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Selenium-containing multiple resonance thermally activated delayed fluorescence (MR-TADF) materials with ultra-fast reverse intersystem crossing (RISC) have emerged as a promising solution for mitigating efficiency roll-off in organic light-emitting diodes (OLEDs). In this work, we introduce DBSeBN, the first MR-TADF emitter incorporating a rigid five-membered dibenzoselenophene unit. This design simultaneously achieves a narrow full width at half maximum of 23 nm across a wide range of doping concentrations in films, along with an ultra-fast RISC rate of 1.1 × 10 s, which is two orders higher than that of its sulfur-containing counterpart, DBTBN, due to the enhanced spin-orbit coupling via the heavy atom effect of selenium. As an OLED emitter, DBSeBN demonstrates exceptional performance, achieving a maximum external quantum efficiency of 31.6% and retaining 23.3% at 1000 cd m, surpassing DBTBN in suppressing efficiency roll-off. Its remarkably fast RISC and insensitivity to doping concentration enable unprecedented versatility in advanced OLED architectures. As a sensitizer in sensitized green-fluorescent OLEDs, it surpasses Ir-based complex sensitizers in reducing efficiency roll-off. As a blue emitter in bi-color white OLEDs, it effectively harnesses high-energy triplet excitons to minimize efficiency roll-off. DBSeBN thus expands the scope of MR-TADF materials across various kinds of OLED applications while suppressing efficiency roll-off.
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http://dx.doi.org/10.1002/anie.202507626 | DOI Listing |
Nat Commun
September 2025
Key Lab of Organic Optoelectronics and Molecular Engineering of Ministry of Education, Department of Chemistry, Tsinghua University, Beijing, China.
Perovskite quantum dot light-emitting diodes have rapidly achieved high external quantum efficiencies of over 25%; however, hindered by limited operating stability originating from surface defects or ion migration in quantum dots. Here, we design a lattice-matched anchoring molecule, tris(4-methoxyphenyl)phosphine oxide (TMeOPPO-p), to anchor the multi-site defects and stabilise the lattice. The target quantum dots exhibit high exciton recombination features with near-unity photoluminescence quantum yields (97%), and the as-fabricated quantum dot light-emitting diodes present a maximum external quantum efficiency of up to 27% at 693 nm, a low efficiency roll-off (over 20% at a current density of 100 mA cm for the typical device) and an operating half-life of over 23,000 h.
View Article and Find Full Text PDFChem Sci
August 2025
Key Laboratory of Theoretical and Computational Photochemistry of the Chinese Ministry of Education, College of Chemistry, Beijing Normal University Beijing 100875 P. R. China
As a class of functional materials used in organic light-emitting diodes (OLEDs), sensitizers play a crucial role in the improvement of device efficiency, color purity, and stability. In recent years, thermally activated delayed fluorescence (TADF) sensitizers have attracted much attention mainly because of their high exciton utilization efficiency by converting quenched triplet excitons into singlet excitons. Despite the experimental success of sensitization strategies in enhancing OLED performance, the lack of theoretical models for sensitizers continues to hinder further development.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Shenzhen Key Laboratory of New Information Display and Storage Materials, College of Materials Science and Engineering, Shenzhen University, Shenzhen, 518060, P.R. China.
The organic light-emitting diode (OLED) performance of multi-resonance thermally activated delayed fluorescence (MR-TADF) emitters is fundamentally constrained by their slow reverse intersystem crossing (RISC) and pronounced aggregation-caused quenching (ACQ). Herein, through regioselective borylation, we design and synthesize a series of blue MR-TADF emitters. The regioisomerization-directed twist configuration synergistically enhances RISC while suppressing ACQ, without compromising spectral purity.
View Article and Find Full Text PDFChem Commun (Camb)
August 2025
Shenzhen Key Laboratory of New Information Display and Storage Materials, College of Materials Science and Engineering, Shenzhen University, Shenzhen 518060, China.
A simple-structure, pure-organic TADF sensitizer, namely, CFBOPXZ, targeting red hyperfluorescence was designed and synthesized. CFBOPXZ exhibits simultaneous high PLQY, rapid radiative decay and reverse intersystem crossing rates, enabling stable and narrowband red hyperfluorescent OLEDs with an external quantum efficiency of 40% and minimal efficiency roll-off.
View Article and Find Full Text PDFAdv Mater
August 2025
Ji Hua Laboratory, No.28 Island Ring South Road, Foshan, 528200, P. R. China.
Developing thermally activated delayed fluorescence (TADF) materials with excellent chiroptical and photophysical properties is crucial for advancing optoelectronic applications. Herein, a chiral space conjugation strategy incorporating a typical [2.2]paracyclophane unit is proposed to construct a highly efficient chiral multi-resonant (MR) TADF emitter, R(S)-PCP-DBNO.
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