journal article·2021-06-09

A Wide Bandgap Polymer Donor Composed of Benzodithiophene and Oxime-Substituted Thiophene for High-Performance Organic Solar Cells

Keqiang He, Pankaj Kumar, Yi Yuan, Zhifang Zhang, Xu Li, Haitao Liu, Jinliang Wang, Yuning Li

ACS Applied Materials & Interfaces· Volume 13· Issue 22
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Abstract

Oxime-substituted thiophene (TO) is used as an acceptor (A) unit to copolymerize with the benzodithiophene (BDT) donor (D) unit to form a novel D–A polymer donor, PBDTTO, which has a low-lying highest occupied molecular orbital energy level (EHOMO) of −5.60 eV and a wide bandgap of 2.03 eV, forming complementary absorption and matching energy levels with the narrow bandgap nonfullerene acceptors. Organic solar cells using PBDTTO and Y6 as the donor and acceptor, respectively, exhibited a JSC of 27.03 mA cm–2, a VOC of 0.83 V, and a fill factor of 0.59, reaching a high power conversion efficiency of 13.29%. The unencapsulated devices show good long-term stability in ambient air. Compared with the acceptor monomers used in other high-performance BDT-based D–A polymer donors, which are synthesized tediously in low yields, the TO acceptor monomer can be conveniently synthesized in only two steps with a high overall yield of 70%. These results demonstrate that TO unit can be used as a promising acceptor unit for developing BDT-based D–A polymer donors at low cost while maintaining high photovoltaic performance.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Perovskite Materials and Applications · Conducting polymers and applications

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

Affiliations

Department of Chemical Engineering and Waterloo Institute for Nanotechnology (WIN), University of Waterloo, 200 University Avenue West, Waterloo, Ontario N2L 3G1, Canada

Institute of Chemistry, Henan Academy of Sciences, 56 Hongzhuan Road, Jinshui District, Zhengzhou, Henan 450002A, China

Funding

Natural Sciences and Engineering Research Council of Canada · Henan Academy of Sciences China

References (72)

Show source-provided references
1. 10.1126/science.270.5243.178910.1126/science.270.5243.1789 ↗
2. 10.1021/acs.chemrev.5b0009810.1021/acs.chemrev.5b00098 ↗
3. 10.1021/jacs.0c0408410.1021/jacs.0c04084 ↗
4. 10.1002/adma.20190801510.1002/adma.201908015 ↗
5. 10.1016/j.spmi.2020.10654910.1016/j.spmi.2020.106549 ↗
6. 10.1002/adma.20160028110.1002/adma.201600281 ↗
7. 10.1002/adma.20140431710.1002/adma.201404317 ↗
8. 10.1038/nmat506310.1038/nmat5063 ↗
9. 10.1016/j.joule.2019.01.00410.1016/j.joule.2019.01.004 ↗
10. 10.1002/adma.20190820510.1002/adma.201908205 ↗
11. 10.1002/anie.20180629110.1002/anie.201806291 ↗
12. 10.1126/science.aat261210.1126/science.aat2612 ↗
13. 10.1039/C9EE02531F10.1039/C9EE02531F ↗
14. 10.1002/adfm.20190983710.1002/adfm.201909837 ↗
15. 10.1039/C7CS00892A10.1039/C7CS00892A ↗
16. 10.1002/aenm.20190099910.1002/aenm.201900999 ↗
17. 10.1002/adfm.20200045610.1002/adfm.202000456 ↗
18. 10.1002/anie.20180897610.1002/anie.201808976 ↗
19. 10.1002/adma.20180649910.1002/adma.201806499 ↗
20. 10.1002/adma.20190458510.1002/adma.201904585 ↗
21. 10.1002/solr.20190000510.1002/solr.201900005 ↗
22. 10.1007/s11426-019-9457-510.1007/s11426-019-9457-5 ↗
23. 10.1002/marc.20190007410.1002/marc.201900074 ↗
24. 10.1039/D0MA00790K10.1039/D0MA00790K ↗
25. 10.1039/C6TA09325F10.1039/C6TA09325F ↗
26. 10.1039/C7TA07228G10.1039/C7TA07228G ↗
27. 10.1038/s41427-019-0163-510.1038/s41427-019-0163-5 ↗
28. 10.1021/acs.chemrev.6b0017610.1021/acs.chemrev.6b00176 ↗
29. 10.1021/jacs.7b0267710.1021/jacs.7b02677 ↗
30. 10.1007/s11426-019-9669-310.1007/s11426-019-9669-3 ↗
31. 10.1021/cm060259210.1021/cm0602592 ↗
32. 10.1021/ja067879o10.1021/ja067879o ↗
33. 10.1021/ma800820r10.1021/ma800820r ↗
34. 10.1021/cm301105610.1021/cm3011056 ↗
35. 10.1002/adma.20090352810.1002/adma.200903528 ↗
36. 10.1002/adma.20130147610.1002/adma.201301476 ↗
37. 10.1021/ma301900h10.1021/ma301900h ↗
38. 10.1002/adma.20150211010.1002/adma.201502110 ↗
39. 10.1021/acs.chemmater.8b0167710.1021/acs.chemmater.8b01677 ↗
40. 10.1002/adma.20170715010.1002/adma.201707150 ↗
41. 10.1039/C9CC02904D10.1039/C9CC02904D ↗
42. 10.1021/acsmacrolett.9b0036810.1021/acsmacrolett.9b00368 ↗
43. 10.1021/acs.macromol.9b0123310.1021/acs.macromol.9b01233 ↗
44. 10.1021/ma501894w10.1021/ma501894w ↗
45. 10.1039/C8EE00151K10.1039/C8EE00151K ↗
46. 10.1021/acs.macromol.0c0154810.1021/acs.macromol.0c01548 ↗
47. 10.1016/j.synthmet.2016.11.02610.1016/j.synthmet.2016.11.026 ↗
48. 10.1002/anie.20180003510.1002/anie.201800035 ↗
49. 10.1002/marc.20170050510.1002/marc.201700505 ↗
50. 10.1002/chem.20120143710.1002/chem.201201437 ↗
51. 10.1039/C4TA01739K10.1039/C4TA01739K ↗
52. 10.1002/pola.2878110.1002/pola.28781 ↗
53. 10.1021/jacs.7b0160610.1021/jacs.7b01606 ↗
54. 10.1021/jacs.8b0269510.1021/jacs.8b02695 ↗
55. 10.1038/nmat503510.1038/nmat5035 ↗
56. 10.1016/j.scib.2020.01.00110.1016/j.scib.2020.01.001 ↗
57. 10.1007/s11426-019-9599-110.1007/s11426-019-9599-1 ↗
58. 10.1039/C9EE01890E10.1039/C9EE01890E ↗
59. 10.1002/adma.20120287310.1002/adma.201202873 ↗
60. 10.1002/adma.20200116010.1002/adma.202001160 ↗
61. 10.1021/acs.macromol.0c0040510.1021/acs.macromol.0c00405 ↗
62. 10.1016/j.joule.2019.03.02010.1016/j.joule.2019.03.020 ↗
63. 10.1016/j.solmat.2017.11.02710.1016/j.solmat.2017.11.027 ↗
64. 10.1002/adfm.20050021110.1002/adfm.200500211 ↗
65. 10.1039/C8EE03608J10.1039/C8EE03608J ↗
66. 10.1002/aenm.20170056610.1002/aenm.201700566 ↗
67. 10.1002/solr.20200007410.1002/solr.202000074 ↗
68. 10.1021/acs.chemmater.7b0377010.1021/acs.chemmater.7b03770 ↗
69. 10.1021/acs.chemrev.9b0004410.1021/acs.chemrev.9b00044 ↗
70. 10.1002/adfm.20200578710.1002/adfm.202005787 ↗
71. 10.1021/ja512318210.1021/ja5123182 ↗
72. 10.1021/jacs.5b1073510.1021/jacs.5b10735 ↗