TY - JOUR
T1 - Deep Blue Emitter Based on Tris(triazolo)triazine Moiety with CIEy < 0.08 for Highly Efficient Solution-Processed Organic Light-Emitting Diodes Via Molecular Strategy of “Hot Excitons”
AU - Zeng, Songkun
AU - Xiao, Chen
AU - Zhou, Jiachun
AU - Dong, Qiwei
AU - Li, Qiuying
AU - Lim, Junseop
AU - Ma, Huili
AU - Lee, Jun Yeob
AU - Zhu, Weiguo
AU - Wang, Yafei
N1 - Publisher Copyright:
© 2022 Wiley-VCH GmbH.
PY - 2022/5/13
Y1 - 2022/5/13
N2 - Realizing high efficiency deep blue emission with a Commission international de I'Eclairage (CIE) coordinate of CIEy < 0.08 is still a big challenge. In this contribution, three molecules, named TTT-TPA-R (R = H, OMe, tBu), using tris(triazolo)triazine (TTT) as the acceptor and triphenylamine derivatives (TPA-R, R = H, OMe, and tBu) as the donor are prepared and characterized. All these emitters show deep/pure blue emission between 420 and 470 nm in the PMMA film, concomitant with the excellent emission efficiency of 80–100%. Both experimental and calculated methods demonstrate that these emitters exhibit a clearly hybridized local and charge-transfer excited state and can harvest both singlet and triplet excitons via reverse intersystem crossing process from the high-lying triplet to singlet states. Therefore, the solution processable deep blue organic light-emitting diodes (OLEDs) achieve a maximum external quantum efficiency (EQEmax) of 10.5% which is the recorded value for the solution processable deep blue OLED based on the “hot exciton” mechanism. Using TTT-TPA-H as the host material, solution-processed phosphorescent OLED based on PO-01 presents the EQEmax of 20.2%. These results pave a novel avenue for designing highly efficient deep blue emitter in solution processable OLED.
AB - Realizing high efficiency deep blue emission with a Commission international de I'Eclairage (CIE) coordinate of CIEy < 0.08 is still a big challenge. In this contribution, three molecules, named TTT-TPA-R (R = H, OMe, tBu), using tris(triazolo)triazine (TTT) as the acceptor and triphenylamine derivatives (TPA-R, R = H, OMe, and tBu) as the donor are prepared and characterized. All these emitters show deep/pure blue emission between 420 and 470 nm in the PMMA film, concomitant with the excellent emission efficiency of 80–100%. Both experimental and calculated methods demonstrate that these emitters exhibit a clearly hybridized local and charge-transfer excited state and can harvest both singlet and triplet excitons via reverse intersystem crossing process from the high-lying triplet to singlet states. Therefore, the solution processable deep blue organic light-emitting diodes (OLEDs) achieve a maximum external quantum efficiency (EQEmax) of 10.5% which is the recorded value for the solution processable deep blue OLED based on the “hot exciton” mechanism. Using TTT-TPA-H as the host material, solution-processed phosphorescent OLED based on PO-01 presents the EQEmax of 20.2%. These results pave a novel avenue for designing highly efficient deep blue emitter in solution processable OLED.
KW - deep blue emitter
KW - hot excitons
KW - reverse intersystem crossing process
KW - solution-processable OLED
KW - tris(triazolo)triazine
UR - http://www.scopus.com/inward/record.url?scp=85124549895&partnerID=8YFLogxK
U2 - 10.1002/adfm.202113183
DO - 10.1002/adfm.202113183
M3 - 文章
AN - SCOPUS:85124549895
SN - 1616-301X
VL - 32
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 20
M1 - 2113183
ER -