journal article·2011-10-26

Diketopyrrolopyrrole-Based π-Bridged Donor–Acceptor Polymer for Photovoltaic Applications

Wenting Li, Taegweon Lee, Soong Ju Oh, Cherie R. Kagan

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Abstract

We report the synthesis, properties, and photovoltaic applications of a new conjugated copolymer (C12DPP-π-BT) containing a donor group (bithiophene) and an acceptor group (2,5-didodecylpyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione), bridged by a phenyl group. Using cyclic voltammetry, we found the energy levels of C12DPP-π-BT are intermediate to common electron donor and acceptor photovoltaic materials, poly (3-hexylthiophene-2,5-diyl) (P3HT) and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM), respectively. Whereas P3HT and PCBM are exclusively electron donating or accepting, we predict C12DPP-π-BT may uniquely serve as either an electron donor or an acceptor when paired with PCBM or P3HT forming junctions with large built-in potentials. We confirmed the ambipolar nature of C12DPP-π-BT in space charge limited current measurements and in C12DPP-π-BT:PCBM and C12DPP-π-BT:P3HT bulk heterojunction solar cells, achieving power conversion efficiencies of 1.67% and 0.84%, respectively, under illumination of AM 1.5G (100 mW/cm(2)). Adding diiodooctane to C12DPP-π-BT:PCBM improved donor-acceptor inter-mixing and film uniformity, and therefore enhanced charge separation and overall device efficiency. Using higher-molecular-weight polymer C12DPP-π-BT in both C12DPP-π-BT:PCBM and C12DPP-π-BT:P3HT devices improved charge transport and hence the performance of the solar cells. In addition, we compared the structural and electronic properties of C12DPP-π-BT:PCBM and C12DPP-π-BT:P3HT blends, representing the materials classes of polymer:fullerene and polymer:polymer blends. In C12DPP-π-BT:PCBM blends, higher short circuit currents were obtained, consistent with faster charge transfer and balanced electron and hole transport, but lower open circuit voltages may be reduced by trap-assisted recombination and interfacial recombination losses. In contrast, C12DPP-π-BT:P3HT blends exhibit higher open circuit voltage, but short circuit currents were limited by charge transfer between the polymers. In conclusion, C12DPP-π-BT is a promising material with intrinsic ambipolar characteristics for organic photovoltaics and may operate as either a donor or acceptor in the design of bulk heterojunction solar cells.
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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

Department of Chemistry, ‡Department of Materials Science and Engineering, and §Department of Electrical and Systems Engineering, University of Pennsylvania, Philadelphia, Pennsylvania 19104

References (67)

Show source-provided references
1. Bijleveld J. C. · J. Am. Chem. Soc. · 2009 · 131 · 1661610.1021/ja907506r ↗
2. Günes S. · Chem. Rev. · 2007 · 107 · 132410.1021/cr050149z ↗
3. Hou J. · J. Am. Chem. Soc. · 2009 · 131 · 1558610.1021/ja9064975 ↗
4. Park S. H. · Nat. Photonics · 2009 · 3 · 29710.1038/nphoton.2009.69 ↗
5. Walker B. · Adv. Funct. Mater. · 2009 · 19 · 306310.1002/adfm.200900832 ↗
6. Li G. · Nat. Mater. · 2005 · 4 · 86410.1038/nmat1500 ↗
7. Yu C.-Y. · Chem. Mater. · 2009 · 21 · 326210.1021/cm9007798 ↗
8. Peng Q. · J.Phys. Chem. B · 2008 · 112 · 280110.1021/jp7105428 ↗
9. Wienk M. M. · Adv. Mater. · 2008 · 20 · 255610.1002/adma.200800456 ↗
10. Chen L. · J.Phys. Chem. C · 2011 · 115 · 1128210.1021/jp201104s ↗
11. Shi M.-M. · J. Polym. Sci., Part A: Polym. Chem. · 2011 · 49 · 145310.1002/pola.24567 ↗
12. Sun S. S. · 2005
13. Chan W. K. · J. Am. Chem. Soc. · 1993 · 115 · 1173510.1021/ja00078a012 ↗
14. Bao Z. · J. Am. Chem. Soc. · 1995 · 117 · 1242610.1021/ja00155a007 ↗
15. Behnke M. · Langmuir · 2002 · 18 · 381510.1021/la011773j ↗
16. Beyerlein T. · Synth. Met. · 2002 · 130 · 11510.1016/S0379-6779(02)00058-9 ↗
17. Zhu Y. · Macromol. Chem. Phys. · 2009 · 210 · 43110.1002/macp.200800507 ↗
18. Zhou E. · Chem. Mater. · 2009 · 21 · 405510.1021/cm901487f ↗
19. Karsten B. P. · Macromol. Rapid Commun. · 2010 · 31 · 155410.1002/marc.201000133 ↗
20. de Leeuw D. M. · Synth. Met. · 1997 · 87 · 5310.1016/S0379-6779(97)80097-5 ↗
21. Huo L. · Macromolecules · 2009 · 42 · 656410.1021/ma9012972 ↗
22. Li Y. · Adv. Mater. · 2010 · 22 · 486210.1002/adma.201002313 ↗
23. Zhou E. · Macromolecules · 2009 · 43 · 82110.1021/ma902398q ↗
24. Li Y. · J. Am. Chem. Soc. · 2011 · 133 · 219810.1021/ja1085996 ↗
25. Coulson D. R. · Inorg. Syn. · 1972 · 13 · 12110.1002/9780470132449.ch23 ↗
26. Kozma E. · Polymer · 2010 · 51 · 226410.1016/j.polymer.2010.03.040 ↗
27. Murphy A. R. · Chem. Mater. · 2005 · 17 · 489210.1021/cm050911d ↗
28. Rabindranath A. R. · Macromolecules · 2006 · 39 · 825010.1021/ma061024e ↗
29. Wu M.-C. · Sol. Energy Mater. Sol. Cells · 2009 · 93 · 86910.1016/j.solmat.2008.10.006 ↗
30. Brabec C. J. · Adv. Funct. Mater. · 2001 · 11 · 37410.1002/1616-3028(200110)11:5<374::AID-ADFM374>3.0.CO;2-W ↗
31. Gregg B. A. · J.Phys. Chem. B · 2003 · 107 · 468810.1021/jp022507x ↗
32. Moliton A. · Polym. Int. · 2006 · 55 · 58310.1002/pi.2038 ↗
33. Pommerehne J. · Adv. Mater. · 1995 · 7 · 55110.1002/adma.19950070608 ↗
34. Cardona C. M. · Adv. Mater. · 2011 · 23 · 236710.1002/adma.201004554 ↗
35. Brabec C. · 200810.1002/9783527623198 ↗
36. Lof R. W. · Phys. Rev. Lett. · 1992 · 68 · 392410.1103/PhysRevLett.68.3924 ↗
37. Veldman D. · Adv. Funct. Mater. · 2009 · 19 · 193910.1002/adfm.200900090 ↗
38. Park Y. · Appl. Phys. Lett. · 1996 · 68 · 269910.1063/1.116313 ↗
39. Eremina N. · Theor. Exp. Chem. · 2009 · 45 · 6310.1007/s11237-009-9065-x ↗
40. Tengstedt C. · Thin Solid Films · 2006 · 515 · 208510.1016/j.tsf.2006.07.005 ↗
41. Scharber M. C. · Adv. Mater. · 2006 · 18 · 78910.1002/adma.200501717 ↗
42. Davis R. J. · J. Mater. Chem. · 2011 · 21 · 172110.1039/C0JM02349C ↗
43. Rand B. P. · Phys. Rev. B · 2007 · 75 · 11532710.1103/PhysRevB.75.115327 ↗
44. Aernouts T. V., P. · Mater. Res. Soc. Symp. Proc. · 2007 · 1013
45. Sariciftci N. S. · Science · 1992 · 258 · 147410.1126/science.258.5087.1474 ↗
46. Koeppe R. · Progr Colloid Polym Sci · 2008 · 135 · 16
47. Hideo O. · J. Photon. Energy · 2011 · 1 · 01111810.1117/1.3569105 ↗
48. Bakulin A. A. · Adv. Funct. Mater. · 2010 · 20 · 165310.1002/adfm.200902099 ↗
49. Chen L.-M. · Adv. Mater. · 2009 · 21 · 143410.1002/adma.200802854 ↗
50. Gur I. · Nano Lett. · 2006 · 7 · 40910.1021/nl062660t ↗
51. Peet J. · Adv. Mater. · 2009 · 21 · 152110.1002/adma.200802559 ↗
52. Chen L.-M. · J. Mater. Chem. · 2010 · 20 · 257510.1039/b925382c ↗
53. Gedde U. W. · 1995
54. Krause S. · Pure Appl. Chem. · 1986 · 58 · 155310.1351/pac198658121553 ↗
55. Mihailetchi V. D. · Adv. Funct. Mater. · 2005 · 15 · 79510.1002/adfm.200400345 ↗
56. Bozano L. · Appl. Phys. Lett. · 1999 · 74 · 113210.1063/1.123959 ↗
57. Melzer C. · Adv. Funct. Mater. · 2004 · 14 · 86510.1002/adfm.200305156 ↗
58. Murgatroyd P. N. · J. Phys. D: Appl. Phys. · 1970 · 3 · 15110.1088/0022-3727/3/2/308 ↗
59. Matsushima T. · Appl. Phys. Lett. · 2009 · 95 · 20330610.1063/1.3267082 ↗
60. Chiguvare Z. · Phys. Rev. B · 2004 · 70 · 23520710.1103/PhysRevB.70.235207 ↗
61. Bijleveld J. C. · Appl. Phys. Lett. · 2010 · 97 · 07330410.1063/1.3480598 ↗
62. Tengstedt C. · Org. Electron. · 2005 · 6 · 2110.1016/j.orgel.2005.02.001 ↗
63. Pensack R. D. · Phys. Chem. Chem. Phys. · 2009 · 11 · 257510.1039/b817113k ↗
64. Shockley W. · J. Appl. Phys. · 1961 · 32 · 51010.1063/1.1736034 ↗
65. Morana M. · Adv. Funct. Mater. · 2008 · 18 · 175710.1002/adfm.200701428 ↗
66. Mandoc M. M. · Appl. Phys. Lett. · 2007 · 91 · 26350510.1063/1.2821368 ↗
67. Hau S. K. · J. Mater. Chem. · 2008 · 18 · 511310.1039/b808004f ↗