journal article·2013-12

Investigation of optical and electrical properties of new aromatic polyazomethine with thiophene and cardo moieties toward application in organic solar cells

Agnieszka Iwan, Ewa Schab-Balcerzak, Krzysztof P. Korona, Sylwia Grankowska, Maria Kamińska

Synthetic Metals· Volume 185-186
Publisher page

Abstract

Abstract New polyazomethine (25Th-cardo) based on thiophene and cardo moieties was synthesized, characterized and tested as active layer in solar cells. The structure of polymer was characterized by means of FTIR and 1 H NMR spectroscopy. The temperatures of 5% weight loss of the polyazomethine range from 435 to 455 °C in nitrogen, depending on the heating rate applied. 25Th-cardo has electrochemical energy band gap of approximately ∼1.85 eV, and HOMO energy level at −5.21 eV. Optical absorption properties of pure 25Th-cardo and of its mixtures with [6,6]-phenyl-C 61 -butyric acid methyl ester (PCBM) were investigated on different substrates: glass or glass/PEDOT:PSS. Electrical properties of the two kinds of devices: ITO/25Th-cardo:PCBM/Al and ITO/PEDOT:PSS/25Th-cardo:PCBM/Al were tested by impedance spectroscopy. The investigated polymer solar cells contained different amounts of PCBM. Bulk heterojunction solar cells with the architecture ITO/PEDOT:PSS/25Th-cardo:PCBM/Al gave a power conversion efficiency 3.5 times higher for the mixture of 25Th-cardo to PCBM 1:2 (w/w) than for 1:1 (w/w) under 100 mW/cm 2 AM1.5G sunlight illumination in air. The external quantum efficiency value of 25Th-cardo:PCBM solar cell was the highest (about 0.3%) in the near UV range from 3.1 to 3.7 eV.
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Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Synthesis and properties of polymers

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References (39)

Show source-provided references
1. Iwan · Prog. Polym. Sci. · 2011 · 36 · 127710.1016/j.progpolymsci.2011.05.001 ↗
2. Iwan · Prog. Polym. Sci. · 2008 · 33 · 28910.1016/j.progpolymsci.2007.09.005 ↗
3. Barik · Macromolecules · 2012 · 45 · 116510.1021/ma2024304 ↗
4. Barik · Mater. Chem. Phys. · 2011 · 129 · 52910.1016/j.matchemphys.2011.04.060 ↗
5. Sadavarte · High Perform. Polym. · 2011 · 23 · 49410.1177/0954008311417316 ↗
6. Sek · Macromolecules · 2008 · 41 · 665310.1021/ma702637k ↗
7. Sek · Spectrochim Acta A: Mol. Biomol. Spect. · 2009 · 72 · 110.1016/j.saa.2008.06.022 ↗
8. Niu · Mater. Chem. Phys. · 2004 · 86 · 3310.1016/j.matchemphys.2004.01.023 ↗
9. Niu · Mater. Lett. · 2004 · 58 · 297910.1016/j.matlet.2004.05.007 ↗
10. Palewicz · Energy Procedia · 2011 · 3 · 8410.1016/j.egypro.2011.01.014 ↗
11. Iwan · Opt. Mater. · 2011 · 34 · 6110.1016/j.optmat.2011.07.004 ↗
12. Hindson · J. Mater. Chem. · 2010 · 20 · 93710.1039/B919159C ↗
13. Sharma · Thin Solid Films · 1996 · 278 · 12910.1016/0040-6090(95)08182-8 ↗
14. Iwan · Synt. Met. · 2012 · 162 · 14310.1016/j.synthmet.2011.11.024 ↗
15. Iwan · High Perform. Polym. · 2013
16. Iwan · Synt. Met. · 2010 · 160 · 185610.1016/j.synthmet.2010.06.029 ↗
17. Palewicz · Acta Phys. Polon. A · 2012 · 121 · 43910.12693/APhysPolA.121.439 ↗
18. Jarząbek · J. Non-Cryst. Solids · 2006 · 352 · 166010.1016/j.jnoncrysol.2005.11.107 ↗
19. Weszka · Acta Phys. Polon. A · 2011 · 120 · 93610.12693/APhysPolA.120.936 ↗
20. Bednarski · Acta Phys. Polon. A · 2012 · 122 · 108310.12693/APhysPolA.122.1083 ↗
21. Gąsiorowski · J. Phys. Chem. C · 2013 · 117 · 258410.1021/jp306108f ↗
22. Niu · Polym. Chem. · 2011 · 2 · 280410.1039/c1py00237f ↗
23. Kaczmarczyk · J. Mol. Struct. · 2013 · 1048 · 17910.1016/j.molstruc.2013.05.036 ↗
24. Rusu · Acta Materialia · 2007 · 55 · 43310.1016/j.actamat.2006.07.048 ↗
25. Jarzabek · Thin Solid Films · 1996 · 279 · 20410.1016/0040-6090(95)08162-3 ↗
26. de Leeuw · Synth. Met. · 1997 · 87 · 5310.1016/S0379-6779(97)80097-5 ↗
27. Wang · Tetrahedron · 2007 · 63 · 169510.1016/j.tet.2006.11.058 ↗
28. Dufresne · J. Org. Chem. · 2008 · 73 · 385910.1021/jo8002503 ↗
29. Bourgeaux · Macromolecules · 2007 · 40 · 179210.1021/ma070292p ↗
30. Bundgaard · Sol. Energy Mater. Sol. C · 2007 · 91 · 95410.1016/j.solmat.2007.01.015 ↗
31. Thompson · Angew. Chem. Int. Ed. · 2008 · 47 · 5810.1002/anie.200702506 ↗
32. Cai · Sol. Energy Mater. Sol. C · 2010 · 94 · 11410.1016/j.solmat.2009.10.005 ↗
33. Dennler · Adv. Mater. · 2009 · 21 · 132310.1002/adma.200801283 ↗
34. Park · Nat. Photonic · 2009 · 3 · 29710.1038/nphoton.2009.69 ↗
35. Liu · Appl. Phys. Lett. · 2011 · 99
36. Tamilavan · Polym. Bull. · 2012 · 69 · 43910.1007/s00289-012-0740-z ↗
37. Zhu · Macromolecules · 2007 · 40 · 198110.1021/ma062376o ↗
38. Garcia-Belmonte · Org. Electron. · 2008 · 9 · 84710.1016/j.orgel.2008.06.007 ↗
39. Leever · Adv. Energy Mater. · 2012 · 2 · 12010.1002/aenm.201100357 ↗