journal article·2013-08-28

Enhancing the Performance of Polymer Photovoltaic Cells by Using an Alcohol Soluble Fullerene Derivative as the Interfacial Layer

Qiang Mei, Cuihong Li, Xue Gong, Heng Lu, Enquan Jin, Chun Du, Zhen Lu, Li Jiang, Xiangyue Meng, Chunru Wang, Zhishan Bo

Publisher page

Abstract

Alcohol soluble fullerene derivative (FN-C60) has been synthesized and used as a cathode interfacial layer for high-efficiency polymer solar cells (PSCs). To examine the function of the FN-C60 interfacial layer, polymer solar cells were fabricated with blends of P3:PC71BM, HXS-1:PC71BM, PDFCDTBT:PC71BM, and PDPQTBT:PC71BM as the active layer. In comparison to the bare Al electrode, power conversion efficiencies (PCEs) of P3:PC71BM, HXS-1:PC71BM, PDFCDTBT:PC71BM, and PDPQTBT:PC71BM based PSCs were increased from 3.50 to 4.64%, 4.69 to 5.25%, 2.70 to 4.60%, and 1.52 to 2.29%, respectively, when FN-C60/Al was used as the electrode. Moreover, the overall photovoltaic performances of PSCs with the FN-C60/Al electrode were better than those of cells with LiF/Al electrode, indicating that FN-C60 is a potential interfacial layer material to replace LiF.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Nanowire Synthesis and Applications

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

Affiliations

Beijing Key Laboratory of Energy Conversion and Storage Materials, College of Chemistry, Key Laboratory of Theoretical and Computational Photochemistry, Ministry of Education, Beijing Normal University, Beijing 100875, China

Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China

References (53)

Show source-provided references
1. Yu G. · J. Appl. Phys. · 1995 · 78 · 451010.1063/1.359792 ↗
2. Kim J. Y. · Science · 2007 · 317 · 22210.1126/science.1141711 ↗
3. Hou J. H. · J. Am. Chem. Soc. · 2008 · 130 · 1614410.1021/ja806687u ↗
4. Chen J. W. · Acc. Chem. Res. · 2009 · 42 · 170910.1021/ar900061z ↗
5. Krebs F. C. · Sol. Energ. Mat. Sol. C. · 2009 · 93 · 39410.1016/j.solmat.2008.10.004 ↗
6. Brabec C. J. · Adv. Mater. · 2010 · 22 · 383910.1002/adma.200903697 ↗
7. Zhan X. W. · Polym. Chem. · 2010 · 1 · 40910.1039/B9PY00325H ↗
8. Gendron D. · Energ. Environ. Sci. · 2011 · 4 · 122510.1039/c1ee01072g ↗
9. He Z. C. · Adv. Mater. · 2011 · 23 · 463610.1002/adma.201103006 ↗
10. Dou L. T. · J. Am. Chem. Soc. · 2012 · 134 · 1007110.1021/ja301460s ↗
11. Li W. W. · J. Am. Chem. Soc. · 2012 · 134 · 1378710.1021/ja305358z ↗
12. Small C. E. · Nat. Photonics · 2012 · 6 · 11510.1038/nphoton.2011.317 ↗
13. Qin R. P. · J. Am. Chem. Soc. · 2009 · 131 · 1461210.1021/ja9057986 ↗
14. Li W. · Polymer · 2010 · 51 · 303110.1016/j.polymer.2010.05.015 ↗
15. Du C. · Macromolecules · 2011 · 44 · 761710.1021/ma201477b ↗
16. He Z. C. · Nat. Photonics · 2012 · 6 · 59110.1038/nphoton.2012.190 ↗
17. Heliatek GmbH,Dresden, Germany.http://www.heliatek.com(accessed June 28, 2013) .
18. Brabec C. J. · Adv. Funct. Mater. · 2001 · 11 · 37410.1002/1616-3028(200110)11:5<374::AID-ADFM374>3.0.CO;2-W ↗
19. Brabec C. J. · Thin Solid Films · 2002 · 403 · 36810.1016/S0040-6090(01)01586-3 ↗
20. Mihailetchi V. D. · Appl. Phys. Lett. · 2004 · 85 · 97010.1063/1.1782252 ↗
21. Hau S. K. · Ieee. J. Sel. Top. Quant. · 2010 · 16 · 166510.1109/JSTQE.2010.2047098 ↗
22. Mihailetchi V. D. · J. Appl. Phys. · 2003 · 94 · 684910.1063/1.1620683 ↗
23. Ratcliff E. L. · J. Phys. Chem. Lett. · 2011 · 2 · 133710.1021/jz2002259 ↗
24. Walzer K. · Chem. Rev. · 2007 · 107 · 123310.1021/cr050156n ↗
25. Clarke T. M. · Chem. Rev. · 2010 · 110 · 673610.1021/cr900271s ↗
26. Waldauf C. · Appl. Phys. Lett. · 2006 · 89 · 23351710.1063/1.2402890 ↗
27. White M. S. · Appl. Phys. Lett. · 2006 · 89 · 14351710.1063/1.2359579 ↗
28. Brabec C. J. · Appl. Phys. Lett. · 2002 · 80 · 128810.1063/1.1446988 ↗
29. Hau S. K. · Appl. Phys. Lett. · 2010 · 97 · 25330710.1063/1.3530431 ↗
30. Yip H. L. · Adv. Mater. · 2008 · 20 · 237610.1002/adma.200703050 ↗
31. Tao C. · Appl. Phys. Lett. · 2008 · 93 · 19330710.1063/1.3026741 ↗
32. Goh C. · J. Appl. Phys. · 2007 · 101 · 11450310.1063/1.2737977 ↗
33. Kim J. Y. · Adv. Mater. · 2006 · 18 · 57210.1002/adma.200501825 ↗
34. Park S. H. · Nat. Photonics. · 2009 · 3 · 29710.1038/nphoton.2009.69 ↗
35. Sun Y. M. · Adv. Mater. · 2011 · 23 · 167910.1002/adma.201004301 ↗
36. You J. B. · Adv. Mater. · 2012 · 24 · 526710.1002/adma.201201958 ↗
37. Huang F. · Chem. Soc. Rev. · 2010 · 39 · 250010.1039/b907991m ↗
38. He Z. C. · Adv. Mater. · 2011 · 23 · 308610.1002/adma.201101319 ↗
39. Seo J. H. · J. Am. Chem. Soc. · 2011 · 133 · 841610.1021/ja2037673 ↗
40. Tang Z. · Adv. Mater. · 2012 · 24 · 55410.1002/adma.201104579 ↗
41. Duan C. H. · Chem. Mater. · 2012 · 24 · 168210.1021/cm300824h ↗
42. Lee R. H. · Polym. Adv. Technol. · 2011 · 22 · 211010.1002/pat.1730 ↗
43. Schulze K. · Adv. Mater. · 2006 · 18 · 287210.1002/adma.200600658 ↗
44. Cheng Y. J. · Chem. Mater. · 2011 · 23 · 151210.1021/cm1032404 ↗
45. Hsieh C. H. · J. Am. Chem. Soc. · 2010 · 132 · 488710.1021/ja100236b ↗
46. O’Malley K. M. · Adv. Energy. Mater. · 2012 · 2 · 8210.1002/aenm.201100522 ↗
47. Li C. Z. · J. Mater. Chem. · 2012 · 22 · 857410.1039/c2jm30755c ↗
48. Wang S. · Adv. Funct. Mater. · 2003 · 13 · 46310.1002/adfm.200304339 ↗
49. Zhu B. · Macromolecules · 2007 · 40 · 449410.1021/ma062246f ↗
50. Wei X. W. · J. Chem. Soc. Perkin Trans. 2 · 2002 · 47
51. Jin E. Q. · Macromolecules · 2012 · 45 · 784310.1021/ma301622g ↗
52. Potscavage W. J. · Acc. Chem. Res. · 2009 · 42 · 175810.1021/ar900139v ↗
53. Blom P. W. M. · Adv. Mater. · 2007 · 19 · 155110.1002/adma.200601093 ↗