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Weak emissive D-O-A organic phosphor: Exceptional matrix-free sensitization in MR-TADF OLEDs

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    1. A weakly emissive D–O–A organic phosphor is developed to act as an efficient sensitizer for MR–TADF emitters.

      High-performance narrowband electroluminescence is achieved ranging from sky blue to red.

      The exceptional results break a habitual thinking that the best sensitizer should be the best emitter.

  • D-O-A organic phosphors showing strong aggregation-induced room-temperature phosphorescence (RTP) have been successfully demonstrated as the ideal matrix-free sensitizers for MR-TADF OLEDs. However, weak emissive ones still remain unexplored according to a habitual thinking that the best sensitizer should be the best emitter. Herein, a poor RTP emitter named RTP-D3 is newly developed based on carbazole as the donor, triazine as the acceptor and oxygen as the bridge. In spite of the extremely low photoluminescence quantum yield, RTP-D3 can sensitize the terminal MR-TADF molecules effectively and universally because of favored π-π and C-H∙∙∙π intermolecular interactions among triazine moieties and thus a balanced charge transport. Consequently, high performance sky-blue, green, yellow and red narrowband electroluminescence is realized together with a state-of-art external quantum efficiency of 22.2% (49.2 cd/A, 55.2 lm/W), 31.5% (105.1 cd/A, 113.9 lm/W), 32.9% (112.4 cd/A, 133.3 lm/W) and 29.7% (55.4 cd/A, 66.9 lm/W) as well as Commission Internationale de l’Eclairage (CIE) coordinates of (0.12, 0.48), (0.26, 0.70), (0.45, 0.54) and (0.61, 0.39), respectively. The exceptional results break a conventional blind spot about RTP sensitizer, highlighting that the less emissive D-O-A organic phosphors are also suitable for the best matrix-free sensitization in MR-TADF OLEDs.
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  • [1] Hatakeyama T., Shiren K., Nakajima K., et al. (2016). Ultrapure blue thermally activated delayed fluorescence molecules: Efficient HOMO-LUMO separation by the multiple resonance effect. Adv. Mater. 28:2777−2781. DOI:10.1002/adma.201505491

    View in Article CrossRef Google Scholar

    [2] Fan X., Hao X., Huang F., et al. (2023). RGB thermally activated delayed fluorescence emitters for organic light-emitting diodes toward realizing the BT.2020 standard. Adv. Sci. 10:2303504. DOI:10.1002/advs.202303504

    View in Article Google Scholar

    [3] Suresh S. M., Hall D., Beljonne D., et al. (2020). Multiresonant thermally activated delayed fluorescence emitters based on heteroatom-doped nanographenes: Recent advances and prospects for organic light-emitting diodes. Adv. Funct. Mater. 30:1908677. DOI:10.1002/adfm.201908677

    View in Article CrossRef Google Scholar

    [4] Kothavale S. S. and Lee J. Y. (2020). Three- and four-coordinate, boron-based, thermally activated delayed fluorescent emitters. Adv. Opt. Mater. 8:2000922. DOI:10.1002/adom.202000922

    View in Article CrossRef Google Scholar

    [5] Kim H. J. and Yasuda T. (2022). Narrowband emissive thermally activated delayed fluorescence materials. Adv. Opt. Mater. 10:2201714. DOI:10.1002/adom.202201714

    View in Article CrossRef Google Scholar

    [6] Jiang H., Jin J. and Wong W.-Y. (2023). High-performance multi-resonance thermally activated delayed fluorescence emitters for narrowband organic light-emitting diodes. Adv. Funct. Mater. 33:2306880. DOI:10.1002/adfm.202306880

    View in Article CrossRef Google Scholar

    [7] Xu Y., Wang Q., Cai X., et al. (2023). Frontier molecular orbital engineering: Constructing highly efficient narrowband organic electroluminescent materials. Angew. Chem. Int. Ed. 62:e202312451. DOI:10.1002/anie.202312451

    View in Article CrossRef Google Scholar

    [8] Kondo Y., Yoshiura K., Kitera S., et al. (2019). Narrowband deep-blue organic light-emitting diode featuring an organoboron-based emitter. Nat. Photon. 13:678−682. DOI:10.1038/s41566-019-0476-5

    View in Article CrossRef Google Scholar

    [9] Suresh S. M., Duda E., Hall D., et al. (2020). A deep blue B,N-doped heptacene emitter that shows both thermally activated delayed fluorescence and delayed fluorescence by triplet-triplet annihilation. J. Am. Chem. Soc. 142:6588−6599. DOI:10.1021/jacs.9b13704

    View in Article CrossRef Google Scholar

    [10] Xu Y., Li C., Li Z., et al. (2020). Constructing charge-transfer excited states based on frontier molecular orbital engineering: Narrowband green electroluminescence with high color purity and efficiency. Angew. Chem. Int. Ed. 59:17442−17446. DOI:10.1002/anie.202007210

    View in Article CrossRef Google Scholar

    [11] Zhang Y., Zhang D., Huang T., et al. (2021). Multi-resonance deep-red emitters with shallow potential-energy surfaces to surpass energy-gap law. Angew. Chem. Int. Ed. 60:20498−20503. DOI:10.1002/anie.202107848

    View in Article CrossRef Google Scholar

    [12] Park I. S., Min H. and Yasuda T. (2022). Ultrafast triplet-singlet exciton interconversion in narrowband blue organoboron emitters doped with heavy chalcogens. Angew. Chem. Int. Ed. 61:e202205684. DOI:10.1002/anie.202205684

    View in Article CrossRef Google Scholar

    [13] Hu Y. X., Miao J., Hua T., et al. (2022). Efficient selenium-integrated TADF OLEDs with reduced roll-off. Nat. Photon. 16:803−810. DOI:10.1038/s41566-022-01083-y

    View in Article CrossRef Google Scholar

    [14] Fan X.-C., Wang K., Shi Y.-Z., et al. (2023). Ultrapure green organic light-emitting diodes based on highly distorted fused π-conjugated molecular design. Nat. Photon. 17:280−285. DOI:10.1038/s41566-022-01106-8

    View in Article CrossRef Google Scholar

    [15] Wan D., Zhou J., Meng G., et al. (2024). Peripheral carbazole units-decorated MR emitter containing B−N covalent bond for highly efficient green OLEDs with low roll-off. J. Semicond. 45:082402. DOI:10.1088/1674-4926/24040008

    View in Article CrossRef Google Scholar

    [16] Wan D., Zhou J., Yang Y., et al. (2024). Peripheral substitution engineering of MR-TADF emitters embedded with B-N covalent bond towards efficient BT.2020 blue electroluminescence. Adv. Mater. 36:2409706. DOI:10.1002/adma.202409706

    View in Article Google Scholar

    [17] Zhang Y., Wei J., Zhang D., et al. (2022). Sterically wrapped multiple resonance fluorophors for suppression of concentration quenching and spectrum broadening. Angew. Chem. Int. Ed. 61:e202113206. DOI:10.1002/anie.202113206

    View in Article CrossRef Google Scholar

    [18] Zhang D., Song X., Gillett A. J., et al. (2020). Efficient and stable deep-blue fluorescent organic light-emitting diodes employing a sensitizer with fast triplet upconversion. Adv. Mater. 32:1908355. DOI:10.1002/adma.201908355

    View in Article CrossRef Google Scholar

    [19] Jeon S. O., Lee K. H., Kim J. S., et al. (2021). High-efficiency, long-lifetime deep-blue organic light-emitting diodes. Nat. Photon. 15:208−215. DOI:10.1038/s41566-021-00763-5

    View in Article CrossRef Google Scholar

    [20] Chan C.-Y., Tanaka M., Lee Y.-T., et al. (2021). Stable pure-blue hyperfluorescence organic light-emitting diodes with high-efficiency and narrow emission. Nat. Photon. 15:203−207. DOI:10.1038/s41566-020-00745-z

    View in Article CrossRef Google Scholar

    [21] Adachi C. (2014). Third-generation organic electroluminescence materials. Jpn. J. Appl. Phys. 53:060101. DOI:10.7567/JJAP.53.060101

    View in Article CrossRef Google Scholar

    [22] Liu Y., Li C., Ren Z., et al. (2018). All-organic thermally activated delayed fluorescence materials for organic light-emitting diodes. Nat. Rev. Mater. 3:18020. DOI:10.1038/natrevmats.2018.20

    View in Article CrossRef Google Scholar

    [23] Cai M., Zhang D. and Duan L. (2019). High performance thermally activated delayed fluorescence sensitized organic light-emitting diodes. Chem. Rec. 19:1611−1623. DOI:10.1002/tcr.201800148

    View in Article CrossRef Google Scholar

    [24] Chen J., Liu H., Guo J., et al. (2022). Robust luminescent molecules with high-level reverse intersystem crossing for efficient near ultraviolet organic light-emitting diodes. Angew. Chem. Int. Ed. 61:e202116810. DOI:10.1002/anie.202116810

    View in Article CrossRef Google Scholar

    [25] Cho H.-H., Congrave D. G., Gillett A. J., et al. (2024). Suppression of Dexter transfer by covalent encapsulation for efficient matrix-free narrowband deep blue hyperfluorescent OLEDs. Nat. Mater. 23:519−526. DOI:10.1038/s41563-024-01812-4

    View in Article CrossRef Google Scholar

    [26] Zhang D., Duan L., Li C., et al. (2014). High-efficiency fluorescent organic light-emitting devices using sensitizing hosts with a small singlet-triplet exchange energy. Adv. Mater. 26:5050−5055. DOI:10.1002/adma.201401476

    View in Article CrossRef Google Scholar

    [27] Cho H.-H., Romanov A. S., Bochmann M., et al. (2021). Matrix-free hyperfluorescent organic light-emitting diodes based on carbene-metal-amides. Adv. Opt. Mater. 9:2001965. DOI:10.1002/adom.202001965

    View in Article CrossRef Google Scholar

    [28] Zhang Q., Tsang D., Kuwabara H., et al. (2015). Nearly 100% internal quantum efficiency in undoped electroluminescent devices employing pure organic emitters. Adv. Mater. 27:2096−2100. DOI:10.1002/adma.201405474

    View in Article CrossRef Google Scholar

    [29] Li X., Yan L., Liu S., et al. (2023). Polymerized thermally activated delayed-fluorescence small molecules: Long-axis polymerization leads to a nearly concentration-independent luminescence. Angew. Chem. Int. Ed. 62:e202300529. DOI:10.1002/anie.202300529

    View in Article CrossRef Google Scholar

    [30] Su N., Chen B. and Ding J. (2024). Two birds with one stone: polymerized thermally activated delayed fluorescence small molecules. Chem. Eur. J. 30:e202304095. DOI:10.1002/chem.202304095

    View in Article CrossRef Google Scholar

    [31] Zhao W., He Z. and Tang B. Z. (2020). Room-temperature phosphorescence from organic aggregates. Nat. Rev. Mater. 5:869−885. DOI:10.1038/s41578-020-0223-z

    View in Article CrossRef Google Scholar

    [32] Liu X., Yang L., Li X., et al. (2021). An electroactive pure organic room-temperature phosphorescence polymer based on a donor-oxygen-acceptor geometry. Angew. Chem. Int. Ed. 60:2455−2463. DOI:10.1002/anie.202011957

    View in Article CrossRef Google Scholar

    [33] Xu L., Mo Y., Su N., et al. (2023). D-O-A based organic phosphors for both aggregation-induced electrophosphorescence and host-free sensitization. Nat. Commun. 14:1678. DOI:10.1038/s41467-023-37414-y

    View in Article CrossRef Google Scholar

    [34] Stavrou K., Franca L. G., Danos A., et al. (2024). Key requirements for ultraefficient sensitization in hyperfluorescence organic light-emitting diodes. Nat. Photon. 18:554−561. DOI:10.1038/s41566-024-01395-1

    View in Article CrossRef Google Scholar

    [35] El-Sayed M. A. (1963). Spin-orbit coupling and the radiationless processes in nitrogen heterocyclics. J. Chem. Phys. 38:2834−2838. DOI:10.1063/1.1733610

    View in Article CrossRef Google Scholar

    [36] Lee D. R., Lee K. H., Shao W., et al. (2020). Heavy atom effect of selenium for metal-free phosphorescent light-emitting diodes. Chem. Mater. 32:2583−2592. DOI:10.1021/acs.chemmater.0c00078

    View in Article CrossRef Google Scholar

    [37] Baldo M. A., O’Brien D. F., Thompson M. E., et al. (1999). Excitonic singlet-triplet ratio in a semiconducting organic thin film. Phys. Rev. B. 60:14422. DOI:10.1103/PhysRevB.60.14422

    View in Article CrossRef Google Scholar

    [38] Liu J., Zhu Y., Tsuboi T., et al. (2022). Toward a BT.2020 green emitter through a combined multiple resonance effect and multi-lock strategy. Nat. Commun. 13:4876. DOI:10.1038/s41467-022-32607-3

    View in Article Google Scholar

    [39] Chen Y., Zhang Y., Huang T., et al. (2022). Highly efficient and nearly roll-off–free electrofluorescent devices via multiple sensitizations. Sci. Adv. 8:eabp9203. DOI:10.1126/sciadv.abp9203

    View in Article CrossRef Google Scholar

    [40] Zou Y., Hu J., Yu M., et al. (2022). High-performance narrowband pure-red OLEDs with external quantum efficiencies up to 36.1% and ultralow efficiency roll-off. Adv. Mater. 34:2201442. DOI:10.1002/adma.202201442

    View in Article Google Scholar

    [41] Xu Y., Cheng Z., Li Z., et al. (2020). Molecular-structure and device-configuration optimizations toward highly efficient green electroluminescence with narrowband emission and high color purity. Adv. Opt. Mater. 8:1902142. DOI:10.1002/adom.201902142

    View in Article CrossRef Google Scholar

    [42] Qi Y., Ning W., Zou Y., et al. (2021). Peripheral decoration of multi-resonance molecules as a versatile approach for simultaneous long-wavelength and narrowband emission. Adv. Funct. Mater. 31:2102017. DOI:10.1002/adfm.202102017

    View in Article CrossRef Google Scholar

    [43] Blom P. W. M., de Jong M. J. M. and Vleggaar J. J. M. (1996). Electron and hole transport in poly(p-phenylene vinylene) devices. Appl. Phys. Lett. 68:3308−3310. DOI:10.1063/1.116583

    View in Article CrossRef Google Scholar

    [44] Chen C.-H., Lin S.-C., Lin B.-Y., et al. (2022). New bipolar host materials for high power efficiency green thermally activated delayed fluorescence OLEDs. Chem. Eng. J. 442:136292. DOI:10.1016/j.cej.2022.136292

    View in Article CrossRef Google Scholar

  • Cite this article:

    Xu L., Xiao S., Yang Y., et al. (2026). Weak emissive D-O-A organic phosphor: Exceptional matrix-free sensitization in MR-TADF OLEDs. The Innovation Materials 4:100210. https://doi.org/10.59717/j.xinn-mater.2026.100210
    Xu L., Xiao S., Yang Y., et al. (2026). Weak emissive D-O-A organic phosphor: Exceptional matrix-free sensitization in MR-TADF OLEDs. The Innovation Materials 4:100210. https://doi.org/10.59717/j.xinn-mater.2026.100210

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