TY - JOUR
T1 - Thermally activated delayed fluorescence from 3n π ∗ to 1n π∗ up-conversion and its application to organic light-emitting diodes
AU - Li, Jie
AU - Zhang, Qisheng
AU - Nomura, Hiroko
AU - Miyazaki, Hiroshi
AU - Adachi, Chihaya
N1 - Publisher Copyright:
© 2014 AIP Publishing LLC.
PY - 2014/7/7
Y1 - 2014/7/7
N2 - Intense nπ∗ fluorescence from a nitrogen-rich heterocyclic compound, 2,5,8-tris(4-fluoro-3-methylphenyl)-1,3,4,6,7,9,9b-heptaazaphenalene (HAP-3MF), is demonstrated. The overlap-forbidden nature of the nπ∗ transition and the higher energy of the 3ππ∗ state than the 3nπ∗ one lead to a small energy difference between the lowest singlet (S1) and triplet (T1) excited states of HAP-3MF. Green-emitting HAP-3MF has a moderate photoluminescence quantum yield of 0.26 in both toluene and doped film. However, an organic light-emitting diode containing HAP-3MF achieved a high external quantum efficiency of 6.0%, indicating that HAP-3MF harvests singlet excitons through a thermally activated T1 → S1 pathway in the electroluminescent process.
AB - Intense nπ∗ fluorescence from a nitrogen-rich heterocyclic compound, 2,5,8-tris(4-fluoro-3-methylphenyl)-1,3,4,6,7,9,9b-heptaazaphenalene (HAP-3MF), is demonstrated. The overlap-forbidden nature of the nπ∗ transition and the higher energy of the 3ππ∗ state than the 3nπ∗ one lead to a small energy difference between the lowest singlet (S1) and triplet (T1) excited states of HAP-3MF. Green-emitting HAP-3MF has a moderate photoluminescence quantum yield of 0.26 in both toluene and doped film. However, an organic light-emitting diode containing HAP-3MF achieved a high external quantum efficiency of 6.0%, indicating that HAP-3MF harvests singlet excitons through a thermally activated T1 → S1 pathway in the electroluminescent process.
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U2 - 10.1063/1.4887346
DO - 10.1063/1.4887346
M3 - Article
AN - SCOPUS:84908502631
SN - 0003-6951
VL - 105
JO - Applied Physics Letters
JF - Applied Physics Letters
IS - 1
M1 - 013301
ER -