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Naphthyridine-based thermally activated delayed fluorescence emitters for highly efficient blue OLEDs
摘要： Two TADF emitters 2,7-di(9H-carbazole)-1,8-naphthyridine (Cz-ND) and 2,7-di(3,6-di-tert-butyl-9H-carbazole)-1,8-naphthyridine (tBuCz-ND) were designed and synthesized. Both of the emitters showed high thermal stabilities and strong blue emissions with high photoluminescence quantum yields, and also exhibited excellent TADF properties with small ?EST values. Consequently, blue organic light-emitting diodes (OLEDs) based on Cz-ND and tBuCz-ND were fabricated, which could achieve maximum external quantum efficiencies (EQEmax) of 15.3 and 20.9%, respectively. Moreover, the devices also exhibited relatively narrow band gaps at 79 and 75 nm with the CIE coordinates of (0.15, 0.17) and (0.15, 0.22), respectively.
关键词： OLED,blue emission,carbazole,thermally activated delayed fluorescence,naphthyridine
更新于2025-09-16 10:30:52
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Recent advances in circularly polarized electroluminescence based on organic light-emitting diodes
摘要： Since the first attempt that was made to obtain direct circularly polarized (CP) light from OLEDs by Meijer et al. in 1997, considerable efforts have been devoted to the development of circularly polarized organic light-emitting diodes (CP-OLEDs), particularly in the recent years. Circularly polarized electroluminescence (CPEL) based on OLEDs has attracted increasing interest for its efficient ability to generate CP light directly and wide potential applications in 3D displays, optical data storage, and optical spintronics. In this review, we systematically summarize the recent progress in chiral emitter based OLEDs with CPEL properties including CPEL based on chiral conjugated polymers, CPEL based on chiral metal complexes, and CPEL based on chiral simple organic molecules, especially chiral thermally activated delayed fluorescence (TADF) molecules. We believe that this review will provide a promising perspective of chiral emitter based OLEDs with CPEL properties for a broad range of scientists in different disciplinary areas and attract a growing number of researchers to this fast-growing research field.
关键词： chiral simple organic molecules,circularly polarized electroluminescence,thermally activated delayed fluorescence,chiral conjugated polymers,organic light-emitting diodes,chiral metal complexes
更新于2025-09-16 10:30:52
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All-solution processed inverted QLEDs with double hole transport layers and thermal activated delay fluorescent dopant as energy transfer medium
摘要： Highly efficient, all-solution processed inverted quantum dot light-emitting diodes (QLEDs) with high performance are demonstrated by employing poly(9-vinlycarbazole) (PVK) as additional hole transport layer (HTL) and doping it with a blue thermal activated delay fluorescent (TADF) material, 4,5-bis(carbazol-9-yl)-1,2-dicyanobenzene (2CzPN). This PVK: 2CzPN composite layer not only optimizes hole injection, but also utilizes the leaked electrons to enhance device luminance by energy transfer process from 2CzPN to quantum dots (QDs). These benefits enable a 20-fold increment for the device current efficiency (from 0.523 cd/A to 11 cd/A) and a 9.9-fold improvement for the maximum luminance (from 3220 cd/m2 to 35352 cd/m2), compared with those of the standard QLED with poly[(9, 9-dioctylfluorenyl-2,7-diyl)-alt-(4,4'-(N-(4-butylphenyl) (TFB) single HTL. In comparison with the QLED with TFB/pristine PVK double HTLs, the device performance of the optimal QLED with PVK: 2CzPN additional HTL are still 40.8% and 61.7% higher in luminance and current efficiency, respectively.
关键词： Thermally activated delayed fluorescence,Quantum dot light-emitting diode,All-solution process,Energy transfer,Double hole transport layers,Inverted structure
更新于2025-09-12 10:27:22
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Facile structure-modification of xanthenone based OLED emitters exhibiting both aggregation induced emission enhancement and thermally activated delayed fluorescence
摘要： Four new donor-acceptor compounds were designed, synthesized and investigated by theoretical and experimental approaches aiming to estimate effect of the structure of a donor on the properties of potential OLED emitters. Because of the different electron-donating abilities of the nitrogen-containing heterocycles, derivatives of xanthenone containing di-tert-butyl-carbazolyl, di-tert-butyl-acridanyl, di-tert-butyl-phenothiazinyl and penoxazinyl moieties exhibited different photophysical behavior. Because of big dihedral angles between the donors and acceptor as well as because of possibility of rotation around N-C bond, the designed compounds were characterized by thermally activated delayed fluorescence and aggregation induced emission enhancement effect. Twice higher photoluminesce quantum yields reaching 38% in doped films were obtained for compounds containing di-tert-butyl-carbazolyl and di-tert-butyl-acridanyl moieties as compared to those observed for compounds with the donors containing S and O heteroatoms. Strong effect of the donor substituents on charge injection (ionization potentials were in the range of 5.67-5.96 eV) and charge-transporting properties (hole and electron mobilities were in a wide range from 6.3×10-8 to 6.3×10-4 cm2V-1s-1 at electric field of 2.5×105 V·cm-1) was detected. The differently substituted compounds were utilized as emitters in OLEDs. Higher maximum values of external quantum efficiency (up to 3.5%) were observed for OLEDs based on emitters with nitrogen containing donors relative to estimated for OLEDs based on emitters containing di-tert-butyl-phenothiazinyl and penoxazinyl moieties.
关键词： aggregation induced emission enhancement,xanthenone,Organic light-emitting diode,thermally activated delayed fluorescence
更新于2025-09-12 10:27:22
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Molecular Engineering of Thermally Activated Delayed Fluorescence Emitters with Aggregation-Induced Emission via Introducing Intramolecular Hydrogen-Bonding Interactions for Efficient Solution-Processed Nondoped OLEDs
摘要： Purely organic luminescent materials concurrently exhibiting thermally activated delayed fluorescence (TADF) and aggregation-induced emission (AIE) features are in great demand due to their high efficiency in aggregation-state toward efficient non-doped OLEDs. Herein, a class of thermally activated delayed fluorescence (TADF) emitters adopting phenyl(pyridyl)methanone as electron-accepting segment and di(tert-butyl)carbazole and 9,9-dimethyl-9,10-dihydroacridine (or phenoxazine) as electron-donating groups are designed and synthesized. The existence of intramolecular hydrogen bonding is conducive to minish the energy difference between singlet and triplet (ΔEst), suppress non-radiative decay and increase the luminescence efficiency. By using 3CPyM-DMAC as emitter, the non-doped device via solution process realize high current efficiency (CE) and external quantum efficiency (EQE) of 35.4 cd A-1 and 11.4 %, respectively, which is superior to that of CBM-DMAC with CE and EQE of 14.3 cd A-1 and 6.7 %. This work demonstrates a promising tactics to the establishment of TADF emitters with AIE features via introducing intramolecular hydrogen-bonding.
关键词： organic light-emitting diodes (OLEDs),nondoped,thermally activated delayed fluorescence (TADF),solution processed,aggregation-induced emission (AIE)
更新于2025-09-12 10:27:22
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Cyclohexane-cored dendritic host materials with high triplet energy for efficient solution-processed blue thermally activated delayed fluorescence OLEDs
摘要： Two dendritic host materials (CH-2D1 and CH-2D2) are developed by using non-conjugated cyclohexane core and two first/second generation carbazole dendrons, which show excellent solubility in organic solvents, high thermal stability and high triplet energy (ET) of 2.78–2.84 eV, making them suitable for fabrication of solution-processed blue thermally activated delayed fluorescence (TADF) organic light-emitting diodes (OLEDs). Compared to CH-2D1 with the first-generation carbazole dendron which shows low-lying highest occupied molecular orbital (HOMO) energy level of (cid:0) 5.48 eV, CH-2D2 with the second-generation carbazole dendrons exhibits higher HOMO level of (cid:0) 5.37 eV, which is more favourable for hole injection from the anode to the emissive layers. Consequently, solution-processed blue TADF OLEDs utilizing CH-2D2 as host show promising device performance with a low turn-on voltage of 3.4 V, maximum external quantum efficiency of 17.8%, (cid:0) 1, which can compare with the most efficient solution-processed blue TADF OLEDs based on small-molecule and polymer hosts. These results indicate that dendritic host materials with well-defined chemical structure and good solubility are an attractive approach–beyond the soluble small-molecule hosts and polymer hosts–for the development of efficient solution-processed TADF OLEDs.
关键词： Thermally activated delayed fluorescence,Dendritic host materials,Organic light-emitting diodes,High triplet energy
更新于2025-09-12 10:27:22
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Phthalonitrile-based bipolar host for efficient green to red phosphorescent and TADF OLEDs
摘要： A bipolar host material named 4-(9H-carbazol-9-yl)phthalonitrile (CzPN) was developed by combining carbazole and phthalonitrile as donor and acceptor units, respectively. The introduction of the phthalonitrile unit realized a relatively small energy gap of 3.00 eV as well as a deep lowest unoccupied molecular orbital level of ?2.72 eV. The characterization of carrier-only devices demonstrated the bipolar charge transporting property of CzPN. With a triplet energy of 2.70 eV, CzPN was investigated as host in green, yellow, and red phosphorescent organic light-emitting diodes (PhOLEDs) and green thermally activated delayed fluorescence (TADF) devices. A low turn-on voltage of 2.8 V was achieved by all the four diodes. Both PhOLEDs and TADF devices exhibited high external quantum efficiency values over 20% with relatively small efficiency roll-offs. These findings demonstrate that CzPN is an excellent host material for both phosphorescent and TADF emitters, and phthalonitrile is a promising unit to develop universal host materials.
关键词： Phthalonitrile,Bipolar host,Phosphorescent organic light-emitting diode,Thermally activated delayed fluorescence
更新于2025-09-12 10:27:22
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J-aggregation Enhances the Electroluminescence Performance of Sky-blue TADF Emitter in Non-doped OLEDs
摘要： A pivotal thermally activated delayed fluorescence (TADF) emitter DspiroAc-TRZ was developed, and it exhibits greatly enhanced electroluminescence performance in non-doped organic light-emitting diodes (OLEDs) owing to the concurrent manipulation of aggregation behavior and monomolecular structure. The delicate non-planar packing pattern in DspiroAc-TRZ crystal can not only lead to highly efficient solid-state luminescence, but also form loose intermolecular packing pattern, greatly decreasing the HOMOs or LUMOs overlaps in dimers and shortening triplet exciton diffusion length. In addition, the rigid donor and acceptor moieties in DspiroAc-TRZ can rigidify the molecular backbone, resulting in tiny geometry vibrational relaxation in excited state. Impressively, high photoluminescent quantum yields (PLQYs) of 78.5% and 83.7% were achieved for DspiroAc-TRZ single-crystal and non-doped film. A high external quantum efficiency (EQE) of 25.7% was achieved in non-doped sky-blue TADF-OLED, which is higher than any reported EQE values of non-doped sky-blue TADF-OLEDs so far.
关键词： molecular orientation,non-doped,thermally activated delayed fluorescence,organic electronics,organic light-emitting diodes
更新于2025-09-12 10:27:22
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Wavelength-Turnable Organic Micro-ring Laser Arrays from Thermally Activated Delayed Fluorescent Emitters
摘要： Organic solid-state lasers (OSSLs) have been paid great attention due to their ease-of-fabrication, low cost and tailor-made molecular tunability. Optical gain materials of OSSLs are currently focused on fluorescent materials, which can bring only 25% exciton utilization for future current-injection OSSLs due to spin statics under electrical excitation. While thermally active delayed fluorescent (TADF) materials can obtain a theoretical 100% internal quantum efficiency by harvesting triplet excitons. However, OSSLs based on TADF materials remain largely unexplored yet. Here, we report the first TADF-based OSSL from whispering-gallery mode micro-ring resonator arrays fabricated by a confined solution-growth method. The newly designed TADF emitter of carbozyl borondifluoride curcuminoid derivative, namely, CAZ-A, when doped into a host matrix of 4,4'-bis(N-carbazolyl)-1,10-biphenyl (CBP), reaches the highest gain-coefficient of 640 cm-1 at 4 wt%. These MRs with well-controlled sizes and uniform geometries constitute a high quality (cavity quality factor Q ~ 1300) built-in WGM resonators and exhibit outstanding multi-mode laser behaviors. By varying TADF molecule doping concentration, the laser wavelength can be continuously tuned in the red spectral range from 650 nm to 725 nm. As CBP is usually used as the host material for active layers in OLEDs, we believe that CAZ-A/CBP doping material is good candidate for future electrically driven OSSLs.
关键词： wavelength tunability,micro-ring laser arrays,whispering-gallery mode,host-guest doping,thermally activated delayed fluorescence (TADF)
更新于2025-09-12 10:27:22
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Modulation of F?rster and Dexter Interactions in Single‐Emissive‐Layer All‐Fluorescent WOLEDs for Improved Efficiency and Extended Lifetime
摘要： White organic light-emitting diodes (WOLEDs) with thermally activated delayed fluorophor sensitized fluorescence (TSF) have aroused wide attention, considering their potential for full exciton utilization without noble-metal containing phosphors. However, performances of TSF-WOLEDs with a single-emissive-layer (SEL) still suffer from low exciton utilization and insufficient blue emission for proper white balance. Here, by modulating F?rster and Dexter interactions in SEL-TSF-WOLEDs, high efficiencies, balanced white spectra, and extended lifetimes are realized simultaneously. Given the different dependencies of F?rster and Dexter interactions on intermolecular distances, sterically shielded blue thermally activated delayed fluorescence (TADF) emitters and orange conventional fluorescent dopants (CFDs) with electronically inert peripheral units are adopted to enlarge distances of electronically active chromophores, not only blocking the Dexter interaction to prevent exciton loss but also finely suppressing the F?rster one to guarantee balanced white emission with sufficient blue components. It thus provides the possibility to maximize device performances in a large range of CFD concentrations. A record high maximum external quantum efficiency/power efficiency of 19.6%/52.2 lm W?1, Commission Internationale de L’Eclairage coordinate of (0.33, 0.45), and prolonged half-lifetime of over 2300 h at an initial luminance of 1000 cd m?2 are realized simultaneously for SEL-TSF-WOLEDs, paving the way toward practical applications.
关键词： sensitizing process,thermally activated delayed fluorescence,exciton interactions,white organic light-emitting diodes,sterically inert substituents
更新于2025-09-12 10:27:22