High‐Efficiency Polymer Light‐Emitting Devices with Robust Phosphorescent Platinum(II) Emitters Containing Tetradentate Dianionic O∧N∧C∧N Ligands
Source abstract
Abstract
[Pt(O∧N∧C∧N)]-type complexes are used as single emitters in solution-processed PLEDs with maximum EQEs of 15.55% for green and 12.73% for white devices, which are the highest values ever achieved for PLEDs based on Pt(ii) complexes. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Light-Emitting Diodes Research · Organic Electronics and Photovoltaics · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Synthetic Chemistry Institute of Molecular Functional Materials and Department of Chemistry The University of Hong Kong Pokfulam Road Hong Kong SAR China
State Key Laboratory on Integrated Optoelectronics College of Electronic Science and Engineering Jilin University Changchun 130012 China
HKU Shenzhen Institute of Research and Innovation Shenzhen 518053 China
References (34)
Show source-provided references
1. 10.1038/347539a010.1038/347539a0 ↗
2. 10.1021/ja021115110.1021/ja0211151 ↗
3. 10.1002/adma.20030623010.1002/adma.200306230 ↗
4. 10.1039/b816352a10.1039/b816352a ↗
5. 10.1364/OL.35.00243610.1364/OL.35.002436 ↗
6. 10.1002/adma.20110275810.1002/adma.201102758 ↗
7. 10.1016/j.orgel.2010.12.00610.1016/j.orgel.2010.12.006 ↗
8. 10.1002/adma.20090063810.1002/adma.200900638 ↗
9. 10.1016/j.jphotochemrev.2011.01.00110.1016/j.jphotochemrev.2011.01.001 ↗
10. 10.1002/adma.20110475810.1002/adma.201104758 ↗
11. 10.1002/adma.20120212310.1002/adma.201202123 ↗
12. 10.1002/asia.20120114610.1002/asia.201201146 ↗
13. 10.1038/2595410.1038/25954 ↗
14. 10.1038/nature0464510.1038/nature04645 ↗
15. 10.1002/adma.20120460210.1002/adma.201204602 ↗
16. 10.1021/ja031777610.1021/ja0317776 ↗
17. 10.1002/1521-3765(20011001)7:19<4180::AID-CHEM4180>3.0.CO;2-910.1002/1521-3765(20011001)7:19<4180::AID-CHEM4180>3.0.CO;2-9 ↗
18. 10.1021/ja039727o10.1021/ja039727o ↗
19. 10.1063/1.12305510.1063/1.123055 ↗
20. 10.1039/c0jm01159b10.1039/c0jm01159b ↗
21. 10.1021/om050343b10.1021/om050343b ↗
22. 10.1021/ic061566c10.1021/ic061566c ↗
23. 10.1039/b904382a10.1039/b904382a ↗
24. 10.1016/0010-8545(91)84019-210.1016/0010-8545(91)84019-2 ↗
25. 10.1021/ic00122a01510.1021/ic00122a015 ↗
26. 10.1021/ic960137j10.1021/ic960137j ↗
27. 10.1016/j.orgel.2010.09.01210.1016/j.orgel.2010.09.012 ↗
28. 10.1021/cm101314b10.1021/cm101314b ↗
29. 10.1002/chem.20120368710.1002/chem.201203687 ↗
30. 10.1039/c2cc37862k10.1039/c2cc37862k ↗
31. 10.1364/OL.37.00110910.1364/OL.37.001109 ↗
32. 10.1063/1.272267510.1063/1.2722675 ↗
33. 10.1002/adma.20060217410.1002/adma.200602174 ↗
34. 10.1063/1.370245210.1063/1.3702452 ↗