journal article·2021-03-23

Naphthalenothiophene Imide-Based Polymer Donor for High-Performance Polymer Solar Cells

Haijun Ning, Gongya Zhang, Hui Chen, Zhuoran Wang, Shaofei Ni, Fushen Lu, Fan Liu, Li Dang, Jiangang Liu, Feng He, Qinghe Wu

Chemistry of Materials· Volume 33· Issue 6
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Abstract

Naphthalenothiophene imide (NTI), bearing six-membered imide and a five-membered aromatic ring, was synthesized by a one-step Suzuki reaction in high yield. NTI is an electron-deficient monomer that could effectively lower the HOMO energy level of the polymer. Thus, the NTI-based polymer PNTB1 has a low-lying HOMO energy level (−5.42 eV) without introducing any F or Cl group into the polymer backbone. By mixing with a nonfullerene electron acceptor Y6, solar cell devices exhibit power conversion efficiency as high as 15.18%. Because of the high efficiency of the NTI-based polymer and avoidance of multi-step synthesis of introducing other electron-accepting groups into the polymer chain, the electron-deficient NTI is a promising building unit for high-performance polymer donors.
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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 and Key Laboratory for Preparation and Application of Ordered Structural Materials of Guangdong Province, Shantou University, Shantou, Guangdong 515063, China

Shenzhen Grubbs Institute and Department of Chemistry, Southern University of Science and Technology, Shenzhen 518055, China

Department Guangdong Provincial Laboratory of Chemistry and Fine Chemical Engineering, Shantou University, Shantou 515063, China

Funding

Shantou University · National Natural Science Foundation of China

References (36)

Show source-provided references
1. 10.1021/acs.chemmater.0c0045910.1021/acs.chemmater.0c00459 ↗
2. 10.1039/C8TA06392C10.1039/C8TA06392C ↗
3. 10.1021/acs.chemrev.6b0017610.1021/acs.chemrev.6b00176 ↗
4. 10.1021/acs.chemrev.5b0009810.1021/acs.chemrev.5b00098 ↗
5. 10.1021/acs.chemmater.9b0332710.1021/acs.chemmater.9b03327 ↗
6. 10.1038/s41566-018-0104-910.1038/s41566-018-0104-9 ↗
7. 10.1039/C7CS00892A10.1039/C7CS00892A ↗
8. 10.1021/acsenergylett.9b0207110.1021/acsenergylett.9b02071 ↗
9. 10.1038/natrevmats.2018.310.1038/natrevmats.2018.3 ↗
10. 10.1007/s11426-019-9457-510.1007/s11426-019-9457-5 ↗
11. 10.1021/jacs.8b0402710.1021/jacs.8b04027 ↗
12. 10.1021/jacs.8b1365310.1021/jacs.8b13653 ↗
13. 10.1016/j.joule.2019.01.00410.1016/j.joule.2019.01.004 ↗
14. 10.1038/s41467-019-10351-510.1038/s41467-019-10351-5 ↗
15. 10.1021/acs.chemmater.0c0124510.1021/acs.chemmater.0c01245 ↗
16. 10.1021/acsmacrolett.9b0036810.1021/acsmacrolett.9b00368 ↗
17. 10.1002/adfm.20180882810.1002/adfm.201808828 ↗
18. 10.1016/j.scib.2020.01.00110.1016/j.scib.2020.01.001 ↗
19. 10.1021/ja201131h10.1021/ja201131h ↗
20. 10.1002/adma.20190187210.1002/adma.201901872 ↗
21. 10.1002/adma.20150211010.1002/adma.201502110 ↗
22. 10.1021/jacs.8b1293710.1021/jacs.8b12937 ↗
23. 10.1002/advs.20160003210.1002/advs.201600032 ↗
24. 10.1021/ja111259510.1021/ja1112595 ↗
25. 10.1002/anie.20100545110.1002/anie.201005451 ↗
26. 10.1021/acsaem.8b0050610.1021/acsaem.8b00506 ↗
27. 10.1038/s41560-018-0263-410.1038/s41560-018-0263-4 ↗
28. 10.1002/adma.20130147610.1002/adma.201301476 ↗
29. 10.1038/s41467-018-03207-x10.1038/s41467-018-03207-x ↗
30. 10.1016/j.progpolymsci.2017.03.00310.1016/j.progpolymsci.2017.03.003 ↗
31. 10.1016/j.mattod.2018.02.00310.1016/j.mattod.2018.02.003 ↗
32. 10.1021/acs.chemrev.7b0053510.1021/acs.chemrev.7b00535 ↗
33. 10.1021/jacs.6b0356210.1021/jacs.6b03562 ↗
34. 10.1002/adma.20150057710.1002/adma.201500577 ↗
35. 10.1002/aenm.20180135210.1002/aenm.201801352 ↗
36. 10.1038/s41563-018-0128-z10.1038/s41563-018-0128-z ↗