系统间交叉
有机发光二极管
光电子学
准分子
材料科学
窄带
二极管
量子效率
费斯特共振能量转移
亮度
能量转移
荧光
寄主(生物学)
锗
量子点
能量(信号处理)
高效能源利用
能量转换效率
作者
Xu Zhang,Zhanxiang Chen,Manli Huang,Jiahui Liu,siyuan he,Cheng Zhong,Jingsheng Miao,Xue Zhou,Yu Gu,Chuluo Yang
标识
DOI:10.1038/s41467-026-76914-5
摘要
Abstract Multi-resonance thermally activated delayed fluorescence (MR-TADF) materials open a heavy-metal-free avenue toward highly efficient, narrowband organic light-emitting diodes (OLEDs). However, their slow reverse intersystem crossing (RISC) kinetics lead to severe efficiency roll-off at practical driving currents, and existing strategies to improve RISC often require emitter-specific chemical modifications. Here we demonstrate a general strategy by integrating heavy-atom germanium into hole-transporting/electron-transporting hosts to construct an exciplex system that accelerates spin-flip dynamics. This design enhances RISC rates in diverse MR-TADF emitters via Förster resonance energy transfer without altering their electronic structure. The resulting blue and green OLEDs achieve external quantum efficiencies exceeding 40% with markedly suppressed efficiency roll-off relative to silicon-based counterparts. Notably, the green device exhibits a half-lifetime of 241 h at an initial luminance of 1,000 cd m -2 , surpassing previously reported OLEDs employing non-metallic heavy atoms. This general host-guest strategy advances MR-TADF systems toward practical high-performance displays.
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