journal article·2013-10

Synthesis, crystal structure, luminescent properties and photo degradation of mer-tris(8-Hydroxy-quinolinato-N, O)-indium(iii) hydrate 0.5 methanol solvate

Mart-Mari Duvenhage, Hendrik C. Swart, Odireleng M. Ntwaeaborwa, Hendrik G. Visser

Optical Materials· Volume 35· Issue 12
Publisher page

Abstract

Abstract Tris-(8-hydroxyquinioline) aluminium (Alq3) is widely used in organic light emitting diodes as an emission and electron transport layer. In this study the effect of solvent molecules, in the solid state crystal lattice, on the photoluminescence properties of synthesized mer-tris(8-Hydroxy-quinolinato-N, O)-indium(iii) hydrate 0.5 methanol solvate (mer-[In(qn)3]⋅H2O⋅0.5 CH3OH) was studied. Single crystals were obtained through a recrystallization process and single crystal X-ray diffraction was performed to obtain the unit cell structure. The main absorption peaks were assigned to ligand centered electronic transitions, while the solid state photoluminescence excitation peak at 440 nm was assigned to the 0–0 vibronic state of In(qn)3. Broad emission at 510 nm was observed and was ascribed to the relaxation of an excited electron from the S1–S0 level. A powder sample was annealed at 130 °C for 2 h. A decrease in intensity was observed and could possibly be assigned to a loss of solvent species. To study the photon degradation, the sample was irradiated with an UV lamp for ∼15 h. The emission data was collected and the change in photoluminescence intensity with time was monitored. High resolution X-ray photoelectron spectroscopy (XPS) scans of the O-1s peak revealed that after annealing the binding energy shifted to lower energies indicating a possible loss of the H2O and CH3OH present in the crystal. The O-1s peak of the degraded sample indicated the possible formation of C O (∼532.5 eV), C O H and O C O H (∼530.5 eV) on the phenoxide ring.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Metal complexes synthesis and properties · Lanthanide and Transition Metal Complexes

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

References (34)

Show source-provided references
1. Tang · Appl. Phys. Lett. · 1987 · 51 · 91310.1063/1.98799 ↗
2. Tang · Appl. Phys. Lett. · 1989 · 65 · 3610
3. Burrows · Appl. Phys. Lett. · 1994 · 64 · 271810.1063/1.111453 ↗
4. Tai · J. Lumin. · 2011 · 131 · 16910.1016/j.jlumin.2010.09.030 ↗
5. Roselli · Organic Electronics · 2009 · 10 · 141710.1016/j.orgel.2009.08.026 ↗
6. Nunez-Zarur · J. Mol. Struct. · 2008 · 850 · 12710.1016/j.theochem.2007.10.036 ↗
7. Tsuboi · J. Non-Cryst. Solids · 2010 · 356 · 206610.1016/j.jnoncrysol.2010.05.033 ↗
8. Sapochak · J. Am. Chem. Soc. · 2001 · 123 · 630010.1021/ja010120m ↗
9. Liao · J. Am. Chem. Soc. · 2009 · 131 · 76310.1021/ja807284e ↗
10. Chen · Coord. Chem. Rev. · 1998 · 171 · 16110.1016/S0010-8545(98)90027-3 ↗
11. Spaochak · Chem. Mater. · 2004 · 16 · 40110.1021/cm034709r ↗
12. Bankovskii · Zh. Neorg. Khim. Russ. Russ. J. Inorg. Chem. · 1993 · 38 · 1988
13. Korber · J. Chem. Cryst. · 1994 · 24 · 68510.1007/BF01668231 ↗
14. Green · J. Nucl. Med. · 1988 · 29 · 417
15. Nakamoto · Inorg. Chem. · 1971 · 10 · 79810.1021/ic50098a027 ↗
16. SAINT-Plus, version 6.02 (including XPREP); Bruker AXA, Inc.: Madison, WI, USA, 1999.
17. SADABS, version 2004/1; Bruker AXS, Inc.: Madison, WI, USA, 2004.
18. Altomare · J. Appl. Cryst. · 1999 · 32 · 11510.1107/S0021889898007717 ↗
19. Sheldrick · Acta Cryst. · 2008 · A64 · 11210.1107/S0108767307043930 ↗
20. Farrugia · J. Appl. Crystallogr. · 1999 · 32 · 83710.1107/S0021889899006020 ↗
21. Spek · J. Appl. Cryst. · 2003 · 36 · 710.1107/S0021889802022112 ↗
22. K. Brandenburg, H. Putz, DIAMOND, release 3.1b, Crystal Impact GbR: Bonn, Germany, 2005.
23. Rajeswaran · Acta Cryst., Sect. E · 2003 · 59 · m30610.1107/S1600536803009231 ↗
24. Ravi Kishore · Synth. Met. · 2002 · 126 · 19910.1016/S0379-6779(01)00553-7 ↗
25. Stampor · Chem. Phys. Lett. · 1998 · 283 · 37310.1016/S0009-2614(97)01343-2 ↗
26. Walser · Synth. Met. · 1999 · 102 · 155210.1016/S0379-6779(98)00558-X ↗
27. Brinkmann · J. Am. Chem. Soc. · 2000 · 122 · 514710.1021/ja993608k ↗
28. Kumar · Thin Solid Films · 2005 · 477 · 24010.1016/j.tsf.2004.08.144 ↗
29. Rosseli · Org. Electron. · 2009 · 10 · 141710.1016/j.orgel.2009.08.026 ↗
30. Papadimitrakopoulos · Chem. Mater. · 1996 · 8 · 136310.1021/cm960152m ↗
31. Burrows · J. Appl. Phys. · 1996 · 79 · 799110.1063/1.362350 ↗
32. Duvenhage · Phys. B-Condens. Matter · 2012 · 407 · 152110.1016/j.physb.2011.09.076 ↗
33. K. Kontis, in: 28th International Symposium on Shock Waves, vol. 1, Springer-Verlag, Berlin Heidelberg, 2012, pp. 188.10.1007/978-3-642-25685-1 ↗
34. Golovanov · Sens. Actuators B · 2005 · 106 · 56310.1016/j.snb.2004.07.026 ↗