Small-molecule acceptors based on 4H-cyclopenta[1,2-b:5,4-b′]dithiophene units with near-infrared absorption for nonfullerene polymer solar cells
Source abstract
Abstract
Abstract Two small-molecule acceptors 1CIC and 2CIC based on 4H-cyclopenta[1,2-b:5,4-b′]dithiophene units and 1,1-dicyanomethylene-3-indanone were developed. Compared with 1CIC, 2CIC possesses red-shift absorption, higher HOMO and LUMO energy levels, and higher electron mobility. Nonfullerene polymer solar cells based on PTB7-Th:2CIC gave a power conversion efficiency (PCE) of 3.53%, with an open-circuit voltage (Voc) of 0.75 V, a short-circuit current (Jsc) of 10.97 mA/cm2. As contrast, PTB7-Th:1CIC cell gave a PCE of 0.26%. Our results indicated that the absorption spectra of small-molecule acceptors containing indaceno[1,2-b:5,6-b′]dithiophene (IDT) core can be efficiently extended to near-infrared region by replacing the aromatic benzene ring of with 2,2′-bithiophene.
Source: openaire · Quality: candidate unverified · Source record ↗
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.
References (38)
Show source-provided references
1. Yu · Science · 1995 · 270 · 178910.1126/science.270.5243.1789 ↗
2. Cheng · Chem. Rev. · 2009 · 109 · 586810.1021/cr900182s ↗
3. Cui · Adv. Energy Mater. · 2017 · 7 · 160125110.1002/aenm.201601251 ↗
4. He · Phys. Chem. Chem. Phys. · 2011 · 13 · 197010.1039/C0CP01178A ↗
5. Xiao · Energy Environ. Sci. · 2016 · 9 · 211410.1039/C6EE01026A ↗
6. Yan · Nat. Rev. Mater. · 2018 · 3 · 1800310.1038/natrevmats.2018.3 ↗
7. Lin · Adv. Mater. · 2015 · 27 · 117010.1002/adma.201404317 ↗
8. Li · Phys. Chem. Chem. Phys. · 2017 · 19 · 344010.1039/C6CP07465K ↗
9. Yuan · Nano Energy · 2016 · 30 · 31210.1016/j.nanoen.2016.10.008 ↗
10. Zhang · Acta Phys.-Chim. Sin. · 2017 · 33 · 2327
11. Qiu · Adv. Mater. · 2017 · 29 · 160496410.1002/adma.201604964 ↗
12. Liu · J. Am. Chem. Soc. · 2017 · 139 · 335610.1021/jacs.7b00566 ↗
13. Wang · Adv. Mater. · 2017 · 29 · 170130810.1002/adma.201701308 ↗
14. Zhu · Adv. Mater. · 2018 · 30 · 170471310.1002/adma.201704713 ↗
15. Li · Adv. Mater. · 2018 · 30 · 170596910.1002/adma.201705969 ↗
16. Xiao · Sci. Bull. · 2017 · 62 · 156210.1016/j.scib.2017.11.003 ↗
17. Lin · J. Am. Chem. Soc. · 2016 · 138 · 297310.1021/jacs.6b00853 ↗
18. Dai · J. Am. Chem. Soc. · 2017 · 139 · 133610.1021/jacs.6b12755 ↗
19. Wang · Adv. Mater. · 2017 · 29 · 170212510.1002/adma.201702125 ↗
20. Li · Nano Energy · 2016 · 27 · 43010.1016/j.nanoen.2016.07.019 ↗
21. Xu · Adv. Mater. · 2017 · 29 · 170451010.1002/adma.201704510 ↗
22. Li · Macromolecules · 2013 · 46 · 549710.1021/ma4009302 ↗
23. Kumar · J. Mater. Chem. A · 2015 · 3 · 489210.1039/C4TA05807K ↗
24. Zhang · Dyes Pigments · 2017 · 141 · 26210.1016/j.dyepig.2017.02.015 ↗
25. Li · J. Phys. Chem. B · 2010 · 114 · 446110.1021/jp101222s ↗
26. Li · Adv. Mater. · 2018 · 30 · 170520810.1002/adma.201705208 ↗
27. Lin · Adv. Energy Mater. · 2016 · 6 · 160085410.1002/aenm.201600854 ↗
28. Pommerehne · Adv. Mater. · 1995 · 7 · 55110.1002/adma.19950070608 ↗
29. Cao · Energy Environ. Sci. · 2013 · 6 · 322410.1039/c3ee41948g ↗
30. Tan · Macromolecules · 2013 · 46 · 11310.1021/ma302243r ↗
31. Ma · Chem. Mater. · 2017 · 29 · 794210.1021/acs.chemmater.7b02887 ↗
32. Jiao · Sci. China Chem. · 2017 · 60 · 25110.1007/s11426-016-0244-3 ↗
33. Li · Synth. Met. · 2017 · 226 · 7110.1016/j.synthmet.2017.02.003 ↗
34. Zhang · Synth. Met. · 2016 · 211 · 12110.1016/j.synthmet.2015.11.017 ↗
35. Yuan · Chem. Commun. · 2016 · 52 · 688110.1039/C6CC01771A ↗
36. Liu · Adv. Mater. · 2016 · 28 · 849010.1002/adma.201602857 ↗
37. Liu · Synth. Met. · 2017 · 227 · 12210.1016/j.synthmet.2017.03.013 ↗
38. Zhang · Adv. Sci. · 2017 · 4 · 170015210.1002/advs.201700152 ↗