| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1264330 | Organic Electronics | 2015 | 9 Pages |
•Two novel 1,2,4-thiadiazole derivatives were synthesized for green PhOLED hosts.•By tuning transport mobility, hosts from bipolar to electron-type were realized.•High efficiency green EL device were fabricated by employing these two hosts.
Two novel host materials, from bipolar-type BzCzTHZ (5-(2-(9H-carbazol-9-yl)phenyl)-3-(3-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenyl)-1,2,4-thiadiazole) to electron-type DBzTHZ (3,5-bis(3-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenyl)-1,2,4-thiadiazole), were designed and synthesized utilizing the unsymmetric intermediate of 3-bromo-5-chloro-1,2,4-thiadiazole as the center. Their thermal, photoelectronic, energy levels, charge transport mobility properties can be easily tuned by changing the radio of benzimidazole/carbazole moieties. Using a common device structure ITO/MoO3 (10 nm)/TAPC (50 nm)/TCTA (5 nm)/host: Ir(ppy)3 (3 wt%) (20 nm)/TmPyPB (45 nm)/LiF (1 nm)/Al (100 nm), highly efficient green electrophosphorescent devices were successfully achieved. Devices hosted by DBzTHZ and BzCzTHZ achieved maximum power efficiencies (ηp, max) of 95.2 and 86.2 lm/W, corresponding to maximum quantum efficiency (ηEQE, max) of 23.4 and 22.2%, respectively. Moreover, the electron-type host DBzTHZ based device exhibits an ideal turn-on voltage (2.5 V at 1.0 cd/m2). These results demonstrate that electron-type hosts are competitive with bipolar hosts.
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