journal article·2019-02-12

A Benzobis(thiazole)-Based Copolymer for Highly Efficient Non-Fullerene Polymer Solar Cells

Shuguang Wen, Yi Li, Thomas Rath, Yonghai Li, Yao Wu, Xichang Bao, Liangliang Han, Heike Ehmann, Gregor Trimmel, Yong Zhang, Renqiang Yang

Chemistry of Materials· Volume 31· Issue 3
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Abstract

In recent years, non-fullerene polymer solar cells have attracted much attention due to their great potential for achieving high power conversion efficiencies, and in addition to the already existing donor polymers, varieties of excellent acceptors have been developed. To further improve the performance, the main challenge is now to identify perfect donor–acceptor pairs with suitable electronic properties and complementary optical absorption. In this article, we have investigated a donor–acceptor alternating copolymer poly[(4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b:4,5-b′]dithiophene)-2,6-diyl-alt-(2,6-bis(5-bromo-4-(2-butyloctyl) thiophen-2-yl)benzo[1,2-d:4,5-d′]bis(thiazole))] with benzo[1,2-d:4,5-d′]bis(thiazole) (BBT) as the accepting unit and benzo[1,2-b:4,5-b′]dithiophene as the donor unit. The polymer shows a wide band gap of 2.1 eV with absorption peaks at 515 and 554 nm, matching well with the strongest region of the solar radiation spectrum. A blend of this polymer with the narrow-bandgap acceptor ITIC-F, (3,9-bis(2-methylene-(3-(1,1-dicyanomethylene)-6-fluoro-indanone))-5,5,11,11-tetrakis(4-hexylphenyl)-dithieno[2,3-d:2′,3′-d′]-s-indaceno[1,2-b:5,6-b′]dithiophene)(mixture with 7-fluoro-indanone isomer), as the active layer in combination with a solvent vapor annealing process led to solar cells exhibiting a high efficiency of 13.3% with an open-circuit voltage of 0.91 V, a short current density of 20.9 mA cm–2, and a fill factor of 0.70. The solvent vapor annealing method led to an improvement of the molecular packing, exciton dissociation, and charge transport, thus enhancing the power conversion efficiency. It is noteworthy that external quantum efficiency spectra show excellent photoresponse, especially in the wavelength range from 430 to 570 nm, demonstrating that this donor–acceptor combination efficiently absorbs in the wavelength range where the solar radiation spectrum has its maximum. The results indicate that polymers based on BBT are very promising candidates for high-performance non-fullerene polymer solar cells.
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Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Fullerene Chemistry and Applications

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

Affiliations

CAS Key Laboratory of Bio-based Materials, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao 266101, China

Laboratory of Nanophotonic Functional Materials and Devices, Institute of Optoelectronic Materials and Technology, South China Normal University, Guangzhou 510631, China

Institute for Chemistry and Technology of Materials (ICTM), NAWI Graz, Graz University of Technology, Stremayrgasse 9, 8010 Graz, Austria

Anton Paar GmbH, Anton-Paar-Straße 20, 8054 Graz, Austria

Funding

Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China · OeAD-GmbH · Department of Science and Technology of Shandong Province

References (47)

Show source-provided references
1. 10.1126/science.332.6027.29310.1126/science.332.6027.293 ↗
2. 10.1021/ar200244610.1021/ar2002446 ↗
3. 10.1126/science.270.5243.178910.1126/science.270.5243.1789 ↗
4. 10.1021/acs.chemrev.5b0009810.1021/acs.chemrev.5b00098 ↗
5. 10.1038/natrevmats.2017.4310.1038/natrevmats.2017.43 ↗
6. 10.1038/nphoton.2012.1110.1038/nphoton.2012.11 ↗
7. 10.1021/cr900182s10.1021/cr900182s ↗
8. Dominguez I. F. · Adv. Energy Mater. · 2017 · 7 · 160132010.1002/aenm.201601320 ↗
9. 10.1002/adma.20140431710.1002/adma.201404317 ↗
10. 10.1038/ncomms1365110.1038/ncomms13651 ↗
11. 10.1002/adma.20170390610.1002/adma.201703906 ↗
12. 10.1002/adfm.20170219410.1002/adfm.201702194 ↗
13. 10.1021/jacs.7b0117010.1021/jacs.7b01170 ↗
14. 10.1002/adma.20170520810.1002/adma.201705208 ↗
15. 10.1021/jacs.7b1127810.1021/jacs.7b11278 ↗
16. 10.1021/acs.chemrev.7b0053510.1021/acs.chemrev.7b00535 ↗
17. 10.1002/adma.20150380110.1002/adma.201503801 ↗
18. 10.1002/adma.20170490410.1002/adma.201704904 ↗
19. 10.1021/jacs.7b1323910.1021/jacs.7b13239 ↗
20. 10.1002/adma.20170451010.1002/adma.201704510 ↗
21. 10.1002/anie.20161094410.1002/anie.201610944 ↗
22. 10.1021/ja511060210.1021/ja5110602 ↗
23. 10.1016/j.synthmet.2017.12.00510.1016/j.synthmet.2017.12.005 ↗
24. 10.1021/jacs.6b0174410.1021/jacs.6b01744 ↗
25. 10.1002/adma.20170397310.1002/adma.201703973 ↗
26. 10.1002/adma.20160415510.1002/adma.201604155 ↗
27. 10.1002/aenm.20160074210.1002/aenm.201600742 ↗
28. 10.1021/jacs.7b0160610.1021/jacs.7b01606 ↗
29. 10.1002/adma.20170229110.1002/adma.201702291 ↗
30. 10.1002/adma.20180086810.1002/adma.201800868 ↗
31. 10.1002/adma.20170483710.1002/adma.201704837 ↗
32. 10.1002/adma.20160028110.1002/adma.201600281 ↗
33. 10.1021/acs.macromol.5b0274210.1021/acs.macromol.5b02742 ↗
34. 10.1002/ejoc.20120162910.1002/ejoc.201201629 ↗
35. 10.1021/ma201128x10.1021/ma201128x ↗
36. 10.1021/ma901527810.1021/ma9015278 ↗
37. 10.1002/pola.2779310.1002/pola.27793 ↗
38. 10.1002/adma.20100211710.1002/adma.201002117 ↗
39. 10.1021/acsami.7b1061910.1021/acsami.7b10619 ↗
40. 10.1021/ma061206910.1021/ma0612069 ↗
41. 10.1039/C7QM00025A10.1039/C7QM00025A ↗
42. 10.1002/cjoc.20180001510.1002/cjoc.201800015 ↗
43. 10.1039/c4ee00022f10.1039/c4ee00022f ↗
44. 10.1021/nn102295p10.1021/nn102295p ↗
45. 10.1063/1.188924010.1063/1.1889240 ↗
46. 10.1002/adfm.20160114410.1002/adfm.201601144 ↗
47. 10.1039/C6TA07201A10.1039/C6TA07201A ↗