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Bis(diphenylamino)-9,9′-spirobifluorene functionalized Ir(iii) complex: a conceptual design en route to a three-in-one system possessing emitting core and electron and hole transport peripherals
Author(s) -
HsiaoFan Chen,
KenTsung Wong,
YiHung Liu,
Yu Wang,
Yi Cheng,
Min-Wen Chung,
PiTai Chou,
HaiChing Su
Publication year - 2010
Publication title -
journal of materials chemistry
Language(s) - English
Resource type - Journals
eISSN - 1364-5501
pISSN - 0959-9428
DOI - 10.1039/c0jm02097d
Subject(s) - chromophore , quantum yield , luminescence , yield (engineering) , electron , quantum efficiency , chemistry , photochemistry , oled , ligand (biochemistry) , materials science , optoelectronics , physics , fluorescence , quantum mechanics , organic chemistry , biochemistry , receptor , layer (electronics) , metallurgy
Conceptual design of a three-in-one (luminescence chromophore with electron and hole transports) system was demonstrated by a functionalized Ir(III) complex 3, in which 4,5-diazafluorene and bis(diphenylamino) serve as electron and hole transporting sites, respectively. The poor emission quantum yield of 3 was systematically examined via a series of photophysical studies in combination with theoretical approaches. The far lifting of the π-electron from -NPh2 renders virtually no 3MLCT contribution to the lowest transition in the triplet manifold as compared with that of the parent model 2 without amino substituents. With an empirical approach, we conclude that an energy gap law may account for the major deactivation process. A light-emitting electrochemical cell (LEC) device based on 3 shows peak EQE, peak current efficiency and peak power efficiency at 2.4 V of 0.020%, 0.013 cd A−1 and 0.017 lm/W, respectively. The low device efficiencies are in accordance with the low PL quantum yield, stemming from the ligand-centered radiationless deactivation. The conceptual design presented here should provide valuable information for future progress en route to an ideal three-in-one system suited for OLEDs.

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