Triptycene derivatives as high-Tg host materials for various electrophosphorescent devices

被引:55
作者
Chou, Ho-Hsiu [1 ]
Shih, Hung-Hsin [1 ]
Cheng, Chien-Hong [1 ]
机构
[1] Natl Tsing Hua Univ, Dept Chem, Hsinchu 30013, Taiwan
关键词
BLUE ORGANIC ELECTROPHOSPHORESCENCE; LIGHT-EMITTING-DIODES; RED PHOSPHORESCENT OLEDS; ENERGY-TRANSFER; TRIPLET ENERGY; EFFICIENT; CARBAZOLE; COMPLEXES; MOLECULES; TRANSPORT;
D O I
10.1039/b918188a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We have synthesized three triptycene derivatives, TCTP (2,6,14-triscarbazolyltriptycene), TATP (2,6,14-tris-(diphenylamino) triptycene) and TPOTP (2,6,14-tris(diphenylphosphoryl) triptycene) which show very high triplet energy gaps (2.94-3.15 eV) and glass transition temperatures (T(g)s) >= 170 degrees C. The HOMO and LUMO levels of these three materials indicate that TCTP and TATP possess hole transport characteristics, while TPOTP has electron transport characteristics. These carrier-transporting properties are further supported by the current density-voltage characteristics of the hole-only and electron-only devices of the materials. TATP could be employed as a general host for blue, green and red electrophosphorescence devices providing high brightness, and good current and power efficiencies. The devices using TCTP and TPOTP as the host for the phosphorescence emitter FIrpic showed maximum external quantum efficiencies as high as 10.1% and 16.9%, respectively. By using a blend of TCTP and TPOTP as blue co-host for FIrpic (iridium(III) bis(4,6-difluorophenylpyridinato) picolinate), the device shows an external quantum efficiency of 15.5% at 4.5 V, current efficiency (eta(c)) of 31.9 cd A(-1) at 4.5 V, power efficiency (eta(p)) of 25.1 lm/W at 4.0 V, respectively. The co-host system greatly improves the performance of the device at normal operation brightness due to the decrease of driving voltage and the balance of hole and electron transport in the device.
引用
收藏
页码:798 / 805
页数:8
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