Novel electroluminescent devices containing Eu3+-(2-acyl-1,3-indandionate) complexes with TPPO ligand
Source abstract
Abstract
Abstract Fabrication and electroluminescent properties of devices containing europium complexes of general formula [Eu(ACIND) 3 (TPPO) 2 ], where ACIND, 2-acyl-1,3-indandionate ligands; and TPPO, triphenylphosphine oxide, as emitter layers are discussed. The double-layer devices based on these complexes present the following configurations: device 1 : ITO/TPD/[Eu(AIND) 3 (TPPO) 2 ]/Al; device 2 : ITO/TPD/[Eu(ISOVIND) 3 (TPPO) 2 ]/Al and device 3 : ITO/TPD/[Eu(BIND) 3 (TPPO) 2 ]/Al, where AIND, 2-acetyl-1,3-indandionate; ISOVIND, 2-isovaleryl-1,3-indandionate; and BIND, 2-benzoyl-1,3-indandionate, respectively. These devices exhibited photo and electroluminescent emissions. An important characteristic presented by devices is that their electroluminescent (EL) spectra, in the region of 5 D 0 → 7 F J ( J = 0, 1, 2, 3 and 4) transitions of Eu 3+ ion, show profiles that are different from photoluminescent (PL) ones. In addition to narrow bands arising from intraconfigurational-4f 6 transitions, devices 1 and 2 also exhibited a broad band with maximum at around 500 nm which is assigned to electrophosphorescence from the indandionate ligands. On the other hand, EL spectra of device 3 present only narrow bands from 5 D 0 → 7 F J transitions. [Eu(ACIND) 3 (TPPO) 2 ] complexes are promising candidates to prepare efficient organic light-emitting devices (OLEDs) when compared with those containing Eu 3+ -complexes of aliphatic β-diketonate anions.
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Research context
OpenAlex topics: Lanthanide and Transition Metal Complexes · Organic Light-Emitting Diodes Research · Magnetism in coordination complexes
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (22)
Show source-provided references
1. Colle · J. Lumin. · 2004 · 110 · 20010.1016/j.jlumin.2004.08.009 ↗
2. Kim · Sci. Technol. Adv. Mater. · 2004 · 5 · 33110.1016/j.stam.2003.11.009 ↗
3. H.A. Al Attar, A.P. Monkman, M. Tavasli, S. Bettington, M.R. Bryce, Appl. Phys. Lett. 86 (2005) Art. No. 121101.10.1063/1.1873046 ↗
4. Ling · J. Mater. Chem. · 2004 · 14 · 274110.1039/b405873a ↗
5. Kido · Chem. Rev. · 2002 · 102 · 235710.1021/cr010448y ↗
6. Bemquerer · J. Inorg. Biochem. · 2002 · 91 · 36310.1016/S0162-0134(02)00445-2 ↗
7. Hemmila · J. Fluoresc. · 2005 · 15 · 52910.1007/s10895-005-2826-6 ↗
8. de Sá · Coord. Chem. Rev. · 2000 · 196 · 16510.1016/S0010-8545(99)00054-5 ↗
9. Niyama · Spectrochim. Acta – Part A · 2005 · 61 · 264310.1016/j.saa.2004.10.006 ↗
10. Kim · Opt. Mater. · 2002 · 21 · 18110.1016/S0925-3467(02)00133-7 ↗
11. Yu · Inorg. Chem. · 2005 · 44 · 161110.1021/ic0485561 ↗
12. Gerasimenko · Dokl. Akad. Nauk. SSSR · 1984 · 278 · 117
13. Poluektov · Zh. Neorg. Khim. · 1982 · 27 · 2242
14. Vitkun · Dokl. Akad. Nauk. SSSR. · 1981 · 260 · 1367
15. Teotonio · Polyhedron · 2006 · 25 · 348810.1016/j.poly.2006.06.035 ↗
16. Adachi · J. Appl. Phys. · 2000 · 87 · 804910.1063/1.373496 ↗
17. Reyes · Thin Solid Films · 2004 · 469 · 5910.1016/j.tsf.2004.06.184 ↗
18. Reyes · Chem. Phys. Lett. · 2004 · 396 · 5410.1016/j.cplett.2004.07.074 ↗
19. Silva · J. Alloys Compounds · 2001 · 323 · 33610.1016/S0925-8388(01)01033-7 ↗
20. Longo · Chem. Phys. Lett. · 2000 · 328 · 6710.1016/S0009-2614(00)00898-8 ↗
21. Auzel · Revue de Physique Appliquee · 1985 · 20 · 27310.1051/rphysap:01985002005027300 ↗
22. Micaroni · J. Solid State Electrochem. · 2002 · 7 · 5510.1007/s10008-002-0289-0 ↗