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1.Institute of Materials Research, Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China
2.Department of Chemistry, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan
3.Center for Organic Photonics and Electronic Research (OPERA), Kyushu University, Fukuoka 819-0395, Japan
Chengcheng Wu (wucc@tsinghua.edu.cn)
Feiyu Kang (fykang@sz.tsinghua.edu.cn)
Chihaya Adachi (adachi@cstf.kyushu-u.ac.jp)
Takuji Hatakeyama (hatake@kuchem.kyoto-u.ac.jp)
Guodan Wei (weiguodan@sz.tsinghua.edu.cn)
Received:28 July 2025,
Revised:2026-01-11,
Accepted:01 March 2026,
Online First:02 June 2026,
Published:31 August 2026
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Li, S. Q. et al. High-efficiency and stable deep-blue iridium phosphorescent OLEDs with enhanced charge transfer dynamics. Light: Science & Applications, 15, 2858-2870 (2026).
Li, S. Q. et al. High-efficiency and stable deep-blue iridium phosphorescent OLEDs with enhanced charge transfer dynamics. Light: Science & Applications, 15, 2858-2870 (2026). DOI: 10.1038/s41377-026-02264-y.
Deep-blue phosphorescent OLEDs (Ph-OLEDs) with high efficiency and stability are essential for advanced display technologies
ensuring sharp image quality and enhanced visibility. In this work
we report a novel class of asymmetric [3 + 2 +
1
]
coordinated iridium(Ⅲ) complexes incorporate strongly electron-withdrawing trifluoromethyl (–CF
3
) and fluorine (–F) modified N-heterocyclic carbene ligands. This strategic molecular design enables efficient deep-blue emission. Among these complexes
the CF
3
-substituted Ir(Ⅲ) complex (
CF
3
-2
) exhibits pronounced charge-transfer (CT) characteristics and a significantly enhanced radiative decay rate (
$$ {k}_{r} $$
= 1.28 ×10
6
s
-1
)
enabling rapid and efficient phosphorescence at 443 nm. Devices employing
CF
3
-2
demonstrated exceptional maximum external quantum efficiency (
EQE
max
) of up to 29.0%
with emission centered at 443 nm and Commission Internationale de L’Éclairage (CIE) coordinates of (0.147
0.089)
fulfilling National Television System Committee (NTSC) blue standards for high-quality displays. Meanwhile
devices employing
CF
3
-1
reached an
EQE
max
of 24.6% with a maximum luminance of 6542 cd m
−2
and CIE
x
y
of (0.152
0.126)
demonstrating high color purity and efficiency. A control device fabricated without sensitization using
CF
3
-1
further confirms its intrinsic material stability by exhibiting a remarkable operational lifetime of LT
50
of 3875 h at L = 100 cd m
−2
with CIE
x
y
of (0.132
0.131). Furthermore
hyper-OLEDs were developed using these complexes as phosphorescent sensitizers. The hyper-OLED incorporating
CF
3
-1
with the TADF emitter
v
-DABNA achieved an impressive device lifetime of LT
50
= 2127 h at 100 cd m
−2
. In parallel
the
CF
3
-2
-sensitized hyper-OLED u
sing DOB2-DABNA-A achieved a deep-blue emission with CIE coordinates of (0.146
0.067) and a lifetime of LT
50
= 373 h under the same luminance
representing a significant advancement in the practical stability of deep-blue OLEDs. Notably
we demonstrate the successful integration of these deep-blue Ph-OLEDs with OLED-on-TFT microdisplay technology
achieving a pixel resolution of 94 PPI (270 × 270 μm) with programmable emission patterns. This innovative molecular coordination design strategy provides valuable insights into ligand engineering and exciton management
opening new pathways toward high-efficiency
long-lifetime deep-blue OLEDs for next-generation microdisplay and display technologies.
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