|Molecular weight||537.65 g/mol|
|Absorption||λmax 270 nm in DCM|
|Fluorescene||λem 380 nm in DCM|
|HOMO/LUMO||HOMO = 6.5 eV, LUMO = 3.0 eV; T1 = 2.80 eV |
|Classification / Family||Triazine, TADF blue emitter materials, TADF host materials, Phosphorescent organic light-emitting devices (PHOLEDs), Sublimed materials|
|Purity||Sublimed >99.8% (HPLC)|
|Melting point||TGA: >300 °C (0.5% weight loss)|
*Sublimation is a technique used to obtain ultra pure-grade chemicals. For more details about sublimation, please refer to the Sublimed Materials for OLED devices page.
2,4,6-tris(biphenyl-3-yl)-1,3,5-triazine (T2T) is a family member of triazine. It has one electron-withdrawing triazine core and three electron-rich biphenyl groups. It has been widely used as a host material for phosphorescent OLEDs and electron transport layer material (ETL) for TADF-OLEDs.
Due to its electron-deficient nature, T2T and its derivatives are also used as acceptor materials to form exciplexes in blue-emission TADF devices.
|Device structure||ITO/PEDOT:PSS/a-NPD (20 nm)/TCTA (5 nm)/(PPy)2Ir(acac):T2T (25 nm)/TPBi (50 nm)/LiF (0.5 nm)/Al (100 nm) |
|Max. Power Efficiency||65.2 Im/W|
|Device structure||ITO/MoO3 (3 nm)/TAPC (25 nm)/TAPC:T2T (15 nm)/T2T (5 nm)/Bphen (30 nm)/LiF (1 nm)/Al (100 nm) |
|Max. Current Efficiency||40.4 cd/A|
|Max. Power Efficiency||42.2 Im/W|
|Device structure||ITO/TAPC (35 nm)/1 wt%-TBRb:25 wt%-PXZ-TRX:mCBP (30 nm)/T2T (10 nm)/Alq3 (55 nm)/LiF (0.8 nm)/Al (100 nm) |
|Max. Current Efficiency||60 cd/A|
|Max. Power Efficiency||58 Im/W|
|Device structure||ITO (100 nm)/HAT-CN (10 nm)/TAPC (30 nm)/0.65mol%-TBRb:6.3mol%-4CzIPN-Me:mCBP (30 nm)/T2T (10 nm)/Alq3 (55 nm)/LiF (0.8 nm)/Al (100 nm) |
|Max. Current Efficiency||73 cd/A|
Literature and Reviews
- Operational stability enhancement in organic light-emitting diodes with ultrathin Liq interlayers, D. Tsang et al., Sci. Rep., 6:22463 (2016); DOI: 10.1038/srep22463.
1,3,5-Triazine derivatives as new electron transport–type host materials for
highly efficient green phosphorescent OLEDs, H-F. Chen et al., J. Mater. Chem., 19, 8112–8118 (2009); DOI: 10.1039/b913423a.
- Thermally activated delayed-fluorescence organic light-emitting diodes based on exciplex emitter with high efficiency and low roll-off, T. Lin et al., Org. Electronics, 38, 69-73 (2016); DIO: 10.1016/j.orgel.2016.08.001.
- High-efficiency organic light-emitting diodes with fluorescent emitters, H. Nakanotani et al., Nat. Commun., 5:4016 (2014); DOI: 10.1038/ncomms5016.
- Dual enhancement of electroluminescence efficiency and operational stability by rapid upconversion of triplet excitons in OLEDs, T. Furukawa1 et al., Sci. Rep., 5:8429 (2015) DOI: 10.1038/srep08429