Abstract
Two blends comprising new dicyanopyrazine-based acceptors (m-CN and p-CN) and a carbazole-based donor CPTBF are explored for exciplex formation. The CPTBF:m-CN and CPTBF:p-CN blends show the signature red-shifted emission together with the delayed fluorescence observed in time-resolved measurement, manifesting the characteristics of thermally activated delayed fluorescence (TADF). The electroluminescence (EL) device employing CPTBF:m-CN (CPTBF:p-CN) blend as the emitting layer (EML) achieved an EQE of 5.22% (2.05%) with the EL λmax centered at 607 nm (625 nm). The exciplex excitons can be efficiently extracted by a new benzobisthiadiazole-based near-infrared (NIR) emitter DCzPBBT, where a device is configured with CPTBF:m-CN: (5 wt.%) DCzPBBT as the EML to achieve a high EQE of 5.32% and an EL λmax 758 nm. Further increase of the doping concentration to 10 wt.% of DCzPBBT exhibits a bathochromic shifted EL λmax to 772 nm with 94% spectral coverage in the NIR (>700 nm) region, while the device EQE retains at 4.06%. The superior device performance stems from the highly efficient energy transfer between the exciplex-forming host and NIR dopant together.
Original language | English |
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Article number | 2303131 |
Journal | Advanced Optical Materials |
Volume | 12 |
Issue number | 16 |
DOIs | |
Publication status | Published - 2024 Jun 6 |
Keywords
- exciplex
- intermolecular charge transfer
- near-infrared
- thermally activated delayed fluorescence
ASJC Scopus subject areas
- Electronic, Optical and Magnetic Materials
- Atomic and Molecular Physics, and Optics