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Organic luminescent materials that exhibit thermally activated delayed fluorescence (TADF) can convert non-emissive triplet excitons into emissive singlet states through a reverse intersystem crossing (RISC) process. Therefore, they have tremendous potential for applications in organic light-emitting diodes (OLEDs). However, with the development of ultra-high definition 4K/8K display technologies, designing efficient deep-blue TADF materials to achieve the Commission Internationale de l'Éclairage (CIE) coordinates fulfilling BT.2020 remains a significant challenge. Here, an effective approach is proposed to design deep-blue TADF molecules based on hybrid long- and short-range charge-transfer by incorporation of multiple donor moieties into organoboron multiple resonance acceptors. The resulting TADF molecule exhibits deep-blue emission at 414 nm with a full width at half maximum (FWHM) of 29 nm, together with a thousand-fold increase in RISC rate. OLEDs based on the champion material achieve a record maximum external quantum efficiency (EQE) of 22.8% with CIE coordinates of (0.163, 0.046), approaching the coordinates of the BT.2020 blue standard. Moreover, TADF-assisted fluorescence devices employing the designed material as a sensitizer exhibit an exceptional EQE of 33.1%. This work thus provides a blueprint for future development of efficient deep-blue TADF emitters, representing an important milestone towards meeting the blue color gamut standard of BT.2020.
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http://dx.doi.org/10.1002/adma.202313602 | DOI Listing |
We have demonstrated a sub-nanosecond frequency-doubled potassium titanyl phosphate optical parametric oscillator with a large laser longitudinal mode spacing at 443 nm. Pumped by a 532.2 nm pulsed laser with a pulse width of 0.
View Article and Find Full Text PDFACS Appl Mater Interfaces
August 2025
State Key Laboratory of Integrated Optoelectronics, College of Electronic Science and Engineering, Jilin University, Changchun 130012, China.
With the increasing global demand for energy efficiency solutions, smart windows capable of controlling excess solar radiation and reducing electric energy usage have emerged as promising options and are undergoing substantial development. However, the use of smart windows is constrained by limitations associated with temperature regulation capabilities and damage upon accidental scratches. To overcome these obstacles, we introduce a method for creating transparent self-healing photochromic coatings by simply alternately depositing polyethylenimine (PEI)-polyoxometalate (POM) complexes and poly(acrylic acid) (PAA) on glass substrates.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Soochow University, Suzhou, 215123, China.
The development of blue perovskite light-emitting diodes (PeLEDs) is critical for advancing next-generation display technologies. However, the fabrication of high-quality mixed-halide blue perovskites remains challenging due to their intrinsic vulnerability to high defect densities, ion migration, and inefficient charge transport. To address this, we introduce a rapid in situ interface reaction at the buried interface between the perovskite layer and the underlying poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) film.
View Article and Find Full Text PDFAdv Mater
August 2025
Strait Institute of Flexible Electronics (SIFE, Future Technologies), Fujian Key Laboratory of Flexible Electronics, Fujian Normal University and Strait Laboratory of Flexible Electronics (SLoFE), Fuzhou, Fujian, 350117, China.
Achieving high phosphorescence efficiency and photo-activated ultralong organic phosphorescence (UOP) based on the same molecule remains a formidable challenge. Here, a concise strategy is proposed to obtain highly efficient and photo-activated RTP by doping aromatic heterocyclic derivatives into different polymers. Aromatic heterocyclic derivatives are doped into PAM, PVA, or PAA polymers to produce high phosphorescence efficiency.
View Article and Find Full Text PDFJ Phys Chem Lett
August 2025
Advanced Photofunctional Materials Laboratory, Department of Chemistry, Shiv Nadar Institution of Eminence, Delhi NCR, NH-91, Tehsil Dadri, Gautam Buddha Nagar 201314, Uttar Pradesh, India.
Achieving thermally activated delayed fluorescence (TADF) from covalently assembled multiple donor-acceptor (D-A) units is challenging due to complex design issues. Here, we use a cyclic multiple donor-acceptor (CPCQ) design approach that includes four nonconjugated TADF active D-A units. Spectroscopic analysis revealed that CPCQ emits deep blue TADF (430 nm) with (a) a high photoluminescence quantum yield (PLQY, 78-80%), (b) a high reverse intersystem crossing rate (k = 2.
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