Two bipolar host materials p-cbtz and m-cbtz, with both phenylcarbazole and 3,5-bis(2-pyridyl)-1,2,4-triazole moieties, were synthesized and tested for fabrication of various phosphorescent OLEDs. The sp3-hybridized nitrogen atom of the 1,2,4-triazole fragment disrupted the π-conjugation between the electron donating 9-phenylcarbazole and the electron accepting 3,5-bis(2-pyridyl)-1,2,4-triazole and, thus, exhibited promising properties such as bipolar charge transport feature (10−5–10−6 cm2V−1s−1) and with relatively high triplet energy gaps (ET = 2.82–2.75 eV). As a result, they were utilized as universal hosts for various phosphorescent OLEDs, showing high efficiencies and low efficiency roll-off. For example, the devices hosted by m-cbtz achieve maximum external quantum efficiencies (ηext) of 8.8% for blue, 16.7% for green, 17.5% for yellow and 16.7% for red-emitting OLEDs. In addition, we also fabricated dual-emitter WOLEDs with a co-doped single emissive layer, exhibiting satisfactory device efficiencies (12.4%, 25 cd A−1, 17 lm W−1) and with highly stable chromaticity (CIEx = 0.26–0.27 and CIEy = 0.38) at an applied voltage of 8 to 11 V. These results demonstrated that the newly synthesized, phenylcarbazole-dipyridyl triazole host materials are advantageous for fabrication of various highly efficient phosphorescent OLEDs.
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Hung et al. (2012) studied this question.
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