Highly efficient deep-blue organic light-emitting diodes based on pyreno[4,5-d]imidazole-anthracene structural isomers

被引:45
|
作者
Liu, Hui [1 ]
Kang, Liangliang [2 ]
Li, Jinyu [1 ]
Liu, Futong [1 ]
He, Xin [1 ]
Ren, Shenghong [1 ]
Tang, Xiangyang [1 ]
Lv, Changli [2 ]
Lu, Ping [1 ]
机构
[1] Jilin Univ, State Key Lab Supramol Struct & Mat, Qianjin St 2699, Changchun 130012, Jilin, Peoples R China
[2] Northeast Normal Univ, Fac Chem, Changchun 130024, Jilin, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
ACTIVATED DELAYED FLUORESCENCE; AGGREGATION-INDUCED EMISSION; ELECTROLUMINESCENCE; OLEDS; PERFORMANCE; DEVICES; DESIGN; FLUOROPHORES; DERIVATIVES; MOLECULES;
D O I
10.1039/c9tc02990g
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
High-efficiency deep-blue luminophores, especially those satisfying the National Television Standards Committee (NTSC) blue standard Commission Internationale de l'eclairage (CIE) coordinates of (0.14, 0.08), are vital for full-color displays and solid-state illumination. However, deep-blue luminescent materials with efficient photoluminescence quantum yields (phi(PL)s) and high external quantum efficiencies (EQEs) over 5% remain very limited. Imidazole has shown great potential in optoelectronic fields owing to its ambipolar nature. Combining imidazole with rigid aromatic rings, such as naphthalene, phenanthrene and pyrene, could effectively enlarge the pi-electronic delocalization, reduce non-radiative transitions of molecules and ensure high phi(PL)s in the solid-state. Herein, two symmetrically twisted pyreno[4,5-d]imidazole-anthracene structural isomers, 9,10-bis(4-(10-phenyl-9H-pyreno[4,5-d]imidazol-9-yl)phenyl)anthracene (N-BPyIA) and 9,10-bis(4-(9-phenyl-9H-pyreno[4,5-d]imidazol-10-yl)phenyl)anthracene (C-BPyIA), have been designed and synthesized by connecting one anthracene group with two pyreno[4,5-d]imidazole groups at the N1 and the C2 position, respectively. They both show high phi(PL)s in neat films (46% for N-BPyIA and 54% for C-BPyIA), good thermal stabilities (T-d > 541 degrees C), and appropriate energy levels for carrier injection. N-BPyIA shows better performance than C-BPyIA when applied in OLEDs. The non-doped device based on N-BPyIA shows sky blue emission with CIE coordinates of (0.22, 0.31), achieving a high EQE of 5.63% with a low efficiency roll-off. In particular, a doped device with better performance is further realized, providing an EQE of 7.67% and deep-blue emission (CIE (0.15, 0.10)), which is very close to the NTSC standard. Such high OLED efficiency may be ascribed to triplet energy harvesting by triplet-triplet annihilation. And to our best knowledge, this is one of the best outcomes of deep-blue imidazole-based fluorescent OLEDs. The results also pave the way for a new type of high-efficiency deep-blue organic luminescent materials regulated by structural isomerization.
引用
收藏
页码:10273 / 10280
页数:8
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