15. 10.1016/j.phpro.2015.10.02910.1016/j.phpro.2015.10.029 ↗
16. 10.1021/jp411950210.1021/jp4119502 ↗
17. 10.1002/adfm.20030504410.1002/adfm.200305044 ↗
18. 10.1016/j.jeurceramsoc.2017.05.00610.1016/j.jeurceramsoc.2017.05.006 ↗
19. 10.1016/j.jeurceramsoc.2015.07.01710.1016/j.jeurceramsoc.2015.07.017 ↗
20. 10.1111/ijac.1276910.1111/ijac.12769 ↗
21. 10.1186/s11671-017-2306-310.1186/s11671-017-2306-3 ↗
22. 10.1111/j.1551-2916.2011.04518.x10.1111/j.1551-2916.2011.04518.x ↗
23. 10.1016/j.apt.2016.09.02110.1016/j.apt.2016.09.021 ↗
24. 10.1016/j.optmat.2017.10.01210.1016/j.optmat.2017.10.012 ↗
25. 10.1002/anie.20150883810.1002/anie.201508838 ↗
26. 10.1016/j.matlet.2008.10.02810.1016/j.matlet.2008.10.028 ↗
27. 10.1021/cm071668g10.1021/cm071668g ↗
28. 10.1016/j.ab.2011.11.00810.1016/j.ab.2011.11.008 ↗
29. 10.1039/C5NR04125B10.1039/C5NR04125B ↗
30. 10.1039/c0cc05722c10.1039/c0cc05722c ↗
31. 10.1016/j.apt.2015.11.01010.1016/j.apt.2015.11.010 ↗
32. 10.1038/nature0877710.1038/nature08777 ↗
33. 10.1016/j.jallcom.2009.05.13810.1016/j.jallcom.2009.05.138 ↗
34. 10.1021/jp06333810.1021/jp063338 ↗
35. 10.1134/S107042721309025410.1134/S1070427213090254 ↗
36. 10.1002/anie.20100395910.1002/anie.201003959 ↗
37. 10.1039/C2NR32482B10.1039/C2NR32482B ↗
38. 10.1039/C6RA20382E10.1039/C6RA20382E ↗