journal article·2013-01-09

Tailor-Made Additives for Morphology Control in Molecular Bulk-Heterojunction Photovoltaics

Kenneth R. Graham, Romain Stalder, Patrick M. Wieruszewski, Dinesh G. Patel, Danielle H. Salazar, John R. Reynolds

Publisher page

Abstract

Tailor-made additives, which are molecules that share the same molecular structure as a parent molecule with only slight structural variations, have previously been demonstrated as a useful means to control crystallization dynamics in solution. For example, tailor-made additives can be added to solutions of a crystallizing parent molecule to alter the crystal growth rate, size, and shape. We apply this strategy as a means to predictably control morphology in molecular bulk-heterojunction (BHJ) photovoltaic cells. Through the use of an asymmetric oligomer substituted with a bulky triisobutylsilyl end group, the morphology of BHJ blends can be controlled resulting in a near doubling (from 1.3 to 2.2%) in power conversion efficiency. The use of tailor-made additives provides promising opportunities for controlling crystallization dynamics, and thereby film morphologies, for many organic electronic devices such as photovoltaics and field-effect transistors.
Source: openalex_inverted_index · Quality: baseline

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

The George and Josephine Butler Polymer Research Laboratory, Department of Chemistry and Center for Macromolecular Science and Engineering, University of Florida, Gainesville, Florida 32611-7200, United States

School of Chemistry and Biochemistry, School of Materials Science and Engineering, and Center for Organic Photonics and Electronics, Georgia Institute of Technology, Atlanta, Georgia 30332-0400, United States

References (51)

Show source-provided references
1. Chen H.-Y. · Nat. Photonics · 2009 · 3 · 64910.1038/nphoton.2009.192 ↗
2. Zhou H. · Angew. Chem., Int. Ed. · 2011 · 50 · 299510.1002/anie.201005451 ↗
3. He Z. · Adv. Mater. · 2011 · 23 · 463610.1002/adma.201103006 ↗
4. Small C. E. · Nat. Photonics · 2011 · 6 · 11510.1038/nphoton.2011.317 ↗
5. Li Z. · Adv. Energy Mater. · 2011 · 2 · 7410.1002/aenm.201100572 ↗
6. Sun Y. · Nat. Mater. · 2012 · 11 · 4410.1038/nmat3160 ↗
7. Walker B. · Adv. Funct. Mater. · 2009 · 19 · 306310.1002/adfm.200900832 ↗
8. Loser S. · J. Am. Chem. Soc. · 2011 · 133 · 814210.1021/ja202791n ↗
9. Shang H. · Adv. Mater. · 2011 · 23 · 155410.1002/adma.201004445 ↗
10. Scully S. R. · J. Appl. Phys. · 2006 · 100 · 3490710.1063/1.2226687 ↗
11. Lunt R. R. · J. Appl. Phys. · 2009 · 105 · 05371110.1063/1.3079797 ↗
12. Shaw P. E. · Adv. Mater. · 2008 · 20 · 351610.1002/adma.200800982 ↗
13. Ma W. · Adv. Funct. Mater. · 2005 · 15 · 161710.1002/adfm.200500211 ↗
14. Savenije T. J. · Adv. Funct. Mater. · 2005 · 15 · 126010.1002/adfm.200400559 ↗
15. Li G. · Adv. Funct. Mater. · 2007 · 17 · 163610.1002/adfm.200600624 ↗
16. Miller S. · J. Mater. Chem. · 2008 · 18 · 30610.1039/B713926H ↗
17. Peet J. · Nat. Mater. · 2007 · 6 · 49710.1038/nmat1928 ↗
18. Corey V. H. · Adv. Mater. · 2010 · 22 · E6310.1002/adma.200903677 ↗
19. Walker B. · Adv. Energy Mater. · 2011 · 1 · 22110.1002/aenm.201000054 ↗
20. Winzenberg K. N. · Chem. Mater. · 2009 · 21 · 570110.1021/cm9028337 ↗
21. Krebs F. C. · J. Mater. Chem. · 2009 · 19 · 544210.1039/b823001c ↗
22. Shaheen S. E. · Appl. Phys. Lett. · 2001 · 79 · 299610.1063/1.1413501 ↗
23. Hoth C. N. · Nano Lett. · 2008 · 8 · 280610.1021/nl801365k ↗
24. Roncali J. · Adv. Energy Mater. · 2011 · 1 · 14710.1002/aenm.201000008 ↗
25. Darling S. B. · Energy Environ. Sci. · 2009 · 2 · 126610.1039/b912086f ↗
26. Miyanishi S. · Chem. Commun. · 2010 · 46 · 672310.1039/c0cc01819h ↗
27. Zhang F. · Adv. Mater. · 2001 · 13 · 187110.1002/1521-4095(200112)13:24<1871::AID-ADMA1871>3.0.CO;2-3 ↗
28. Sivula K. · Adv. Mater. · 2006 · 18 · 20610.1002/adma.200501787 ↗
29. Sary N. · Adv. Mater. · 2010 · 22 · 76310.1002/adma.200902645 ↗
30. Lee J. U. · J. Mater. Chem. · 2010 · 20 · 328710.1039/b923752f ↗
31. Eckert J.-F. · J. Am. Chem. Soc. · 2000 · 122 · 746710.1021/ja9941072 ↗
32. Bu L. · J. Am. Chem. Soc. · 2009 · 131 · 1324210.1021/ja905980w ↗
33. 10.1002/adfm.20120110010.1002/adfm.201201100 ↗
34. Addadi L. · Angew. Chem., Int. Ed. · 1985 · 24 · 46610.1002/anie.198504661 ↗
35. Berkovitch-Yellin Z. · J. Am. Chem. Soc. · 1985 · 107 · 311110.1021/ja00297a017 ↗
36. Weissbuch I. · Science · 1991 · 253 · 63710.1126/science.253.5020.637 ↗
37. Lechuga-Ballesteros D. · J. Colloid Interface Sci. · 1993 · 157 · 14710.1006/jcis.1993.1169 ↗
38. Garnier S. · J. Cryst. Growth · 2002 · 234 · 20710.1016/S0022-0248(01)01608-6 ↗
39. van Enckevort W. J. P. · J. Phys. Chem. C · 2008 · 112 · 638010.1021/jp7099543 ↗
40. Oliveira D. · J. Cryst. Growth · 2010 · 312 · 43110.1016/j.jcrysgro.2009.11.028 ↗
41. Lee B. S. S. · Adv. Mater. · 2009 · 21 · 360510.1002/adma.200900705 ↗
42. Fraboni B. · Adv. Mater. · 2009 · 21 · 183510.1002/adma.200802904 ↗
43. Mei J. · Org. Lett. · 2010 · 12 · 66010.1021/ol902512x ↗
44. Amb C. M. · J. Am. Chem. Soc. · 2011 · 133 · 1006210.1021/ja204056m ↗
45. Bozano L. · Appl. Phys. Lett. · 1999 · 74 · 113210.1063/1.123959 ↗
46. Scott J. C. · Synth. Met. · 2000 · 111 · 28910.1016/S0379-6779(99)00449-X ↗
47. Bisquert J. · Phys. Status Solidi A · 2006 · 203 · 376210.1002/pssa.200622248 ↗
48. Graham K. R. · Adv. Funct. Mater. · 2012 · 22 · 480110.1002/adfm.201102456 ↗
49. Xu Z. · Adv. Funct. Mater. · 2009 · 19 · 122710.1002/adfm.200801286 ↗
50. Wang H. · Chem. Mater. · 2011 · 23 · 202010.1021/cm200320u ↗
51. Vandewal K. · Phys. Rev. B · 2010 · 81 · 110.1103/PhysRevB.81.125204 ↗