Alternative Carrier Injection/Extraction Inspired by Electrode Interlayers Based on Peripheral Modification of the Electron-Rich Skeleton
Source abstract
Abstract
Peripheral modifications of the electron-rich trifluorene-substituted triphenylamine core have been comparatively studied through the linkage of the different polar pendants with fluorene via saturated sp3 hybrid alkyl chains. The work function of electrode could be effectively tuned by the interlayers with or without peripheral pendants of phosphoric acid and phosphonate groups to give selective hole and electron injection/extraction property. Their applications in various vacuum- and solution-processed organic light-emitting diodes and photovoltaic devices were thoroughly investigated. The current comparative study provides valuable exploration on developing high-performance environmentally friendly solvent-processed electrode interlayer materials.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Organic Light-Emitting Diodes Research · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Luminescent Materials and Devices and Institute of Polymer Optoelectronic Materials and Devices, South China University of Technology, Guangzhou 510640, China
Funding
Ministry of Education of the People's Republic of China · Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China · Guandong Natural Science Foundation · Department of Education of Guangdong Province
References (28)
Show source-provided references
1. Kim J. S. · J. Appl. Phys. · 1998 · 84 · 685910.1063/1.368981 ↗
2. Chen D. C. · Appl. Phys. Lett. · 2014 · 104 · 05330410.1063/1.4864622 ↗
3. Kim J. S. · Appl. Phys. Lett. · 1999 · 74 · 308410.1063/1.124069 ↗
4. Kawano K. · Sol. Energy Mater. Sol. Cells · 2006 · 90 · 352010.1016/j.solmat.2006.06.041 ↗
5. Wu S. · Org. Electron. · 2011 · 12 · 50410.1016/j.orgel.2010.12.015 ↗
6. Shao J. · Org. Electron. · 2013 · 14 · 205110.1016/j.orgel.2013.04.041 ↗
7. Su S. J. · Adv. Mater. · 2008 · 20 · 418910.1002/adma.200801375 ↗
8. Su S. J. · Adv. Mater. · 2010 · 22 · 331110.1002/adma.200904249 ↗
9. Yang T. B. · Adv. Energy Mater. · 2012 · 2 · 52310.1002/aenm.201100598 ↗
10. Xu Z. · Adv. Funct. Mater. · 2009 · 19 · 122710.1002/adfm.200801286 ↗
11. He Z. C. · Nat. Photonics · 2012 · 6 · 59110.1038/nphoton.2012.190 ↗
12. Wu H. B. · Adv. Mater. · 2004 · 16 · 182610.1002/adma.200400067 ↗
13. Guan X. · Adv. Funct. Mater. · 2012 · 22 · 284610.1002/adfm.201200199 ↗
14. Duan C. H. · Adv. Mater. · 2011 · 23 · 166510.1002/adma.201004661 ↗
15. Chen D. C. · Macromol. Rapid Commun. · 2013 · 34 · 59510.1002/marc.201200812 ↗
16. Zhou G. · Macromolecules · 2005 · 38 · 541610.1021/ma050807h ↗
17. He Z. C. · Adv. Mater. · 2014 · 26 · 100610.1002/adma.201303391 ↗
18. Zhong S. · J. Appl. Phys. · 2013 · 114 · 11370910.1063/1.4821223 ↗
19. Li C. Z. · Adv. Mater. · 2013 · 25 · 442510.1002/adma.201300580 ↗
20. Zhang B. H. · Appl. Phys. Lett. · 2010 · 97 · 04350610.1063/1.3475021 ↗
21. Bardecker J. A. · Adv. Funct. Mater. · 2008 · 18 · 396410.1002/adfm.200800033 ↗
22. Ghaedi M. · J. Ind. Eng. Chem. · 2014 · 20 · 1710.1016/j.jiec.2013.04.031 ↗
23. Roosta M. · Ultrason. Sonochem. · 2014 · 21 · 24210.1016/j.ultsonch.2013.05.014 ↗
24. Ghaedia M. · J. Ind. Eng. Chem. · 2013 · 19 · 178110.1016/j.jiec.2013.02.020 ↗
25. Vaynzof Y. · Appl. Phys. Lett. · 2008 · 93 · 10330510.1063/1.2980425 ↗
26. Kepler R. G. · Appl. Phys. Lett. · 1995 · 66 · 361810.1063/1.113806 ↗
27. Chen D. C. · Org. Electron. · 2014 · 15 · 119710.1016/j.orgel.2014.03.026 ↗
28. Klenkler A. R. · J. Phys. Chem. C · 2011 · 115 · 1677710.1021/jp2036586 ↗