journal article·2013-11-12

Conjugated Polymer-Mediated Polymorphism of a High Performance, Small-Molecule Organic Semiconductor with Tuned Intermolecular Interactions, Enhanced Long-Range Order, and Charge Transport

Jihua Chen, Ming Shao, Kai Xiao, Zhengran He, Dawen Li, Bradley S. Lokitz, Dale K. Hensley, S. Michael Kilbey, John E. Anthony, Jong K. Keum, Adam J. Rondinone, Wen-Ya Lee, Sanghyun Hong, Zhenan Bao

Chemistry of Materials· Volume 25· Issue 21
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Abstract

We use 6,13-bis(triisopropylsilylethynyl)pentacene as a model small molecule organic semiconductor and two conjugated polymer additives to demonstrate conjugated polymer-mediated polymorphism of a small molecule organic semiconductor for the first time. The conjugated polymer additives, used with a slow solution crystallization approach, yield crystal structures that are not accessible by nonconjugated polymer additives and impart excellent long-range order. In both of the small molecule semiconductor/conjugated polymer blends studied here, previously unreported polymorphs of a small molecule semiconductor have been identified which also leads to improved charge transport in the absence of external alignment. These results open up a new exciting avenue to manipulate unit cell structure, long-range order, and charge transport of high performance, solution-processed, small molecule organic semiconductors.
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Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Perovskite Materials and Applications

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

Affiliations

Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States

Department of Electrical and Computer Engineering, Center for Materials For Information Technology, University of Alabama, Tuscaloosa, Alabama 35487, United States

Department of Chemistry, University of Tennessee, Knoxville, Tennessee 37996, United States

Department of Chemistry, University of Kentucky, Lexington, Kentucky 40506, United States

Neutron Scattering Science Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States

Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States

References (38)

Show source-provided references
1. Bernstein J. · 2002
2. Falini G. · Science · 1996 · 271 · 6710.1126/science.271.5245.67 ↗
3. Belcher A. M. · Nature · 1996 · 381 · 5610.1038/381056a0 ↗
4. Price C. P. · J. Am. Chem. Soc. · 2005 · 127 · 551210.1021/ja042561m ↗
5. Lang M. D. · J. Am. Chem. Soc. · 2002 · 124 · 1483410.1021/ja0286526 ↗
6. Hermet P. · J. Phys. Chem. A · 2005 · 109 · 420210.1021/jp050798e ↗
7. Mattheus C. C. · Synth. Met. · 2003 · 138 · 47510.1016/S0379-6779(02)00467-8 ↗
8. Siegrist T. · Angew. Chem., Int. Ed. · 2001 · 40 · 173210.1002/1521-3773(20010504)40:9<1732::AID-ANIE17320>3.0.CO;2-7 ↗
9. Troisi A. · J. Phys. Chem. B · 2005 · 109 · 184910.1021/jp0457489 ↗
10. Coropceanu V. · Chem. Rev. · 2007 · 107 · 92610.1021/cr050140x ↗
11. Fichou D. · J. Mater. Chem. · 2000 · 10 · 57110.1039/a908312j ↗
12. Campione M. · J. Appl. Phys. · 2007 · 101 · 610.1063/1.2718291 ↗
13. Giri G. · Nature · 2011 · 480 · 50410.1038/nature10683 ↗
14. Anthony J. E. · J. Am. Chem. Soc. · 2001 · 123 · 948210.1021/ja0162459 ↗
15. Park S. K. · Appl. Phys. Lett. · 2007 · 91 · 06351410.1063/1.2768934 ↗
16. Chen J. · J. Appl. Phys. · 2008 · 103 · 11451310.1063/1.2936978 ↗
17. Kang J. · J. Am. Chem. Soc. · 2008 · 130 · 1227310.1021/ja804013n ↗
18. Kim D. H. · Adv. Funct. Mater. · 2007 · 19 · 67810.1002/adma.200601259 ↗
19. Sakanoue T. · Nat. Mater. · 2010 · 9 · 73610.1038/nmat2825 ↗
20. Lee W. H. · Appl. Phys. Lett. · 2007 · 90 · 3
21. Kim M. J. · Org. Electron. · 2011 · 12 · 117010.1016/j.orgel.2011.03.034 ↗
22. Chen J. · Org. Electron. · 2009 · 10 · 69610.1016/j.orgel.2009.03.007 ↗
23. Jung H. J. · Adv. Funct. Mater. · 2010 · 20 · 290310.1002/adfm.201000032 ↗
24. Hamilton R. · Adv. Mater. · 2009 · 21 · 116610.1002/adma.200801725 ↗
25. He Z. · Adv. Funct. Mater. · 2011 · 21 · 361710.1002/adfm.201002656 ↗
26. Lada M. · J. Mater. Chem. · 2011 · 21 · 1123210.1039/c1jm11119a ↗
27. Li X. · Adv. Funct. Mater. · 2009 · 19 · 361010.1002/adfm.200901353 ↗
28. Jiang Y. · J. Mater. Chem. · 2012 · 22 · 435610.1039/c2jm15483h ↗
29. Chen J. · J. Mater. Res. · 2007 · 22 · 170110.1557/JMR.2007.0220 ↗
30. Li G. · Adv. Funct. Mater. · 2007 · 17 · 163610.1002/adfm.200600624 ↗
31. Trznadel M. · Macromolecules · 1998 · 31 · 505110.1021/ma970627a ↗
32. Davis R. J. · J. Mater. Chem. · 2011 · 21 · 172110.1039/C0JM02349C ↗
33. Chen J. · J. Phys. Chem. B · 2006 · 110 · 792810.1021/jp0511045 ↗
34. Mannsfeld S. C. B. · Adv. Mater. · 2011 · 23 · 12710.1002/adma.201003135 ↗
35. Robinson L. · Surf. Sci. · 2006 · 600 · 14810.1016/j.susc.2006.03.039 ↗
36. Headrick R. L. · Appl. Phys. Lett. · 2008 · 92 · 310.1063/1.2839394 ↗
37. Yu X. · ACS Nano · 2011 · 5 · 355910.1021/nn2007964 ↗
38. Sirringhaus H. · Nature · 1999 · 401 · 68510.1038/44359 ↗