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Carbonyl Fused Organoboron Polycyclic Aromatic Hydrocarbon for Bathochromic‐Shifted Narrowband OLED
51
Citations
47
References
2023
Year
EngineeringOrganic ElectronicsBoron/nitrogen/carbonyl Mr‐tadf EmitterOrganic ChemistryChemistryReorganization EnergyBathochromic‐shifted Narrowband OledElectronic DevicesPhosphorescence ImagingThermally Activated Delayed FluorescencePhotophysical PropertyPhotochemistryOrganic SemiconductorOrganic Charge-transfer CompoundOrganic Material ChemistryElectronic MaterialsCarbonyl‐free TczbacApplied PhysicsOptoelectronics
Abstract Polycyclic aromatic hydrocarbon (PAH) compounds are prospective materials for highly efficient narrowband organic light‐emitting diodes. Specifically, boron‐nitrogen doped PAHs exhibit multiple resonance (MR) effect toward thermally activated delayed fluorescence (TADF) and narrow full width at half‐maximum (FWHM). Currently, the molecular design strategy for bathochromic‐shifted narrowband MR‐TADF emitters is a hotspot and challenging puzzle. Herein, a carbonyl is fused in the boron‐nitrogen doped PAH for constructing a boron/nitrogen/carbonyl MR‐TADF emitter. Benefiting from the carbonyl, the developed emitter exhibits enhanced intramolecular charge transfer and decreased reorganization energy, which displays bathochromic‐shifted narrowband emission pertinently. As a consequence, the proof‐of‐concept compound TCZBAO achieves an emission peak at 522 nm and narrow FWHM of 39 nm, while the carbonyl‐free TCZBAC exhibits an emission peak at 502 nm and FWHM of 46 nm. Maximum external quantum efficiencies of 36.1 % and 32.4 % are realized for the devices based on TCZBAO and TCZBAC, respectively, indicating the guiding significance of the proposed design strategy for developing bathochromic‐shifted narrowband MR‐TADF emitters.
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