TY - JOUR
T1 - Highly efficient nondoped blue organic light-emitting diodes based on anthracene-triphenylamine derivatives
AU - Tao, Silu
AU - Zhou, Yechun
AU - Lee, Chun-Sing
AU - Lee, Shuit-Tong
AU - Huang, Da
AU - Zhang, Xiaohong
PY - 2008/9/18
Y1 - 2008/9/18
N2 - Blue light-emitting anthracene derivatives end-capped with triphenylamine for efficient hole transportation have been designed and synthesized using two-step Suzuki coupling reactions. The compounds possess high glass transition temperatures for good thermal stability and strong blue emission in solution. Typical three-layer organic light-emitting devices (OLEDs) made from these compounds show highly efficient blue emission, which are better than or comparable to state-of-the-art fluorescent OLEDs performance. For example, 9-pyrenyl-10-(4-triphenylamine) anthrancene (PAA)-based nondoped device exhibits efficient blue emission with a maximum efficiency up to 7.9 cd/A (or 6.8 lm/W). Based on the good hole transport of the anthracene-triphenylamine derivatives, deep blue emitting devices with high efficiency were achieved by using the derivatives as both emitter and hole transporter. © 2008 American Chemical Society.
AB - Blue light-emitting anthracene derivatives end-capped with triphenylamine for efficient hole transportation have been designed and synthesized using two-step Suzuki coupling reactions. The compounds possess high glass transition temperatures for good thermal stability and strong blue emission in solution. Typical three-layer organic light-emitting devices (OLEDs) made from these compounds show highly efficient blue emission, which are better than or comparable to state-of-the-art fluorescent OLEDs performance. For example, 9-pyrenyl-10-(4-triphenylamine) anthrancene (PAA)-based nondoped device exhibits efficient blue emission with a maximum efficiency up to 7.9 cd/A (or 6.8 lm/W). Based on the good hole transport of the anthracene-triphenylamine derivatives, deep blue emitting devices with high efficiency were achieved by using the derivatives as both emitter and hole transporter. © 2008 American Chemical Society.
UR - http://www.scopus.com/inward/record.url?scp=53149117039&partnerID=8YFLogxK
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-53149117039&origin=recordpage
U2 - 10.1021/jp803957p
DO - 10.1021/jp803957p
M3 - RGC 21 - Publication in refereed journal
SN - 1932-7447
VL - 112
SP - 14603
EP - 14606
JO - The Journal of Physical Chemistry C
JF - The Journal of Physical Chemistry C
IS - 37
ER -