journal article·2012-10-01Open access

Preparation of 8-hydroxyquinoline wires by decomposition of tris(8-hydroxyquinoline) aluminium

Man Kin Fung, Alan Man Ching Ng, Aleksandra B. Djurišić, Wai Kin Chan, Hai Wang

Abstract

We fabricated 8-hydroxyquinoline (HQ) wires by two methods, decomposition of tris(HQ) aluminium at low pressure in a tube furnace and heating of HQ powder at atmospheric pressure. Fabricated wires were crystalline, and exhibited the same optical properties (absorption and photoluminescence) as HQ powder. While the properties of wires prepared by two different methods were the same, it should be noted that synthesis by decomposition of tris(HQ) aluminium required elimination of mechanical vibration of the growth tube. Implications of decomposition of tris(HQ) aluminium during organic vapour phase deposition growth on organic optoelectronic device performance are discussed.
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Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Molecular Junctions and Nanostructures · Organic Electronics and Photovoltaics

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

Affiliations

Department of Physics, The University of Hong Kong , Pokfulam Road, Pokfulam, Hong Kong

Department of Chemistry, The University of Hong Kong , Pokfulam Road, Pokfulam, Hong Kong

References (27)

Show source-provided references
1. 10.1016/S0379-6779(97)80214-710.1016/S0379-6779(97)80214-7 ↗
2. 10.1021/cm960152m10.1021/cm960152m ↗
3. 10.1021/cm970599a10.1021/cm970599a ↗
4. 10.1063/1.243507010.1063/1.2435070 ↗
5. 10.1063/1.348605810.1063/1.3486058 ↗
6. 10.1039/b514898g10.1039/b514898g ↗
7. 10.1016/0040-6031(87)80055-210.1016/0040-6031(87)80055-2 ↗
8. 10.1016/j.saa.2004.06.02910.1016/j.saa.2004.06.029 ↗
9. 10.1007/s10971-008-1810-410.1007/s10971-008-1810-4 ↗
10. 10.1016/j.elecom.2009.12.03510.1016/j.elecom.2009.12.035 ↗
11. 10.1016/j.apsusc.2009.12.12610.1016/j.apsusc.2009.12.126 ↗
12. 10.1016/j.molstruc.2009.07.01510.1016/j.molstruc.2009.07.015 ↗
13. 10.1016/j.saa.2004.05.03010.1016/j.saa.2004.05.030 ↗
14. 10.1016/S0921-5107(03)00067-910.1016/S0921-5107(03)00067-9 ↗
15. 10.1016/j.cplett.2004.07.00110.1016/j.cplett.2004.07.001 ↗
16. 10.1016/j.msea.2007.03.09510.1016/j.msea.2007.03.095 ↗
17. 10.1002/adma.20070280910.1002/adma.200702809 ↗
18. 10.1016/j.tsf.2010.04.01910.1016/j.tsf.2010.04.019 ↗
19. 10.1166/jnn.2009.110510.1166/jnn.2009.1105 ↗
20. 10.1016/j.synthmet.2004.10.00110.1016/j.synthmet.2004.10.001 ↗
21. 10.1002/pssa.20040434110.1002/pssa.200404341 ↗
22. 10.1021/ja993608k10.1021/ja993608k ↗
23. 10.1002/adfm.20080049210.1002/adfm.200800492 ↗
24. 10.1016/j.jphotochem.2006.01.00410.1016/j.jphotochem.2006.01.004 ↗
25. 10.1016/j.clay.2006.08.00310.1016/j.clay.2006.08.003 ↗
26. 10.1107/S056774087800486010.1107/S0567740878004860 ↗
27. 10.1063/1.133241910.1063/1.1332419 ↗