journal article·2014-05-28

Highly Stable, Solution-Processable Phenothiazine Derivative as Hole Collection Material for Organic Solar Cells

Jen-Hsien Huang, Kuen-Chan Lee

Publisher page

Abstract

In this study, we have synthesized a solution-processable phenothiazine, 4-phenothiazin-10-yl-anisole (APS), as hole collection material in organic solar cells (OSCs). The APS reveals unique optical and electronic properties which can efficiently modify the work function (ΦW) of indium tin oxide (ITO) electrode to enhance the electron blocking capability. Moreover, the results indicate that the APS is highly air-stable which can significantly enhance the long-term stability of OCSs. The inverted device based on APS reached a power conversion efficiency (PCE) of 3.56% and exhibited much better stability under ambient conditions relative to that of the corresponding PEDOT:PSS based device.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Thin-Film Transistor Technologies

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

Affiliations

Department of Green Material Technology, Green Technology Research Institute, CPC Corporation, Kaohsiung 81126, Taiwan

Department of Fragrance and Cosmetic Science, Kaohsiung Medical University, 100 Shih-Chuan First Road, Kaohsiung 80708, Taiwan

References (25)

Show source-provided references
1. Yu G. · Science · 1995 · 270 · 178910.1126/science.270.5243.1789 ↗
2. Halls J. J. M. · Synth. Met. · 1997 · 85 · 130710.1016/S0379-6779(97)80252-4 ↗
3. Padinger F. · Adv. Funct. Mater. · 2003 · 13 · 8510.1002/adfm.200390011 ↗
4. Li G. · Nat. Mater. · 2005 · 4 · 86410.1038/nmat1500 ↗
5. Huang J. H. · Org. Electron. · 2009 · 10 · 2710.1016/j.orgel.2008.09.007 ↗
6. Liang Y. · J. Am. Chem. Soc. · 2009 · 131 · 779210.1021/ja901545q ↗
7. Blouin N. · J. Am. Chem. Soc. · 2008 · 130 · 73210.1021/ja0771989 ↗
8. Huo L. J. · Angew. Chem., Int. Ed. · 2011 · 50 · 969710.1002/anie.201103313 ↗
9. Lee J. K. · J. Am. Chem. Soc. · 2008 · 130 · 361910.1021/ja710079w ↗
10. Li W. · J. Am. Chem. Soc. · 2013 · 135 · 552910.1021/ja401434x ↗
11. You J. · Nat. Commun. · 2013 · 4 · 144610.1038/ncomms2411 ↗
12. You J. · Adv. Mater. · 2013 · 25 · 397310.1002/adma.201300964 ↗
13. Huang J. H. · RSC Adv. · 2012 · 2 · 748710.1039/c2ra20543b ↗
14. Ibrahem M. A. · Sol. Energy Mater. Sol. Cells · 2013 · 108 · 15610.1016/j.solmat.2012.09.007 ↗
15. Shao S. · Adv. Energy Mater. · 2013 · 3 · 34910.1002/aenm.201200609 ↗
16. Fan X. · Adv. Funct. Mater. · 2012 · 22 · 58510.1002/adfm.201102054 ↗
17. Tao C. · Appl. Phys. Lett. · 2009 · 94 · 04331110.1063/1.3076134 ↗
18. Nardes A. M. · Org. Electron. · 2008 · 9 · 72710.1016/j.orgel.2008.05.006 ↗
19. Shelton S. W. · ACS Appl. Mater. Interfaces · 2012 · 4 · 253410.1021/am300228w ↗
20. Wu Y. · ACS Appl. Mater. Interfaces · 2013 · 5 · 1042810.1021/am404053e ↗
21. Ke W. J. · J. Mater. Chem. · 2011 · 21 · 1348310.1039/c1jm12019k ↗
22. Huang J. H. · Org. Electron. · 2009 · 10 · 2710.1016/j.orgel.2008.09.007 ↗
23. Huang J. H. · Sol. Energy Mater. Sol. Cells · 2010 · 94 · 2210.1016/j.solmat.2009.02.019 ↗
24. Huang J. H. · J. Phys. Chem. C · 2011 · 115 · 239810.1021/jp1090894 ↗
25. Huang J. H. · Org. Electron. · 2011 · 12 · 175510.1016/j.orgel.2011.06.017 ↗