2017
DOI: 10.1039/c6tc05630j
|View full text |Cite|
|
Sign up to set email alerts
|

Bipolar hosts and non-doped deep-blue emitters (CIEy= 0.04) based on phenylcarbazole and 2-(2-phenyl-2H-1,2,4-triazol-3-yl)pyridine groups

Abstract: Four bipolar materials using 1,2,4-triazol derivative as an acceptor and carbazole as a donor were synthesized. They can be used not only as emitters to fabricate deep-blue OLEDs, but also as hosts to construct PhOLEDs.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
22
0

Year Published

2018
2018
2021
2021

Publication Types

Select...
6
1

Relationship

1
6

Authors

Journals

citations
Cited by 51 publications
(22 citation statements)
references
References 39 publications
0
22
0
Order By: Relevance
“…It is also worth noting the outstanding EQE value of the TPBCzC1-baesd OLED also represents the best results for violet-blue OLEDs with CIEy < 0.046 based on fluorescent materials ( Figure 6C and Table 2). [44][45][46][47][48][49] Moreover, all devices exhibit a very low efficiency roll-off probably because the radiative transition channels are activated and the non-radiative transition channels are inhibited in the aggregate state, confirming the excellent efficiency stabilities of the devices (Figures 6A and S7).…”
Section: Non-doped Violet-blue Oledsmentioning
confidence: 84%
“…It is also worth noting the outstanding EQE value of the TPBCzC1-baesd OLED also represents the best results for violet-blue OLEDs with CIEy < 0.046 based on fluorescent materials ( Figure 6C and Table 2). [44][45][46][47][48][49] Moreover, all devices exhibit a very low efficiency roll-off probably because the radiative transition channels are activated and the non-radiative transition channels are inhibited in the aggregate state, confirming the excellent efficiency stabilities of the devices (Figures 6A and S7).…”
Section: Non-doped Violet-blue Oledsmentioning
confidence: 84%
“…2a, the absorption of M1 and M2 exhibits bands in the range from 250 to 430 nm (247, 298, 387 nm for M1; 254, 303, 378 nm for M2), attributed to the p-p* electronic transition of the quinoxaline and carbazole unit. 33,34,[40][41][42] M1 and M2 show almost the same absorption spectra in spite of the larger p-electron conjugation of compound M2, implying that the introduction of the phenyl spacer almost has little effect on the absorption properties of these donor-acceptor systems.…”
Section: Photophysical Propertiesmentioning
confidence: 99%
“…However, the LUMO energy of compound M1 (À3.09 eV) were higher than that of M2 (À3.21 eV), implying that the phenyl spacer have evident inuence on the LUMO of these donor-acceptor systems. [40][41][42] Red phosphorescent OLEDs…”
Section: Electrochemical Propertiesmentioning
confidence: 99%
See 1 more Smart Citation
“…Majority of these reports were mainly confined to two strategies such as directly linked D‐A structure or D‐π‐A structure with a π linker. [ 6–10 ] Various acceptors such as imidazole, [ 11 ] phenanthroimidazole, [ 12–14 ] oxadiazole, [ 15 ] and borane, [ 16–18 ] and donors such as carbazole, [ 17,19 ] diphenylamine, [ 20 ] acridine, [ 21,22 ] etc. have been used for this purpose.…”
Section: Introductionmentioning
confidence: 99%