journal article·2024

Tuning the number and position of triphenylamine substituents on a benzo[ b ]furan core to achieve high-efficiency deep-blue and blue emitters

MeiTing Luo, MingXin Wu, BoHua Zhang, XinYe Wang, Yi Chen, QingYu Jia, Dongdong Wang, Lei Gou, Zhaoxin Wu

Journal of Materials Chemistry C· Volume 12· Issue 4
Publisher page

Abstract

The deep-blue to blue emitters, 56dTPA-BF, 356tTPA-BF and 2356fTPA-BF were successfully achieved by using benzo[ b ]furan as central skeleton. The 2356fTPA-BF shows the maximum EQE of 5.32/3.42% with emission peak of 448 nm in doped/non-doped devices.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Organic Electronics and Photovoltaics · Luminescence and Fluorescent Materials

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

Affiliations

School of Chemistry, Xi’an Jiaotong University, Xi’an 710049, P. R. China

Institute of Energy Materials and Device, School of Materials Science and Engineering, Chang’an University, Xi’an 710061, China

Key Laboratory for Physical Electronics and Devices of the Ministry of Education & Shaanxi Key Lab of Information Photonic Technique, School of Electronic and Information Engineering, Xi’an Jiaotong University, Xi’an 710049, P. R. China

Funding

National Natural Science Foundation of China

References (35)

Show source-provided references
1. Baldo · Nature · 1998 · 395 · 15110.1038/25954 ↗
2. Lamansky · J. Am. Chem. Soc. · 2001 · 123 · 430410.1021/ja003693s ↗
3. Zhang · J. Am. Chem. Soc. · 2012 · 134 · 1470610.1021/ja306538w ↗
4. Gibson · Chem. Phys. Chem. · 2016 · 17 · 295610.1002/cphc.201600662 ↗
5. Monkman · ACS Appl. Mater. Interfaces · 2022 · 14 · 2046310.1021/acsami.1c09189 ↗
6. Chao · Adv. Mater. · 2005 · 17 · 99210.1002/adma.200401476 ↗
7. Santen · Jpn. J. Appl. Phys. · 2003 · 42 · 111010.1143/JJAP.42.1110 ↗
8. Shinar · J. Phys. D: Appl. Phys. · 2008 · 41 · 13300110.1088/0022-3727/41/13/133001 ↗
9. Muralidharan · Chem. Phys. Lett. · 1992 · 192 · 57110.1016/0009-2614(92)85518-F ↗
10. Li · J. Am. Chem. Soc. · 2017 · 139 · 1726110.1021/jacs.7b09381 ↗
11. Yu · Adv. Opt. Mater. · 2022 · 11 · 220221710.1002/adom.202202217 ↗
12. Figueira-Duarte · Chem. Rev. · 2011 · 111 · 726010.1021/cr100428a ↗
13. Liang · Appl. Phys. Lett. · 2021 · 119 · 04330610.1063/5.0044609 ↗
14. Tang · Org. Electron. · 2006 · 7 · 15510.1016/j.orgel.2006.01.001 ↗
15. Sudyoadsuk · J. Mater. Chem. C · 2021 · 9 · 625110.1039/D1TC00406A ↗
16. Zheng · Adv. Opt. Mater. · 2021 · 9 · 210154510.1002/adom.202100965 ↗
17. Malatong · Dyes Pigm. · 2021 · 184 · 10887410.1016/j.dyepig.2020.108874 ↗
18. Chen · J. Mater. Chem. C · 2023 · 11 · 876710.1039/D3TC01349A ↗
19. Ahn · Nat. Photonics · 2019 · 13 · 54010.1038/s41566-019-0415-5 ↗
20. Suresh · Adv. Mater. · 2023 · 230099710.1002/adma.202300997 ↗
21. Okumoto · Chem. Mater. · 2003 · 15 · 69910.1021/cm020849+ ↗
22. Wong · Org. Lett. · 2005 · 7 · 513110.1021/ol051865q ↗
23. Park · Org. Electron. · 2010 · 11 · 86410.1016/j.orgel.2010.01.030 ↗
24. Yang · J. Mater. Chem. C · 2013 · 1 · 286710.1039/c3tc00734k ↗
25. Goushi · Nat. Photonics · 2012 · 6 · 25310.1038/nphoton.2012.31 ↗
26. Mehes · Angew. Chem., Int. Ed. · 2012 · 51 · 1131110.1002/anie.201206289 ↗
27. Nakagawa · Chem. Commun. · 2012 · 48 · 958010.1039/c2cc31468a ↗
28. Uoyama · Nature · 2012 · 492 · 23410.1038/nature11687 ↗
29. Dias · Methods Appl. Fluoresc. · 2017 · 5 · 01200110.1088/2050-6120/aa537e ↗
30. Volpe · Chem. – Eur. J. · 2015 · 21 · 1019110.1002/chem.201500384 ↗
31. Han · Phosphorus, Sulfur Silicon Relat. Elem. · 2013 · 188 · 159910.1080/10426507.2013.770738 ↗
32. Saini · Eur. J. Org. Chem. · 2017 · 370710.1002/ejoc.201700541 ↗
33. Liu · J. Mater. Chem. C · 2020 · 8 · 688310.1039/D0TC00102C ↗
34. Saragi · Chem. Rev. · 2007 · 107 · 101110.1021/cr0501341 ↗
35. Qian · Org. Electron. · 2012 · 13 · 274110.1016/j.orgel.2012.07.047 ↗