End-cap Group Engineering of a Small Molecule Non-Fullerene Acceptor: The Influence of Benzothiophene Dioxide
Source abstract
Abstract
In this study, a sulfonyl-containing end-capping moiety, benzothiophene dioxide, was selected to prepare the nonfullerene acceptor ITBC. ITBC has an acceptor–donor–acceptor (A-D-A) structure, with indacenodithieno[3,2-b]thiophene (IDTT) as the electron-rich core moiety. The strong electron-withdrawing sulfonyl acceptor units leads to extended UV–vis absorption into the near-IR region and relatively low frontier molecular orbital energy levels (LUMO/HOMO: −4.13 eV/–5.61 eV) with a narrow bandgap of 1.48 eV. These values compare favorably to the well-studied small molecule acceptor 2-(3-oxo-2,3-dihydroinden-1-ylidene)malononitrile end-capped indacenodithieno[3,2-b]thiophene (ITIC). A power conversion efficiency of 4.17% was achieved by fabricating organic solar cells with the fluorinated conjugated polymer FTAZ as the donor and ITBC as the acceptor. These results indicate that benzothiophene dioxide is a novel electron-withdrawing end-capping unit for ITBC, and can be used as an electron acceptor for organic solar cells.
Source: openalex_inverted_index · Quality: baseline
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, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States
State Key Laboratory of Materials-Oriented Chemical Engineering, College of Chemical Engineering, Nanjing Tech University, Nanjing, Jiangsu 210009, P. R. China
Funding
Division of Chemistry · Division of Chemical, Bioengineering, Environmental, and Transport Systems
References (53)
Show source-provided references
1. 10.1002/adma.20160543710.1002/adma.201605437 ↗
2. 10.1002/adma.20160139110.1002/adma.201601391 ↗
3. 10.1021/acs.chemrev.5b0009810.1021/acs.chemrev.5b00098 ↗
4. 10.1021/acs.chemrev.5b0016510.1021/acs.chemrev.5b00165 ↗
5. 10.1002/adma.20180086810.1002/adma.201800868 ↗
6. 10.1002/adma.20120348610.1002/adma.201203486 ↗
7. 10.1039/C5RA17715D10.1039/C5RA17715D ↗
8. 10.1002/aenm.20150106310.1002/aenm.201501063 ↗
9. 10.1002/smll.20170112010.1002/smll.201701120 ↗
10. 10.1038/nmat506310.1038/nmat5063 ↗
11. 10.1038/natrevmats.2018.310.1038/natrevmats.2018.3 ↗
12. 10.1002/aenm.20130078510.1002/aenm.201300785 ↗
13. 10.1002/adma.20170426310.1002/adma.201704263 ↗
14. 10.1021/jacs.7b0160610.1021/jacs.7b01606 ↗
15. 10.1038/ncomms1158510.1038/ncomms11585 ↗
16. 10.1039/C5EE02477C10.1039/C5EE02477C ↗
17. 10.1039/C6TA07368A10.1039/C6TA07368A ↗
18. 10.1073/pnas.180753511510.1073/pnas.1807535115 ↗
19. 10.1039/C7TA02562A10.1039/C7TA02562A ↗
20. 10.1002/adma.20140431710.1002/adma.201404317 ↗
21. 10.1002/adma.20160424110.1002/adma.201604241 ↗
22. 10.1002/aenm.20160250910.1002/aenm.201602509 ↗
23. 10.1002/adma.20160028110.1002/adma.201600281 ↗
24. 10.1021/jacs.6b1275510.1021/jacs.6b12755 ↗
25. 10.1021/acs.chemmater.7b0285310.1021/acs.chemmater.7b02853 ↗
26. 10.1039/C7TA05809H10.1039/C7TA05809H ↗
27. 10.1002/adfm.20170219410.1002/adfm.201702194 ↗
28. 10.1021/jacs.6b0200410.1021/jacs.6b02004 ↗
29. 10.1021/jacs.6b0911010.1021/jacs.6b09110 ↗
30. 10.1021/acs.chemmater.7b0461610.1021/acs.chemmater.7b04616 ↗
31. 10.1002/adma.20170025410.1002/adma.201700254 ↗
32. 10.1039/C7TA02486J10.1039/C7TA02486J ↗
33. 10.1021/jacs.7b0267710.1021/jacs.7b02677 ↗
34. 10.1002/adma.20160277610.1002/adma.201602776 ↗
35. 10.1016/0143-7208(89)85024-710.1016/0143-7208(89)85024-7 ↗
36. 10.1002/ejoc.20120016110.1002/ejoc.201200161 ↗
37. 10.1002/adma.20170014410.1002/adma.201700144 ↗
38. 10.1002/adma.20170212510.1002/adma.201702125 ↗
39. 10.1002/adma.20170471310.1002/adma.201704713 ↗
40. 10.1021/acs.chemmater.8b0222210.1021/acs.chemmater.8b02222 ↗
41. 10.1016/j.polymer.2005.01.00110.1016/j.polymer.2005.01.001 ↗
42. 10.1021/ja111259510.1021/ja1112595 ↗
43. 10.1016/j.crci.2013.10.00410.1016/j.crci.2013.10.004 ↗
44. 10.1002/adma.20100455410.1002/adma.201004554 ↗
45. 10.1021/jacs.8b0269510.1021/jacs.8b02695 ↗
46. 10.1039/C7TA07882J10.1039/C7TA07882J ↗
47. 10.1002/adma.20050171710.1002/adma.200501717 ↗
48. 10.1039/C7QM00547D10.1039/C7QM00547D ↗
49. 10.1039/C8QM00004B10.1039/C8QM00004B ↗
50. 10.1002/adma.20170636310.1002/adma.201706363 ↗
51. 10.1002/aenm.20170314710.1002/aenm.201703147 ↗
52. 10.1021/acs.accounts.6b0025510.1021/acs.accounts.6b00255 ↗
53. 10.1039/C7TC04520D10.1039/C7TC04520D ↗