The power conversion efficiency of a device incorporating a crystalline polymer/fullerene thin film improves from 5% to 7.3% – a relative increase of 45% – when an additive, diiodohexane (DIH), is present during processing. The DIH‐processed active layer exhibits substantially enhanced polymer crystallinity and smaller fractal‐like fullerene clusters.
[reaction: see text] A series of carbazole/fluorene (CBZm-Fn) hybrids were effectively synthesized through Friedel-Crafts-type substitution of the carbazole rings. These compounds were thermally and morphologically stable host materials for OLED applications. Efficient blue phosphorescent OLEDs were obtained when employing CBZ1-F2 as the host and FIrpic as the guest.
We have synthesized two fluorene-based polymeric host materials, P1 and P2, through palladiumcatalyzed Suzuki couplings of monomers containing tetraphenylsilane and 3,6-disubstituted fluorene frameworks, respectively. The resultant copolymers exhibited high glass transition temperatures (T g g 215°C) and excellent thermal stability. The conjugation lengths of polymers P1 and P2 were effectively confined through the presence of the 3,6-linkages and silane units in the polymer skeleton. The structural features endowed these copolymers with UV-violet emissions in the solid state, together with high triplet energies (E T ) 2.60 eV), which were sufficiently high for P1 and P2 to serve as appropriate hosts for green-emitting phosphors. In the case of polymer P2, the incorporation of pendent carbazole groups increased the HOMO level markedly and balanced the rates of charge injection and transportation. Employing P2 doped with green-emitting fac-tris(2-phenylpyridine)iridium as the emissive layer, we fabricated highly efficient polymer light-emitting diodes (32 cd/A, 9.2%) that exhibited significantly enhanced EL performance relative to that of the system employing P1 (14.5 cd/A, 4.2%).
We have synthesized three novel distyrylcarbazole derivatives for use as simultaneously hole-transporting and light-emitting layers in blue light-emitting diodes. Each compound, which contains a rigid carbazole core and two 2,2-diphenylvinyl end groups substituted through either the 3,6-or the 2,7-position, forms films satisfactorily and exhibits a blue emission with its PL maximum in the range 459-470 nm. Photophysical measurements indicate that twisting of the adjacent C-C bonds in the 3,6-position of the carbazole core in dilute solutions causes an efficient nonradiative relaxation to occur, yielding a much smaller quantum yield for fluorescence in 3,6-linked carbazoles. As intense emissions of 2,7-linked carbazoles are observed, such deactivation from an excited-state is inefficient therein. Electrochemical studies revealed that incorporation of the carbazole core increased the HOMO energy effectively; this feature facilitates hole injection. These distyrylcarbazole derivatives are promising bifunctional, blue-emitting, holetransporting molecules for use in simple double-layer devices of a general structure ITO/emitting layer/TPBI/Mg : Ag, in which TPBI-1,3,5-tris(N-phenylbenzimidazol-2-yl)benzene-serves as a hole-blocking and electron-transporting material. The devices prepared using 2,7distyrylcarbazole as the emitter produced bright blue emissions having activating voltages below 3.0 V. A DPVTCz-based device attained a luminance efficiency of 3.11 cd A 21 at 5 V, a brightness of 3062 cd m 22 , and CIE color coordinates of (0.14, 0.22).
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