Sato Keigo, Shizu Katsuyuki, Yoshimura Kazuaki, Kawada Atsushi, Miyazaki Hiroshi, Adachi Chihaya
Center for Organic Photonics and Electronics Research (OPERA), Kyushu University, 744 Motooka, Nishi, Fukuoka 819-0395, Japan.
Basic Research Laboratories, Nippon Steel Chemical Co., Ltd., 46-80 Nakabaru, Sakinohama, Tobata, Kitakyushu, Fukuoka 804-8503, Japan.
Phys Rev Lett. 2013 Jun 14;110(24):247401. doi: 10.1103/PhysRevLett.110.247401. Epub 2013 Jun 10.
We demonstrate an organic molecule with an energy gap between its singlet and triplet excited states of almost zero (ΔE(ST) ∼ 0 eV). Such separation was realized through proper combination of an electron-donating indolocarbazole group and a diphenyltriazine electron-accepting moiety. Calculated and measured ΔE(ST) were 0.003 and 0.02 eV, respectively. A total photoluminescence efficiency of 59% ± 2% with 45% ± 2% from a delayed component and 14% ± 2% from a prompt component was obtained for a doped film. Organic light emitting diodes containing this molecule as an emitting dopant exhibited an unexpectedly high external electroluminescence efficiency of η(EQE) = 14% ± 1%.
我们展示了一种有机分子,其单重态和三重态激发态之间的能隙几乎为零(ΔE(ST) ∼ 0 eV)。这种分离是通过给电子的吲哚并咔唑基团和二苯基三嗪电子接受部分的适当组合实现的。计算得到的和测量得到的ΔE(ST)分别为0.003 eV和0.02 eV。对于掺杂薄膜,获得了59% ± 2%的总光致发光效率,其中延迟成分占45% ± 2% , 即时成分占14% ± 2%。含有这种分子作为发光掺杂剂的有机发光二极管表现出意外高的外部电致发光效率,η(EQE) = 14% ± 1%。