journal article·2023-03-09

Efficient Polymer Solar Cells Enabled by A-DA′D-A Type Acceptors with Alkoxypheny-Substituted Quinoxaline as the Fused-Ring Core

Haimei Wu, Baofeng Zhao, Sen Zhang, Zhaozhao Bi, Weiping Wang, Liuchang Wang, Zhiyuan Cong, Wei Ma, Chao Gao

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Abstract

Polymer solar cells (PSCs) have made tremendous advances over the past three years due to the advantages offered by A-DA′D-A type small molecule electron-acceptors (SMEAs). To this day, the power conversion efficiencies (PCEs) have exceeded 19% in the PSCs incorporated by appropriate wide-bandgap polymer electron-donors and structure fine-tuned A-DA′D-A SMEAs. Despite high fill factor (FF) and short-circuit current ( J SC ) that were successfully achieved in wide-bandgap polymers and these type SMEA-based PSCs, the open-circuit voltage ( V OC ) was comparatively small, which hinders the performance further enhancement of PSCs. To boost the V OC of A-DA′D-A type SMEA-based PSCs, two small molecules ( BQ-4F and BQ-4Cl ) were designed and synthesized, with the alkoxyphenyl-substituted quinoxaline-containing fused core as the A′ unit and difluorinated and dichlorinated end groups as the A segments. Benefiting from the introduced alkoxyphenyl-substituted quinoxaline-containing fused core, the two SMEAs all have elevated lowest unoccupied molecular orbital energy levels. PSCs based on PM6: BQ-4F achieved a high V OC of 0.916 V and a promising PCE of 12.45%. Despite the device of PM6: BQ-4Cl realizing a slightly decreased V OC of 0.906 V, it accomplished high J SC (22.47 mA cm –2 ) and FF (66.2%), thus giving rise to a high efficiency of 13.48%. Besides, after adding 20% of these two small molecules in PM6:Y6-based devices, the fabricated BQ-4F - and BQ-4Cl -based ternary devices achieved high PCEs of 16.75% and 16.77%, respectively, which were superior to the 15.81% value of the PM6:Y6 binary PSC. The findings from this study should assist in the design and construction of new quinoxaline-based A-DA′D-A SMEAs that would be used for the manufacture of binary and ternary PSCs with high V OC and efficiencies.
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

Xi’an Key Laboratory of Liquid Crystal and Organic Photovoltaic Materials, State Key Laboratory of Fluorine & Nitrogen Chemicals, Xi’an Modern Chemistry Research Institute, No. 168 of East Zhangba Road, Xi’an 710065, China

State Key Laboratory for Mechanical Behavior of Materials, Xi’an Jiaotong University, No. 28 of West Xianning Road, Xi’an 710049, China

School of Chemical Engineering, Xi’an University, No. 168 of South Taibai Road, Xi’an 710065, China

Funding

National Natural Science Foundation of China · Natural Science Foundation of Shaanxi Province · Higher Education Discipline Innovation Project · Key Research and Development Projects of Shaanxi Province

References (53)

Show source-provided references
1. 10.1021/acs.accounts.5b0036310.1021/acs.accounts.5b00363 ↗
2. 10.1039/C4MH00042K10.1039/C4MH00042K ↗
3. 10.1021/acs.chemrev.1c0095510.1021/acs.chemrev.1c00955 ↗
4. 10.1002/adma.20140431710.1002/adma.201404317 ↗
5. 10.1039/D2CC03172H10.1039/D2CC03172H ↗
6. 10.20517/energymater.2021.0810.20517/energymater.2021.08 ↗
7. 10.1016/j.scib.2020.04.03010.1016/j.scib.2020.04.030 ↗
8. 10.1016/j.scib.2020.08.03010.1016/j.scib.2020.08.030 ↗
9. 10.1016/j.joule.2019.01.00410.1016/j.joule.2019.01.004 ↗
10. 10.1016/j.joule.2021.06.02010.1016/j.joule.2021.06.020 ↗
11. 10.1038/s41563-022-01244-y10.1038/s41563-022-01244-y ↗
12. 10.1002/adma.20210242010.1002/adma.202102420 ↗
13. 10.1002/adma.20210278710.1002/adma.202102787 ↗
14. 10.1002/adma.20220208910.1002/adma.202202089 ↗
15. 10.1016/j.joule.2019.09.01010.1016/j.joule.2019.09.010 ↗
16. 10.1002/adma.20190344110.1002/adma.201903441 ↗
17. 10.1093/nsr/nwz20010.1093/nsr/nwz200 ↗
18. 10.1039/C9CP05015A10.1039/C9CP05015A ↗
19. 10.1038/s41467-019-10351-510.1038/s41467-019-10351-5 ↗
20. 10.1039/C9EE03710A10.1039/C9EE03710A ↗
21. 10.1016/j.joule.2020.02.00410.1016/j.joule.2020.02.004 ↗
22. 10.1039/D1EE01832A10.1039/D1EE01832A ↗
23. 10.1038/s41560-021-00820-x10.1038/s41560-021-00820-x ↗
24. 10.1039/D0TA08830G10.1039/D0TA08830G ↗
25. 10.1021/acsenergylett.2c0220110.1021/acsenergylett.2c02201 ↗
26. 10.1021/acsami.2c0779110.1021/acsami.2c07791 ↗
27. 10.1021/acsami.1c0265210.1021/acsami.1c02652 ↗
28. 10.1021/acsami.7b1099510.1021/acsami.7b10995 ↗
29. 10.1038/s41467-019-08386-910.1038/s41467-019-08386-9 ↗
30. 10.1038/s41566-019-0573-510.1038/s41566-019-0573-5 ↗
31. 10.1002/adma.20150211010.1002/adma.201502110 ↗
32. 10.1038/s41467-018-03207-x10.1038/s41467-018-03207-x ↗
33. 10.1016/j.scib.2020.01.00110.1016/j.scib.2020.01.001 ↗
34. 10.1002/aenm.20170057510.1002/aenm.201700575 ↗
35. 10.1002/adma.20210416110.1002/adma.202104161 ↗
36. 10.1002/adma.20100222510.1002/adma.201002225 ↗
37. 10.1039/C2TC00327A10.1039/C2TC00327A ↗
38. 10.1039/C5TA05096K10.1039/C5TA05096K ↗
39. 10.1021/acsami.7b0394710.1021/acsami.7b03947 ↗
40. 10.1021/jacs.9b0993910.1021/jacs.9b09939 ↗
41. 10.1002/adma.20190632410.1002/adma.201906324 ↗
42. 10.1038/s41467-022-30927-y10.1038/s41467-022-30927-y ↗
43. 10.1021/acsenergylett.2c0158910.1021/acsenergylett.2c01589 ↗
44. 10.1002/cjoc.20180008210.1002/cjoc.201800082 ↗
45. 10.1039/C6TA04030F10.1039/C6TA04030F ↗
46. 10.1021/jacs.5b0594010.1021/jacs.5b05940 ↗
47. 10.1021/ja060141m10.1021/ja060141m ↗
48. 10.1002/aenm.20160014810.1002/aenm.201600148 ↗
49. 10.1002/adma.20060109310.1002/adma.200601093 ↗
50. 10.1021/nn401267s10.1021/nn401267s ↗
51. 10.1016/j.nanoen.2017.07.04410.1016/j.nanoen.2017.07.044 ↗
52. 10.1088/1742-6596/247/1/01200710.1088/1742-6596/247/1/012007 ↗
53. 10.1039/D1EE01864G10.1039/D1EE01864G ↗