Issue 2, 2014

Solution-processed bipolar small molecular host materials for single-layer blue phosphorescent organic light-emitting diodes

Abstract

Three new solution processable small molecular host materials based on the bis-[3,5-di(9H-carbazol-9-yl)phenyl] structural moiety have been developed for blue phosphorescent (FIrpic dopant) organic light-emitting diodes. All three host materials have been characterized as having high glass transition temperatures (Tgs), 155–175 °C, indicative of good morphological stability of their amorphous thin films prepared from the solution process. Whereas N,N-bis-[3,5-di(9H-carbazol-9-yl)phenyl]methylamine (CzPAMe) has the highest solid state triplet energy gap (ET) of 2.73 eV, tetrakis-[3,3′,5,5′-(9H-carbazol-9-yl)]triphenylphosphine oxide (CzPPO) and N,N-bis-[3,5-di(9H-carbazol-9-yl)phenyl]pyrimidin-2-amine (CzPAPm) are two host materials which are potentially bipolar for charge transport due to the electron deficient units of phenylphosphine oxide and pyrimidine, respectively. Due to the insufficient ET (2.56 eV) of CzPAPm, CzPPO or CzPAMe devices are significantly better than CzPAPm devices with or without a 1,3-bis[(4-tert-butylphenyl)-1,3,4-oxadiazolyl]phenylene (OXD-7) co-host. Particularly, having no OXD-7 co-host and no vacuum thermal-deposited extra electron transporting layer, single-layer devices of CzPPO surpass CzPAMe devices and reach current efficiencies as high as 9.32 cd A−1 (or power efficiency of 4.97 lm W−1), one of the highest efficiencies among small molecular devices with the same fabrication process and same device configuration.

Graphical abstract: Solution-processed bipolar small molecular host materials for single-layer blue phosphorescent organic light-emitting diodes

Article information

Article type
Paper
Submitted
20 Aug 2013
Accepted
17 Oct 2013
First published
18 Oct 2013

J. Mater. Chem. C, 2014,2, 382-391

Solution-processed bipolar small molecular host materials for single-layer blue phosphorescent organic light-emitting diodes

Y. Lee, Y. Chang, M. Lee, P. Chiang, C. Chen and C. Chen, J. Mater. Chem. C, 2014, 2, 382 DOI: 10.1039/C3TC31641F

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