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High triplet energy bipolar host materials with the combination of dibenzofuran and benziimidazobenzoimidazole moieties for blue thermally activated delayed fluorescence emitter
Journal of Materials Chemistry C ( IF 6.4 ) Pub Date : 2020-09-11 , DOI: 10.1039/d0tc02884c
Kyu Man Youn 1, 2, 3, 4, 5 , Hyuna Lee 1, 2, 3, 4, 5 , Han Jong Yoo 1, 2, 3, 4, 5 , Young Hun Jung 1, 2, 3, 4, 5 , Jae Do Park 1, 2, 3, 4, 5 , Hyein Jeong 5, 6, 7, 8 , Jungsub Lee 5, 6, 7, 8 , Ju Young Lee 1, 2, 3, 4, 5 , Jang Hyuk Kwon 1, 2, 3, 4, 5
Affiliation  

Two bipolar host materials were designed and synthesized for blue thermally activated delayed fluorescence (TADF) OLEDs. Both bipolar materials, 5-(4-(dibenzo[b,d]furan-2-yl)-pyridin-2-yl)-5H-benzo[d]benzo-[4,5]imidazo[1,2-a]imidazole (4-DBFBI) and 5-(5-(dibenzo[b,d]furan-2-yl)-pyridin-2-yl)-5H-benzo[d]benzo-[4,5]imidazo[1,2-a]imidazole (5-DBFBI), were constructed with a hole-transporting type of benzimidazole moiety and an electron-transporting type of dibenzofuran moiety, and these derivatives exhibit high triplet energy over 3.10 eV. To achieve a high triplet energy level, a pyridine linker was placed between the benzimidazole and dibenzofuran moieties. As a result, 4-DBFBI and 5-DBFBI showed a high triplet energy level of 3.06 eV and 2.96 eV, respectively. Further, blue TADF devices were fabricated with our synthesized bipolar host materials. For our current study, we adopted 5,10-diphenyl-15-(10-(2,4,6-triisopropylphenyl)-10H-dibenzo[b,e][1,4]oxaborinin-3-yl)-10,15-dihydro-5H-diindolo[3,2-a:3′,2′-c]carbazole (PXB-DI) as the blue TADF dopant. The maximum external quantum efficiencies of the 20 wt% blue TADF devices were 31.8 and 32.5% for 4-DBFBI and 5-DBFBI, respectively. Moreover, the 4-DBFBI based host device exhibited a very low efficiency roll-off of 0.93 up to 1000 cd m−2, which is attributed to its well-balanced charge transporting ability.

中文翻译:

高三重态能量双极主体材料,结合二苯并呋喃和苯并咪唑并苯并咪唑部分,用于蓝色热激活的延迟荧光发射体

设计并合成了两种双极性主体材料,用于蓝色热激活延迟荧光(TADF)OLED。两种双极材料,5-(4-(二苯并[ bd ]呋喃-2-基)-吡啶-2-基)-5 H-苯并[ d ]苯并-[4,5]咪唑[1,2- a ]咪唑(4-DBFBI)和5-(5-(二苯并[ bd ]呋喃-2-基)-吡啶-2-基)-5 H-苯并[ d ]苯并-[4,5]咪唑[1,2- a用咪唑(5-DBFBI)空穴传输型苯并咪唑部分和电子传输型二苯并呋喃部分构建,这些衍生物在3.10 eV以上显示出高三重态能量。为了获得高的三线态能量水平,将吡啶连接基置于苯并咪唑和二苯并呋喃部分之间。结果,4-DBFBI和5-DBFBI分别显示出3.06 eV和2.96 eV的高三重态能级。此外,蓝色TADF器件是用我们合成的双极主体材料制造的。在我们当前的研究中,我们采用了5,10-二苯基-15-(10-(2,4,6-三异丙基苯基)-10 H-二苯并[ be ] [1,4] oxaborinin-3-yl)-10 ,15-dihydro-5 H -diindolo [3,2- a:3',2'- c]咔唑(PXB-DI)作为蓝色TADF掺杂剂。对于4-DBFBI和5-DBFBI,20 wt%蓝色TADF器件的最大外部量子效率分别为31.8和32.5%。此外,基于4-DBFBI的主机设备在1000 cd m -2时表现出0.93的非常低的效率下降,这归因于其良好平衡的电荷传输能力。
更新日期:2020-10-16
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