TY - JOUR
T1 - Asymmetric steric-hindrance donor engineering enables ACQ-suppressed MR-TADF emitters for high-efficiency narrowband OLEDs
AU - Shi, Chengxiang
AU - Gong, Ya-Rong
AU - Jin, Jia-Ming
AU - Li, Yan
AU - Zhong, Li-Ting
AU - Liu, Xiao-Long
AU - Zhuang, Jun-Hua
AU - Shan, Shao-Liang
AU - Jiao, Xuechen
AU - Tan, Ji-Hua
AU - Huo, Yanping
AU - Zhu, Ze-Lin
AU - Chen, Wen-Cheng
PY - 2026/2/2
Y1 - 2026/2/2
N2 - A new organic emitter, mPhCz-QAO, was designed and synthesized through an asymmetric steric-hindrance donor strategy, establishing a distinctive molecular-engineering approach for achieving both high efficiency and narrowband emission in organic light-emitting materials. By introducing a meta-position asymmetric bulky donor, the strong intermolecular π-π interactions intrinsic to the QAO framework are effectively suppressed, thereby preventing aggregation-caused quenching (ACQ) in the solid state. This asymmetric donor simultaneously promotes a more delocalized distribution of the frontier molecular orbitals and strengthens the radiative transition process, leading to enhanced emission properties. Devices incorporating mPhCz-QAO exhibit exceptionally good performance at elevated doping levels, maintaining a maximum external quantum efficiency of approximately 22% as the doping concentration increases from 3 wt.% to 10 wt.%. The emission peak displays only a minimal shift (from 486 to 488 nm), while the narrow emission bandwidth of 38 nm remains fully preserved. These findings demonstrate the effectiveness of asymmetric donor engineering in overcoming concentration-related emission quenching and provide a powerful design framework for developing next-generation high-efficiency, high-color-purity organic emitters suitable for advanced display and lighting technologies. © 2026 The Authors.
AB - A new organic emitter, mPhCz-QAO, was designed and synthesized through an asymmetric steric-hindrance donor strategy, establishing a distinctive molecular-engineering approach for achieving both high efficiency and narrowband emission in organic light-emitting materials. By introducing a meta-position asymmetric bulky donor, the strong intermolecular π-π interactions intrinsic to the QAO framework are effectively suppressed, thereby preventing aggregation-caused quenching (ACQ) in the solid state. This asymmetric donor simultaneously promotes a more delocalized distribution of the frontier molecular orbitals and strengthens the radiative transition process, leading to enhanced emission properties. Devices incorporating mPhCz-QAO exhibit exceptionally good performance at elevated doping levels, maintaining a maximum external quantum efficiency of approximately 22% as the doping concentration increases from 3 wt.% to 10 wt.%. The emission peak displays only a minimal shift (from 486 to 488 nm), while the narrow emission bandwidth of 38 nm remains fully preserved. These findings demonstrate the effectiveness of asymmetric donor engineering in overcoming concentration-related emission quenching and provide a powerful design framework for developing next-generation high-efficiency, high-color-purity organic emitters suitable for advanced display and lighting technologies. © 2026 The Authors.
KW - Asymmetric
KW - Multi-resonance
KW - Organic light-emitting diodes
KW - QAO
KW - Steric hindrance donor
KW - Thermally activated delayed fluorescence
UR - http://www.scopus.com/inward/record.url?scp=105032249808&partnerID=8YFLogxK
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-105032249808&origin=recordpage
U2 - 10.1016/j.chphma.2026.01.005
DO - 10.1016/j.chphma.2026.01.005
M3 - RGC 21 - Publication in refereed journal
SN - 2772-5715
JO - ChemPhysMater
JF - ChemPhysMater
ER -