Enhancement of efficiencies for tandem green phosphorescent organic light-emitting devices with a p-type charge generation layer
[Display omitted] The operating voltage of the tandem green phosphorescent organic light-emitting device with a 1,4,5,8,9,11-hexaazatriphenylene-hexacarbonitrile layer was improved by 3% over that of the organic light-emitting device with a molybdenum trioxide layer. The maximum brightness of the ta...
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Veröffentlicht in: | Materials research bulletin 2014-10, Vol.58, p.141-144 |
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The operating voltage of the tandem green phosphorescent organic light-emitting device with a 1,4,5,8,9,11-hexaazatriphenylene-hexacarbonitrile layer was improved by 3% over that of the organic light-emitting device with a molybdenum trioxide layer. The maximum brightness of the tandem green phosphorescent organic light-emitting device at 21.9V was 26,540cd/m2. The dominant peak of the electroluminescence spectra for the devices was related to the fac-tris(2-phenylpyridine) iridium emission.
•Tandem OLEDs with CGL were fabricated to enhance their efficiency.•The operating voltage of the tandem OLED with a HAT-CN layer was improved by 3%.•The efficiency and brightness of the tandem OLED were 13.9cd/A and 26,540cd/m2.•Efficiency of the OLED with a HAT-CN layer was lower than that with a MoO3 layer.
Tandem green phosphorescent organic light-emitting devices with a 1,4,5,8,9,11-hexaazatriphenylene-hexacarbonitrile or a molybdenum trioxide charge generation layer were fabricated to enhance their efficiency. Current density–voltage curves showed that the operating voltage of the tandem green phosphorescent organic light-emitting device with a 1,4,5,8,9,11-hexaazatriphenylene-hexacarbonitrile layer was improved by 3% over that of the corresponding organic light-emitting device with a molybdenum trioxide layer. The efficiency and the brightness of the tandem green phosphorescent organic light-emitting device were 13.9cd/A and 26,540cd/m2, respectively. The current efficiency of the tandem green phosphorescent organic light-emitting device with a 1,4,5,8,9,11-hexaazatriphenylene-hexacarbonitrile layer was lower by 1.1 times compared to that of the corresponding organic light-emitting device with molybdenum trioxide layer due to the decreased charge generation and transport in the 1,4,5,8,9,11-hexaazatriphenylene-hexacarbonitrile layer resulting from triplet–triplet exciton annihilation. |
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ISSN: | 0025-5408 1873-4227 |
DOI: | 10.1016/j.materresbull.2014.04.045 |