journal article·2018-08-22

Novel Star-Shaped Helical Perylene Diimide Electron Acceptors for Efficient Additive-Free Nonfullerene Organic Solar Cells

Mingliang Wu, Jian-Peng Yi, Li Chen, Guiying He, Fei Chen, Matthew Y. Sfeir, Jianlong Xia

ACS Applied Materials & Interfaces· Volume 10· Issue 33
Publisher page

Abstract

Two star-shaped helical perylene diimide (PDI) electron acceptors TPDI2 and FTPDI2 were designed and synthesized for nonfullerene organic solar cells (OSCs). The integration of helical PDIs into a three-dimensional structure provides a new strategy to tune the intermolecular interactions, and the as-cast blend films with PTB7-Th show favorable morphology as well as efficient charge transfer and separation, as evidenced by the morphology and femtosecond transient absorption (fs-TA) spectroscopy studies. A trade-off between suppressing the self-aggregation and maintaining the charge-transfer properties was achieved by FTPDI2. Using PTB7-Th as the electron donor, the FTPDI2-based nonfullerene OSCs show a high power conversion efficiency of 8.28%, without the assistance of any additives.
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

School of Chemistry, Chemical Engineering and Life Science, State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070, China

Center for Functional Nanomaterials, Brookhaven National Laboratory, Upton, New York 11973, United States

Funding

Wuhan University of Technology · National Natural Science Foundation of China

References (61)

Show source-provided references
1. 10.1038/ncomms629310.1038/ncomms6293 ↗
2. 10.1002/adma.20100140210.1002/adma.201001402 ↗
3. 10.1002/aenm.20150019510.1002/aenm.201500195 ↗
4. 10.1021/acs.chemmater.6b0486210.1021/acs.chemmater.6b04862 ↗
5. 10.1021/cm504140c10.1021/cm504140c ↗
6. 10.1021/acs.chemrev.7b0053510.1021/acs.chemrev.7b00535 ↗
7. 10.1039/c3ta14236a10.1039/c3ta14236a ↗
8. 10.1002/adma.20130591010.1002/adma.201305910 ↗
9. 10.1039/c4ee03424d10.1039/c4ee03424d ↗
10. 10.1021/ja511060210.1021/ja5110602 ↗
11. 10.1021/acsami.7b1600410.1021/acsami.7b16004 ↗
12. 10.1038/natrevmats.2018.310.1038/natrevmats.2018.3 ↗
13. 10.1038/s41566-018-0104-910.1038/s41566-018-0104-9 ↗
14. 10.1039/c6ta02045c10.1039/c6ta02045c ↗
15. 10.1039/c3ee43041c10.1039/c3ee43041c ↗
16. 10.1021/acs.chemmater.7b0296810.1021/acs.chemmater.7b02968 ↗
17. 10.1039/b925605a10.1039/b925605a ↗
18. 10.1002/adma.20110444710.1002/adma.201104447 ↗
19. 10.1021/ja071760d10.1021/ja071760d ↗
20. 10.1038/ncomms924210.1038/ncomms9242 ↗
21. 10.1002/aenm.20160006010.1002/aenm.201600060 ↗
22. 10.1002/adma.20170030910.1002/adma.201700309 ↗
23. 10.1002/aenm.20160166410.1002/aenm.201601664 ↗
24. 10.1021/acs.chemmater.6b0428710.1021/acs.chemmater.6b04287 ↗
25. 10.1002/anie.20161209010.1002/anie.201612090 ↗
26. 10.1021/acsami.6b0392610.1021/acsami.6b03926 ↗
27. 10.1021/cm500633910.1021/cm5006339 ↗
28. 10.1021/acs.chemmater.7b0096410.1021/acs.chemmater.7b00964 ↗
29. 10.1021/acs.chemmater.6b0329210.1021/acs.chemmater.6b03292 ↗
30. 10.1002/adma.20130089710.1002/adma.201300897 ↗
31. 10.1021/acs.chemmater.5b0433910.1021/acs.chemmater.5b04339 ↗
32. 10.1039/c4cc08457h10.1039/c4cc08457h ↗
33. 10.1002/adma.20160099710.1002/adma.201600997 ↗
34. 10.1021/ja509261310.1021/ja5092613 ↗
35. 10.1002/advs.20160011710.1002/advs.201600117 ↗
36. 10.1021/jacs.5b1114910.1021/jacs.5b11149 ↗
37. 10.1002/anie.20160787810.1002/anie.201607878 ↗
38. 10.1021/acs.chemmater.5b0457010.1021/acs.chemmater.5b04570 ↗
39. 10.1021/jacs.7b0914010.1021/jacs.7b09140 ↗
40. 10.1021/jacs.6b1309310.1021/jacs.6b13093 ↗
41. 10.1039/c6cc04229e10.1039/c6cc04229e ↗
42. 10.1021/acs.orglett.8b0054110.1021/acs.orglett.8b00541 ↗
43. 10.1039/c6cc05810h10.1039/c6cc05810h ↗
44. 10.1002/adma.20150401010.1002/adma.201504010 ↗
45. 10.1039/c6ta04232e10.1039/c6ta04232e ↗
46. 10.1021/jacs.6b0436810.1021/jacs.6b04368 ↗
47. 10.1039/c7ta02582c10.1039/c7ta02582c ↗
48. 10.1021/jacs.6b0356210.1021/jacs.6b03562 ↗
49. 10.1039/c6ta09049d10.1039/c6ta09049d ↗
50. 10.1039/c6ta09394a10.1039/c6ta09394a ↗
51. 10.1039/c6ta08739f10.1039/c6ta08739f ↗
52. 10.1039/c6ta08870h10.1039/c6ta08870h ↗
53. 10.1002/advs.20170011010.1002/advs.201700110 ↗
54. 10.1002/adma.20140052510.1002/adma.201400525 ↗
55. 10.1002/asia.20170044010.1002/asia.201700440 ↗
56. 10.1038/nphoton.2015.610.1038/nphoton.2015.6 ↗
57. 10.1038/nphoton.2014.17210.1038/nphoton.2014.172 ↗
58. 10.1021/acs.chemmater.6b0123010.1021/acs.chemmater.6b01230 ↗
59. 10.1039/c5sc04956c10.1039/c5sc04956c ↗
60. 10.1002/adma.20170334410.1002/adma.201703344 ↗
61. 10.1021/jz301883y10.1021/jz301883y ↗