journal article·2021-11

Confining isolated chromophores for highly efficient blue phosphorescence

Wenpeng Ye, Huili Ma, Huifang Shi, He Wang, Anqi Lv, Lifang Bian, Meng Zhang, Chaoqun Ma, Kun Ling, Mingxing Gu, Yufeng Mao, Xiaokang Yao, Chaofeng Gao, Kang Shen, Wenyong Jia, Jiahuan Zhi, Suzhi Cai, Zhicheng Song, Jingjie Li, Yanyun Zhang, Song Lu, Kun Liu, Chaomin Dong, Qian Wang, Yudong Zhou, Wei Yao, Yujian Zhang, Hongmei Zhang, Zaiyong Zhang, Xiaochun Hang, Zhongfu An, Xiaogang Liu, Wei Huang

Nature Materials· Volume 20· Issue 11
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Abstract

High-efficiency blue phosphorescence emission is essential for organic optoelectronic applications. However, synthesizing heavy-atom-free organic systems having high triplet energy levels and suppressed non-radiative transitions-key requirements for efficient blue phosphorescence-has proved difficult. Here we demonstrate a simple chemical strategy for achieving high-performance blue phosphors, based on confining isolated chromophores in ionic crystals. Formation of high-density ionic bonds between the cations of ionic crystals and the carboxylic acid groups of the chromophores leads to a segregated molecular arrangement with negligible inter-chromophore interactions. We show that tunable phosphorescence from blue to deep blue with a maximum phosphorescence efficiency of 96.5% can be achieved by varying the charged chromophores and their counterions. Moreover, these phosphorescent materials enable rapid, high-throughput data encryption, fingerprint identification and afterglow display. This work will facilitate the design of high-efficiency blue organic phosphors and extend the domain of organic phosphorescence to new applications.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Organic Light-Emitting Diodes Research · Perovskite Materials and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (31)

Show source-provided references
1. Xu, H. et al. Recent progress in metal–organic complexes for optoelectronic applications. Chem. Soc. Rev. 43, 3259–3302 (2014).10.1039/C3CS60449G ↗
2. Pan, M., Liao, W., Yin, S., Sun, S. & Su, C. Single-phase white-light-emitting and photoluminescent color-tuning coordination assemblies. Chem. Rev. 118, 8889–8935 (2018).10.1021/acs.chemrev.8b00222 ↗
3. Zhang, K. et al. Long-lived emissive probes for time-resolved photoluminescence bioimaging and biosensing. Chem. Rev. 118, 1770–1839 (2018).10.1021/acs.chemrev.7b00425 ↗
4. Deng, W. et al. 2D Ruddlesden–Popper perovskite nanoplate based deep-blue light-emitting diodes for light communication. Adv. Funct. Mater. 29, 1903861–1903869 (2019).10.1002/adfm.201903861 ↗
5. Nanishi, Y. The birth of the blue LED. Nat. Photon. 8, 884–886 (2014).10.1038/nphoton.2014.291 ↗
6. Li, Y., Gecevicius, M. & Qiu, J. Long persistent phosphors—from fundamentals to applications. Chem. Soc. Rev. 45, 2090–2136 (2016).10.1039/C5CS00582E ↗
7. Baldo, M. et al. Highly efficient phosphorescent emission from organic electroluminescent devices. Nature 395, 151–154 (1998).10.1038/25954 ↗
8. Hirata, S. et al. Highly efficient blue electroluminescence based on thermally activated delayed fluorescence. Nat. Mater. 14, 330–336 (2015).10.1038/nmat4154 ↗
9. Yang, J. et al. The influence of the molecular packing on the room temperature phosphorescence of purely organic luminogens. Nat. Commun. 9, 840 (2018).10.1038/s41467-018-03236-6 ↗
10. Shoji, Y. et al. Unveiling a new aspect of simple arylboronic esters: long-lived room-temperature phosphorescence from heavy-atom-free molecules. J. Am. Chem. Soc. 139, 2728–2733 (2017).10.1021/jacs.6b11984 ↗
11. Yang, Z. et al. Intermolecular electronic coupling of organic units for efficient persistent room-temperature phosphorescence. Angew. Chem. Int. Ed. 55, 2181–2185 (2016).10.1002/anie.201509224 ↗
12. An, Z. et al. Stabilizing triplet excited states for ultralong organic phosphorescence. Nat. Mater. 14, 685–690 (2015).10.1038/nmat4259 ↗
13. Lucenti, E. et al. Cyclic triimidazole derivatives: intriguing examples of multiple emissions and ultralong phosphorescence at room temperature. Angew. Chem. Int. Ed. 56, 16302–16307 (2017).10.1002/anie.201710279 ↗
14. Bolton, O., Lee, K., Kim, H., Lin, K. & Kim, J. Activating efficient phosphorescence from purely organic materials by crystal design. Nat. Chem. 3, 205–210 (2011).10.1038/nchem.984 ↗
15. Wei, J. et al. Induction of strong long-lived room-temperature phosphorescence of N-phenyl-2-naphthylamine molecules by confinement in a crystalline dibromobiphenyl matrix. Angew. Chem. Int. Ed. 55, 15589–15593 (2016).10.1002/anie.201607653 ↗
16. Ma, X., Xu, C., Wang, J. & Tian, H. Amorphous pure organic polymers for heavy-atom-free efficient room-temperature phosphorescence emission. Angew. Chem. Int. Ed. 57, 10854–10858 (2018).10.1002/anie.201803947 ↗
17. Cai, S. et al. Enabling long-lived organic room temperature phosphorescence in polymers by subunit interlocking. Nat. Commun. 10, 4247 (2019).10.1038/s41467-019-11749-x ↗
18. Kabe, R. & Adachi, C. Organic long persistent luminescence. Nature 550, 384–387 (2017).10.1038/nature24010 ↗
19. Su, Y. et al. Ultralong room temperature phosphorescence from amorphous organic materials toward confidential information encryption and decryption. Sci. Adv. 4, 9732–9743 (2018).10.1126/sciadv.aas9732 ↗
20. Zhang, G., Palmer, G., Dewhirst, M. & Fraser, C. A dual-emissive-materials design concept enables tumour hypoxia imaging. Nat. Mater. 8, 747–751 (2009).10.1038/nmat2509 ↗
21. Gao, R., Mei, X., Yan, D., Liang, R. & Wei, M. Nano-photosensitizer based on layered double hydroxide and isophthalic acid for singlet oxygenation and photodynamic therapy. Nat. Commun. 9, 2798 (2018).10.1038/s41467-018-05223-3 ↗
22. He, Z. et al. Achieving persistent, efficient, and robust room-temperature phosphorescence from pure organics for versatile applications. Adv. Mater. 31, 1807222 (2019).10.1002/adma.201807222 ↗
23. Hirata, S. Recent advances in materials with room-temperature phosphorescence: photophysics for triplet exciton stabilization. Adv. Optical Mater. 5, 1700116 (2017).10.1002/adom.201700116 ↗
24. Kenry, C. C. & Liu, B. Enhancing the performance of pure organic room-temperature phosphorescent luminophores. Nat. Commun. 10, 2111 (2019).10.1038/s41467-019-10033-2 ↗
25. Baryshnikov, G., Minaev, B. & Agren, H. Theory and calculation of the phosphorescence phenomenon. Chem. Rev. 117, 6500–6537 (2017).10.1021/acs.chemrev.7b00060 ↗
26. Kwon, M. et al. Suppressing molecular motions for enhanced room-temperature phosphorescence of metal-free organic materials. Nat. Commun. 6, 8947 (2015).10.1038/ncomms9947 ↗
27. Sternlicht, H., Nieman, G. & Robinson, G. Triplet–triplet annihilation and delayed fluorescence in molecular aggregates. J. Chem. Phys. 38, 1326–1335 (1963).10.1063/1.1733853 ↗
28. Schulman, E. & Parker, R. Room temperature phosphorescence of organic compounds. The effects of moisture, oxygen, and the nature of the support-phosphor interaction. J. Phys. Chem. 81, 1932–1939 (1977).10.1021/j100535a010 ↗
29. Schulman, E. & Walling, C. Phosphorescence of adsorbed ionic organic molecules at room temperature. Science 178, 53–54 (1972).10.1126/science.178.4056.53 ↗
30. Braga, D., Grepioni, F. & Desiraju, G. Crystal engineering and organometallic architecture. Chem. Rev. 98, 1375–1405 (1998).10.1021/cr960091b ↗
31. Gu, L. et al. Colour-tunable ultra-long organic phosphorescence of a single-component molecular crystal. Nat. Photon. 13, 406–411 (2019).10.1038/s41566-019-0408-4 ↗