Intramolecular Cyclization: A Convenient Strategy to Realize Efficient BT.2020 Blue Multi-Resonance Emitter for Organic Light-Emitting Diodes

Rationally tuning the emission position and narrowing the full width at half-maximum (FWHM) of an emitter is of great importance for many applications. By synergistically improving rigidity, strengthening the resonant strength, inhibiting molecular bending and rocking, and destabilizing the HOMO energy level, a deep-blue emitter (CZ2CO) with a peak wavelength of 440 nm and an ultranarrow spectral FWHM of 16 nm (0.10 eV) was developed via intramolecular cyclization in a carbonyl/N resonant core (QAO). The dominant υ_0-0 transition character of CZ2CO gives a Commission Internationale de I’Éclairage coordinates (CIE) of (0.144, 0.042), nicely complying with the BT.2020 standard. Moreover, a hyper-fluorescent device based on CZ2CO shows a high maximum external quantum efficiency (EQE_max) of 25.6 % and maintains an EQE of 22.4 % at a practical brightness of 1000 cd m⁻².     

Doubly Boron-Doped TADF Emitters Decorated with ortho-Donor Groups for Highly Efficient Green to Red OLEDs

Doubly boron-doped thermally activated delayed fluorescence (TADF) emitters based on a 9,10-diboraanthracene (DBA) acceptor decorated with ortho-donor groups (Cz2oDBA, 2 ; BuCz2oDBA, 3 ; DMAC2oDBA, 4 ) are prepared to realize high-efficiency green-to-red organic light-emitting diodes (OLEDs). X-ray diffraction analyses of 2 and 4 reveal the symmetrical and highly twisted ortho-donor–acceptor–donor (D-A-D) structure of the emitters. The twisted conformation leads to a very small energy splitting (ΔE_ST <0.08 eV) between the excited singlet and triplet states that gives rise to strong TADF, as supported by theoretical studies. Depending on the strength of the donor moieties, the emission color is fine-tuned in the visible region from green ( 2 ) to yellow ( 3 ) to red ( 4 ). Carbazole-containing 2 and 3 exhibit high photoluminescence quantum yields (PLQYs) approaching 100 %, whereas DMAC-substituted 4 is moderately emissive (PLQY=44 %) in a doped host film. Highly efficient green-to-red TADF-OLEDs are realized with the proposed ortho-D-A-D compounds as emitters. The green and yellow OLEDs incorporating Cz2oDBA ( 2 ) and BuCz2oDBA ( 3 ) emitters exhibit high external quantum efficiencies (EQEs) of 26.6 % and 21.6 %, respectively. In particular, the green device shows an excellent power efficiency above 100 lm W⁻¹. A red OLED fabricated with a DMAC2oDBA ( 4 ) emitter exhibits a maximum EQE of 10.1 % with an electroluminescence peak at 615 nm.     

Strongly Luminescent Tungsten Emitters with Emission Quantum Yields of up to 84 %: TADF and High‐Efficiency Molecular Tungsten OLEDs

Metal‐TADF (thermally activated delayed fluorescence) emitters hold promise in the development of next generation light‐emitting materials for display and lighting applications, examples of which are, however, largely confined to Cu^I and recently Au^I, Ag^I, and Au^III emitters. Herein is described the design strategy for an unprecedented type of metal‐TADF emitter based on inexpensive tungsten metal chelated with Schiff base ligand that exhibit high emission quantum yields of up to 56 % in solutions and 84 % in thin‐film (5 wt % in 1,3‐bis(N‐carbazolyl)benzene, mCP) at room temperature. Femtosecond time‐resolved emission (fs‐TRE) spectroscopy and DFT calculations were undertaken to decipher the TADF properties. Solution‐processed OLEDs fabricated with the W‐TADF emitter demonstrated external quantum efficiency (EQE) and luminance of up to 15.6 % and 16890 cd m^?2, respectively.