Abstract
Highly efficient and stable narrowband blue organic light-emitting diodes (OLEDs) are vital for high-definition displays, yet the achievement of such devices via a concise binary-doped fabrication architecture remains challenging. Herein, an effective and robust single-component host matrix with a spatial bipolarity configuration is developed for high-performance OLEDs. Two elaborately designed molecules are constructed on a non-conjugated silyl linker connecting boron–oxygen and carbazole-derived groups. The boron–oxygen electron-accepting and carbazole-based electron-donating moieties exhibit synergistic and complementary group functions, achieving wide bandgaps of excited energy states, along with thermally activated delayed fluorescence and bipolar carrier transport features. Following the incorporation of a blue multiresonant guest emitter, the doped emissive film showcases enhanced horizontal orientation and photoluminescent efficiency. The binary-doped narrowband blue OLEDs achieve the record maximum external quantum efficiency of 42.3% with low roll-off (efficiency of 38.3% at 1,000 cd m−2), and the improved operational stability with a half-lifetime of 3076 h at an initial luminance of 100 cd m−2. This study reveals that the utilization of a spatial bipolarity host matrix is a promising approach to realize narrowband blue OLEDs with concise architecture and high performance.
| Original language | English |
|---|---|
| Journal | Angewandte Chemie - International Edition |
| DOIs | |
| State | Accepted/In press - 2025 |
Keywords
- High efficiency and stability
- Narrowband blue device
- Single-component matrix
- Spatial bipolarity
- Thermally-activated delayed fluorescence