journal article·2013-05-22

Traps in Regioregular Poly(3-hexylthiophene) and its Blend with [6,6]-Phenyl-C61-Butyric Acid Methyl Ester for Polymer Solar Cells

Cheng-Yen Yu, Tzu-Hao Jen, Show-An Chen

Publisher page

Abstract

Thermally stimulated current (TSC) technique is used to characterize traps in the regioregular poly(3-hexylthiophene) (rr-P3HT) and its blend with [6,6]-phenyl-C61-butyric acid methyl ester (PCBM). A hole trap in bulk rr-P3HT and an interfacial hole trap located at indium tin oxide (ITO)/rr-P3HT interface are revealed from the TSC measurement. Besides, molecular oxygen (O2) can form a deep electron trap with an onset of detrapping temperature at 225 K in rr-P3HT, in which O2 is located at the main chain region and the detrapping process is induced by chain motions under elevated temperature. In the blend of rr-P3HT:PCBM (1:1 w/w), additional hole trap states are generated in this blend system as compared to those of pure rr-P3HT and PCBM; however, these hole trap states can be reduced by thermal or solvent annealing approaches. Similar to rr-P3HT, a deep electron trap with an onset of detrapping temperature at 250 K can be formed in the blend after O2 exposure. In the case of low PCBM content in the blend (rr-P3HT:PCBM weight ratio of 4:1), an additional electron trap is generated.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Molecular Junctions and Nanostructures

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

Affiliations

Chemical Engineering Department and Frontier Research Center on Fundamental and Applied Sciences of Matters, National Tsing-Hua University, No. 101, Section 2, Kuang-Fu Road, Hsinchu, Taiwan, 30013, Republic of China

References (37)

Show source-provided references
1. He Z. · Nat. Photon. · 2012 · 6 · 593
2. Li G. · Nat. Mater. · 2005 · 4 · 86410.1038/nmat1500 ↗
3. Reyes-Reyes M. · Org. Lett. · 2005 · 7 · 574910.1021/ol051950y ↗
4. Coakley K. M. · Chem. Mater. · 2004 · 16 · 453310.1021/cm049654n ↗
5. Malm N. V. · J. Appl. Phys. · 2001 · 89 · 555910.1063/1.1362371 ↗
6. Malm N. V. · J. Appl. Phys. · 2002 · 92 · 756410.1063/1.1522489 ↗
7. Meier M. · J. Appl. Phys. · 1998 · 84 · 8710.1063/1.368004 ↗
8. Alagiriswamy A. A. · Synth. Met. · 2001 · 116 · 29710.1016/S0379-6779(00)00471-9 ↗
9. Stallinga P. · Phys. B · 1999 · 273 · 92310.1016/S0921-4526(99)00555-4 ↗
10. Schafferhans J. · Appl. Phys. Lett. · 2008 · 93 · 09330310.1063/1.2978237 ↗
11. Nikitenko V. R. · J. Appl. Phys. · 2003 · 94 · 248010.1063/1.1595707 ↗
12. Schafferhans J. · Org. Electron. · 2010 · 11 · 169310.1016/j.orgel.2010.07.016 ↗
13. Baumann A. · Adv. Funct. Mater. · 2011 · 21 · 168710.1002/adfm.201002358 ↗
14. Kawano K. · Adv. Funct. Mater. · 2009 · 19 · 393410.1002/adfm.200901573 ↗
15. Frenkel J. · Phys. Rev. · 1938 · 54 · 64710.1103/PhysRev.54.647 ↗
16. Fang Z. · Mater. Sci. Eng., B · 1990 · 5 · 39710.1016/0921-5107(90)90104-J ↗
17. Ke W. J. · J. Mater. Chem. · 2011 · 21 · 1348310.1039/c1jm12019k ↗
18. Hsieh C. H. · J. Am. Chem. Soc. · 2010 · 132 · 488710.1021/ja100236b ↗
19. Nardes A. M. · Org. Electron. · 2008 · 9 · 72710.1016/j.orgel.2008.05.006 ↗
20. Narioka S. · Appl. Phys. Lett. · 1995 · 67 · 189910.1063/1.114370 ↗
21. Tseng H. E. · Appl. Phys. Lett. · 2003 · 82 · 408610.1063/1.1579557 ↗
22. Tseng H. E. · Appl. Phys. Lett. · 2006 · 88 · 04211210.1063/1.2168042 ↗
23. Chen S. A. · Macromolecules · 1993 · 26 · 281010.1021/ma00063a027 ↗
24. Dudognon E. · Macromolecules · 2001 · 34 · 398810.1021/ma001634t ↗
25. Sauer B. B. · Macromolecules · 1997 · 30 · 332310.1021/ma9608582 ↗
26. Correia N. T. · J. Phys. Chem. B · 2001 · 105 · 566310.1021/jp0044126 ↗
27. Choulis S. A. · Appl. Phys. Lett. · 2004 · 85 · 389010.1063/1.1805175 ↗
28. Schafferhans J. · Adv. Energy Mater. · 2011 · 1 · 65510.1002/aenm.201100175 ↗
29. Matsushima T. · Appl. Phys. Lett. · 2007 · 91 · 10350510.1063/1.2779240 ↗
30. Tsoi W. C. · Macromolecules · 2011 · 44 · 294410.1021/ma102841e ↗
31. Padinger F. · Adv. Funct. Mater. · 2003 · 13 · 8510.1002/adfm.200390011 ↗
32. Ma W. · Adv. Funct. Mater. · 2005 · 15 · 161710.1002/adfm.200500211 ↗
33. Zhokhavets U. · Thin Solid Films · 2006 · 496 · 67910.1016/j.tsf.2005.09.093 ↗
34. Marsh R. A. · Nano Lett. · 2010 · 10 · 92310.1021/nl9038289 ↗
35. Mihailetchi V. D. · Adv. Funct. Mater. · 2006 · 16 · 69910.1002/adfm.200500420 ↗
36. Kumar A. · Adv. Funct. Mater. · 2010 · 20 · 272910.1002/adfm.201000374 ↗
37. Servaites J. D. · Energy Environ. Sci. · 2011 · 4 · 441010.1039/c1ee01663f ↗