Deep blue high-efficiency solution-processed triplet-triplet annihilation organic light-emitting diodes using bis(8-carbazol-N-yl)fluorene- and benzonitrile-modified anthracene/chrysene fluorescent emitters DOI

Suwapat Kongsabay,

Kasin Rueantong,

Thidarat Loythaworn

et al.

Journal of Photochemistry and Photobiology A Chemistry, Journal Year: 2024, Volume and Issue: unknown, P. 116046 - 116046

Published: Sept. 1, 2024

Language: Английский

Recent Advances in Narrow Emission Bandwidth Materials for Application in Organic Light‐Emitting Diodes DOI Open Access
Jia-Min Kang, Dong Jin Shin, Jun Yeob Lee

et al.

Advanced Optical Materials, Journal Year: 2025, Volume and Issue: unknown

Published: Feb. 21, 2025

Abstract The preparation of narrow emission bandwidth materials is crucial for the development advanced organic light‐emitting diodes (OLEDs). In this review article, state‐of‐the‐art methodologies used emitters with high color purity are summarized, and favorable design strategies rationally organized. Currently OLEDs have some issues, such as device stabilization that must be resolved, should also considered. Given recent exponential growth in number types narrowband emissive organometallic complexes exhibiting multiple‐resonance thermally activated delayed fluorescence metal‐to‐ligand charge transfer characteristics, there an urgent need to establish key technology descriptors purity. review, developments boron, fused indolocarbazole, carbonyl, phosphine oxide, exhibit spectra described, future directions advance performance devices suggested.

Language: Английский

Citations

3

Peripheral Substitution Engineering of MR‐TADF Emitters Embedded With B‒N Covalent Bond Towards Efficient BT.2020 Blue Electroluminescence DOI

Danrui Wan,

Jianping Zhou, Ying Yang

et al.

Advanced Materials, Journal Year: 2024, Volume and Issue: unknown

Published: Oct. 15, 2024

Compared with the classical boron/nitrogen (B/N) doped ones, multiple-resonance thermally activated delayed fluorescence (MR-TADF) emitters embedded B-N covalent bond behave a significantly blue-shifted narrowband TADF, and thus show greater potential in ultrapure blue organic light-emitting diodes (OLEDs). As proof of concept, herein peripheral substitution engineering is demonstrated based on such B‒N parent core. The simple approach found to ensure easy synthesis via one-pot lithium-free borylation-annulation, manipulate excited states through different electronic coupling between core substituent, introduce steric hindrance minimize unwanted spectral broadening. Impressively, OLEDs are realized give high external quantum efficiency 20.3% together Commission Internationale de l'Éclairage coordinates (0.152, 0.046). performance well competent those B/N MR-TADF emitters, clearly highlighting that framework novel promising paradigm towards efficient BT.2020 standard.

Language: Английский

Citations

12

Bifunctional Group Modulation Strategy Enables MR‐TADF Electroluminescence Toward BT.2020 Green Light Standard DOI Open Access
Lin Wu,

Ziru Xin,

Denghui Liu

et al.

Advanced Materials, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 23, 2025

Abstract Herein, a parallel “bifunctional group” modulation method is proposed to achieve controlled of the emission wavelength and full‐width at half‐maximum (FWHM) values. As result, three proof‐of‐concept emitters, namely DBNDS‐TPh, DBNDS‐DFPh, DBNDS‐CNPh, are designed synthesized, with first functional dibenzo[ b,d ]thiophene unit concurrently reducing bandgap elevate their triplet state energy. A second group 1 , ′: 3 ′, ″‐ triphenyl electron acceptors 1,3‐difluorobenzene benzonitrile respectively, deepen HOMO LUMO levels. Accordingly, CIE coordinates DBNDS‐CNPh (0.13, 0.77), (0.14, 0.76) in dilute toluene solution. This marks instance achieving y value 0.77 solutions. Significantly, non‐sensitized pure‐green OLEDs based on DBNDS‐TPh DBNDS‐DFPh demonstrate peak EQE 35.0% 34.5%, corresponding (0.18, 0.75), (0.17, doping concentration wt.%, representing green OLED reaching 0.76 bottom‐emitting device structure as reported literature.

Language: Английский

Citations

2

High Color Purity Deep‐Blue Multi‐Resonance TADF Material with Narrowband Emission Toward BT.2020 Standard DOI Open Access
Hanrui Su, Yaxiong Wang,

Kaiyuan Di

et al.

Advanced Functional Materials, Journal Year: 2024, Volume and Issue: unknown

Published: Dec. 17, 2024

Abstract Due to higher exciton energy, the deep‐blue organic light‐emitting diodes (OLEDs) are most challenging among trichromatic emitters. In this work, three novel blue emitters with multi‐resonance (MR) effects reported based on N , ,5,9‐tetraphenyl‐5,9‐dihydro‐5,9‐diaza‐13b‐boranaphtho[3,2,1‐ de ]anthracen‐7‐amine (PAB) skeleton, incorporating fluorine and methyl groups. Compound 2FPAB MePAB exhibit ultra‐pure emission peaks at 436 448 nm respectively. The device achieves a maximum external quantum efficiency of 19.8% an ultralow CIEy value 0.046 full‐width‐at‐half‐maximum (FWHM) 29 in bottom emitting device. Additionally, peripheral cladding atoms extends conjugation framework slightly enhances electron acceptance character boron atom ortho‐position. This leads redshift spectrum enhanced photoluminescence yield (PLQY) up 93% for MePABF. Furthermore, potential application as sensitizer MePABF is examined by fabricating TADF‐sensitized‐TADF (TST) results show significantly reduced roll‐off improved performance, (EQE max ) 25.1% FWHM nm.

Language: Английский

Citations

3

High‐Performance Red OLEDs Enabled by an Organoboron‐Nitrogen‐Carbonyl‐Hybridized Multiresonant Emitter DOI Open Access

Ying‐Chun Cheng,

Rajat Walia,

Tuotuo Zhang

et al.

Advanced Optical Materials, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 17, 2025

Abstract Organoboron‐nitrogen‐carbonyl‐hybridized ( h ‐BNCO) frameworks are emerging templates for developing high‐performance multiresonant (MR) emitters, but their potentials have not been fully explored. In this study, a novel red MR emitter, namely, ‐BNCO‐3, is developed by decorating two diphenylamine moieties onto ‐BNCO skeleton ‐BNCO‐2). Compared with the green backbone, ‐BNCO‐3 achieves substantial emission redshift of 76 nm while retaining narrow full width at half maximum (FWHM) 45 (0.16 eV) in toluene. Moreover, common advantages integrating carbonyl group B/N‐based systems, e.g., significant nπ * contribution triplet manifolds, obvious ‐BNCO‐3. Thus, obtained fast reverse intersystem crossing rate k RISC ) over 10 5 s −1 . The optimized non‐sensitized organic light‐emitting diode (OLED) based on achieved an external quantum efficiency (EQE) 26.4%. further employing phosphor as sensitizer, ‐BNCO‐3‐based OLED can reach impressive EQE 38.0%, which among best results MR‐OLEDs. This work demonstrates effectiveness into organoboron‐nitrogen‐based peripheral decorations enhancing , offering new insights emitters systems.

Language: Английский

Citations

0

Multi-Resonance Skeleton Connected by Rigid B- and N-embedded Dioxygen-bridged Units: Investigating Structure–Property Relationships DOI
Zhen Jiang, Qiyin Chen, Chao Shi

et al.

Dyes and Pigments, Journal Year: 2025, Volume and Issue: unknown, P. 112681 - 112681

Published: Jan. 1, 2025

Language: Английский

Citations

0

Molecular Engineering Accelerating Reverse Intersystem Crossing Endowed by Confining Donor to Ensure Low Efficiency Roll-Off OLEDs DOI
Feng Wang, Zhao Song,

Yali Peng

et al.

ACS Materials Letters, Journal Year: 2025, Volume and Issue: unknown, P. 787 - 795

Published: Jan. 30, 2025

Language: Английский

Citations

0

Boraporphyrins: Unlocking Global Aromaticity in Organoboron Macrocycles DOI

Lukas Swoboda,

Jonas Klopf,

Manuel Buckel

et al.

Journal of the American Chemical Society, Journal Year: 2025, Volume and Issue: unknown

Published: March 7, 2025

We report the synthesis of 5-bora-21,22-dioxaporphyrin 5 and its main-group d-block metal complexes 6 7, respectively. These macrocyclic boranes constitute first examples neutral porphyrins with boron in a meso-position that exhibit global aromaticity. This is evidenced by spectroscopic structural features as well calculated nucleus independent chemical shifts (NICS) anisotropic induced current densities (ACID). The boraporphyrins absorb light strongly red spectral region (Q bands) show enhanced fluorescence higher quantum yields (5: 29%) compared to conventional porphyrins. DFT calculations reveal incorporation borane moiety has distinct impact on frontier orbital energies, thus leading altered electrochemical optical properties.

Language: Английский

Citations

0

Enhancing Electroluminescence Performance of Ultra-Deep-Blue Through-Space Charge Transfer Emitters with CIEy ≈ 0.05 Via Methyl-modification DOI Creative Commons
Quanwei Li,

Haisong Zhao,

Jinyang Zhao

et al.

Chemical Science, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 1, 2025

A methyl-modification strategy is proposed to enhance the ICT and RISC processes of ultra-deep-blue through-space charge transfer emitters. The prepared emitter 3MeCz-BO achieves a high EQE max 10.1% with CIE coordinates (0.151, 0.051).

Language: Английский

Citations

0

High‐Temperature‐Induced Fused Polycyclic Aromatic Multiple Resonance Emitters Exhibiting Narrowband and Pronounced Red‐Shifted Emission DOI Open Access

Xilin Mu,

Lin Wu, Zhizhi Li

et al.

Small, Journal Year: 2025, Volume and Issue: unknown

Published: March 10, 2025

Synthetic methodology is a fundamental framework for preparing functional materials, significantly advancing their development. Herein, novel 6π electrocyclization reaction unexpectedly discovered that promotes further ring closure in materials derived from multi-resonance thermally activated delayed fluorescence (MR-TADF) compounds, known narrow emission. By simply raising the temperature, this process red-shifts emission peak of target material while effectively narrowing its emissive width and greatly enhancing optoelectronic performance. Utilizing method, newly synthesized MR-TADF substrate GCz-4B2 successfully converted into compound GCz-4B1. Compared to GCz-4B2, GCz-4B1 exhibited redshift 26 nm concurrently achieving significant reduction full at half-maximum (FWHM) value corresponding shoulder intensity. Notably, photoluminescence quantum yield (PLQY) reached 95.1%, compared only 85.6% GCz-4B2. This enhancement can be attributed increased rigidity reaction, which reduced unfavorable vibrational relaxation processes improved PLQY values. Furthermore, OLEDs based on attained maximum external efficiency (EQEmax) 28.0%, with small FWHM 19.4 nm, surpassing devices

Language: Английский

Citations

0