کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1671714 | 1008922 | 2008 | 5 صفحه PDF | دانلود رایگان |

In this paper the synthesis, photoluminescence and electroluminescence investigation of the novel tetrakis β-diketonate of rare-earth complexes such as, M[Eu(dbm)4] and M[Tb(acac)4] with a variety of cationic ligands, M = Li+, Na+ and K+ have been investigated. The emission spectra of the Eu3+ and Tb3+ complexes displayed characteristic narrow bands arising from intraconfigurational transitions of trivalent rare-earth ions and exhibited red color emission for the Eu3+ ion (5D0→7FJ, J = 0–6) and green for the Tb3+ ion (5D4→7FJ, J = 6–0). The lack of the broaden emission bands arising from the ligands suggests the efficient intramolecular energy transfer from the dbm and acac ligands to Eu3+ and Tb3+ ions, respectively. In accordance to the expected, the values of PL quantum efficiency (η) of the emitting 5D0 state of the tetrakis(β-diketonate) complexes of Eu3+ were higher compared with those tris-complexes. Therefore, organic electroluminescent (EL) devices were fabricated with the structure as follows: indium tin oxide (ITO)/hole transport layer (HTL) NPB or MTCD/emitter layer M[RE(β-diketonate)4] complexes)/Aluminum (Al). All the films were deposited by thermal evaporation carried out in a high vacuum environment system. The OLED light emission was independent of driving voltage, indicating that the combination of charge carriers generates excitons within the M[RE(β-diketonate)4] layers, and the energy is efficiently transferred to RE3+ ion. As a best result, a pure red and green electroluminescent emission was observed from the Eu3+ and Tb3+ devices, confirmed by (X,Y) color coordinates.
Journal: Thin Solid Films - Volume 517, Issue 3, 1 December 2008, Pages 1096–1100