journal article·2018-11

Preparation and luminescent properties of Eu(Ⅲ) organic complex and novel transparent ethylene-methyl acrylate copolymer (EMA) films doped with complexes

Zihan Gao, Yuewen Wu, Lei Xu, Haixia Hao, Qingyao Wu, Hongde Xie

Optical Materials· Volume 85
Publisher page

Abstract

Abstract In this study, a new ternary rare earth organic complex Eu(POA)3TTA was synthesized and successfully doped into the ethylene-methyl acrylate copolymer (EMA) resins. The transparent doped EMA (Eu-EMA) films with excellent fluorescence performance were obtained by making full use of the excellent compatibility and filling performance of EMA resins. Fourier transform infrared spectrometer (FT-IR), elemental analysis, MALDI-TOF MS, scanning electron microscope (SEM), photoluminescence tests, thermogravimetric analysis (TGA) and static water contact angle measurements were used to characterize the properties of the complexes Eu(POA)3TTA and the Eu-EMA films. FT-IR analysis, elemental analysis and MALDI-TOF MS verify the ligands were successfully coordinated with the Eu3+ ions. The Eu(POA)3TTA particles are well dispersed in the EMA matrix and only a small fraction of them precipitate out to the surface of the EMA films. The relationship between fluorescence emission intensity of the Eu-EMA films and the doping ratios of Eu(POA)3TTA to EMA resins has been studied and discussed. The fluorescence intensity of the Eu-EMA films reaches the maximum when the doping ratio is 1.0 wt%. The Eu-EMA films all have high thermal stability (Td ≥ 392 °C) and the Td value enhances as the doping ratio increasing. As a result, the Eu-EMA films possess potential application for luminescent materials even at high temperatures.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Lanthanide and Transition Metal Complexes · Magnetism in coordination complexes · Radioactive element chemistry and processing

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

References (38)

Show source-provided references
1. Poomalai · Polym. Plast. Technol. Eng. · 2009 · 48 · 95810.1080/03602550902996685 ↗
2. Cavodeau · Polym. Degrad. Stabil. · 2017 · 144 · 40110.1016/j.polymdegradstab.2017.08.016 ↗
3. Ding · J. Polym. Eng. · 2016 · 3610.1515/polyeng-2015-0299 ↗
4. Yang · Synth. Met. · 2016 · 221 · 23610.1016/j.synthmet.2016.08.016 ↗
5. Sengar · Sensor. Actuator. B Chem. · 2017 · 241 · 56710.1016/j.snb.2016.10.119 ↗
6. Liu · Synth. Met. · 2009 · 159 · 155710.1016/j.synthmet.2009.04.013 ↗
7. Li · React. Funct. Polym. · 2009 · 69 · 24010.1016/j.reactfunctpolym.2009.01.008 ↗
8. Lima · Org. Electron. · 2014 · 15 · 79810.1016/j.orgel.2014.01.009 ↗
9. Azab · Spectrochim. Acta Mol. Biomol. Spectrosc. · 2010 · 75 · 2110.1016/j.saa.2009.09.008 ↗
10. Binnemans · Chem. Rev. · 2009 · 109 · 428310.1021/cr8003983 ↗
11. Gavriluta · Adv. Opt. Mater. · 2016 · 4 · 184610.1002/adom.201600395 ↗
12. Liu · Eur. Polym. J. · 2009 · 45 · 226010.1016/j.eurpolymj.2009.05.014 ↗
13. Wu · Opt. Mater. · 2017 · 72 · 43610.1016/j.optmat.2017.06.042 ↗
14. Hao · Opt. Mater. · 2017 · 72 · 810.1016/j.optmat.2017.04.013 ↗
15. Wu · Opt. Mater. · 2018 · 80 · 6510.1016/j.optmat.2018.04.040 ↗
16. Liu · J. Am. Chem. Soc. · 2014 · 136 · 970110.1021/ja5042989 ↗
17. Nouri · Optik - Int. J. Light Electron. Optic. · 2017 · 139 · 10410.1016/j.ijleo.2017.03.075 ↗
18. Kłonkowski · 2000
19. Fermi · Chemistry · 2014 · 20 · 1066110.1002/chem.201402021 ↗
20. D’Aléo · Coord. Chem. Rev. · 2012 · 256 · 160410.1016/j.ccr.2012.03.023 ↗
21. Martins · J. Fluoresc. · 2010 · 20 · 73910.1007/s10895-010-0616-2 ↗
22. Li · Inorg. Chim. Acta. · 2015 · 426 · 10710.1016/j.ica.2014.11.035 ↗
23. Chen · Eur. Polym. J. · 2014 · 58 · 19110.1016/j.eurpolymj.2014.07.003 ↗
24. Liu · Polyhedron · 2016 · 118 · 2510.1016/j.poly.2016.07.034 ↗
25. Gao · Spectrochim. Acta Mol. Biomol. Spectrosc. · 2015 · 150 · 56510.1016/j.saa.2015.05.078 ↗
26. Małecki · Struct. Chem. · 2008 · 19 · 25710.1007/s11224-007-9280-9 ↗
27. Gao · J. Photochem. Photobiol. Chem. · 2016 · 324 · 2310.1016/j.jphotochem.2016.02.013 ↗
28. Shao · Org. Electron. · 2011 · 12 · 64110.1016/j.orgel.2011.01.011 ↗
29. Zhang · J. Rare Earths · 2007 · 25 · 14310.1016/S1002-0721(07)60062-3 ↗
30. Teotonio · J. Lumin. · 2008 · 128 · 19010.1016/j.jlumin.2007.07.005 ↗
31. Lv · J. Alloy. Comp. · 2009 · 468 · 40610.1016/j.jallcom.2008.01.049 ↗
32. Sun · J. Photochem. Photobiol. Chem. · 2011 · 219 · 24310.1016/j.jphotochem.2011.02.026 ↗
33. Huang · J. Rare Earths · 2012 · 30 · 58610.1016/S1002-0721(12)60095-7 ↗
34. Shipeng · J. Rare Earths · 2006 · 24 · 71210.1016/S1002-0721(07)60014-3 ↗
35. Gao · J. Men, Polymer · 2012 · 53 · 470910.1016/j.polymer.2012.07.059 ↗
36. Yan · Opt. Mater. · 2007 · 30 · 61710.1016/j.optmat.2007.01.015 ↗
37. Garcia-Torres · J. Photochem. Photobiol. Chem. · 2014 · 283 · 810.1016/j.jphotochem.2014.03.013 ↗
38. Liao · J. Lumin. · 2010 · 130 · 76210.1016/j.jlumin.2009.11.028 ↗