journal article·2021-07-01Open access

Optoelectronic Properties of a Benzodithiophene-Based Organic Photovoltaic

Yu-Wei Su, Yi-Shan Huang, Ho-Chun Huang, Po-Tuan Chen

Abstract

Benzo[1,2-b:4,5-b′]dithiophene (BDT) contains electron donating groups and conjugates with acceptor material as a donor-acceptor type conjugated polymer, which can be applied in bulk heterojunction organic photovoltaics due to its high charge carrier mobility. In this study, we used Stille coupling polymerization to synthesize a BDT monomer with thiophene side-chains and copolymerized with dioctyl 2,5-dibromoterephthalate (DTP) to form a 2-D type donor-acceptor conjugated polymer, BDT-DTP. Thermal analyses indicated that BDT-DTP has a high thermal decomposition temperature of 342.07 °C (weight loss = 5%), showing excellent thermal stability. The active layer comprised of BDT-DTP:3,9-bis(2-methylene-(3-(1,1-dicyanomethylene)-indanone))−5,5,11,11-tetrakis(4-hexylphenyl)-dithieno[2,3-d:2′,3′-d′]-s-indaceno[1,2-b:5,6-b′]dithiophene (ITIC) blended film in a OPV device could achieve a power conversion efficiency of 1.08%, open-circuit voltage of 0.88 V, short-circuit current density of 4.08 mA cm−2, and fill factor of 30.1%. This work demonstrates a novel structure of benzodithiophene-based donor material used in the photovoltaic application.
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Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Organic Light-Emitting Diodes Research

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References (31)

Show source-provided references
1. Su · Mater. Today · 2012 · 15 · 55410.1016/S1369-7021(13)70013-0 ↗
2. Jiang · ACS Appl. Mater. Interfaces · 2021 · 13 · 107610.1021/acsami.0c19198 ↗
3. Chang · ACS Appl. Mater. Interfaces · 2020 · 12 · 5502310.1021/acsami.0c14461 ↗
4. Cheng · Nano Lett. · 2021 · 21 · 220710.1021/acs.nanolett.0c05045 ↗
5. Zhan · Energy Environ. Sci. · 2020 · 13 · 63510.1039/C9EE03710A ↗
6. Cui · Energy Environ. Sci. · 2019 · 12 · 322510.1039/C9EE02531F ↗
7. Zhang · Small Methods · 2017 · 110.1002/smtd.201700258 ↗
8. Cai · ACS Appl. Mater. Interfaces · 2020 · 12 · 5066010.1021/acsami.0c14612 ↗
9. Cheng · ACS Appl. Mater. Interfaces · 2021 · 13 · 2722710.1021/acsami.1c06762 ↗
10. Hou · J. Am. Chem. Soc. · 2006 · 128 · 491110.1021/ja060141m ↗
11. Lee · Chem. Rev. · 2019 · 119 · 802810.1021/acs.chemrev.9b00044 ↗
12. Hsu · ACS Appl. Energy Mater. · 2020 · 3 · 421710.1021/acsaem.9b02302 ↗
13. Su · J. Mater. Chem. A · 2017 · 5 · 2405110.1039/C7TA07228G ↗
14. Zhang · Sci. China Chem. · 2015 · 58 · 19210.1007/s11426-014-5260-2 ↗
15. Zhang · J. Phys. Chem. C · 2017 · 121 · 1963410.1021/acs.jpcc.7b05815 ↗
16. Zhao · J. Mater. Chem. A · 2016 · 4 · 951110.1039/C6TA03288E ↗
17. Ko · Energy Environ. Sci. · 2017 · 10 · 144310.1039/C6EE03051C ↗
18. Colladet · Macromolecules · 2007 · 40 · 6510.1021/ma061760i ↗
19. Gao · Polymers · 2017 · 9 · 3910.3390/polym9020039 ↗
20. Dou · Adv. Funct. Mater. · 2014 · 24 · 627010.1002/adfm.201401822 ↗
21. Kang · J. Am. Chem. Soc. · 2016 · 138 · 367910.1021/jacs.5b10445 ↗
22. Ye · Macromolecules · 2015 · 48 · 715610.1021/acs.macromol.5b01537 ↗
23. Yu · Chem. Eur. J. · 2020 · 26 · 1619410.1002/chem.202000220 ↗
24. Lee · Chem. Sci. · 2017 · 8 · 250310.1039/C7SC00154A ↗
25. Su · J. Phys. Chem. C · 2015 · 119 · 340810.1021/jp512315a ↗
26. Raj · J. Mater. Chem. A · 2017 · 5 · 333010.1039/C6TA09212H ↗
27. Ma · J. Mater. Chem. · 2012 · 22 · 230610.1039/C1JM14940G ↗
28. Lin · Nano Energy · 2018 · 43 · 13810.1016/j.nanoen.2017.11.016 ↗
29. Chen · Org. Electron. · 2019 · 71 · 18510.1016/j.orgel.2019.05.002 ↗
30. Luo · New J. Chem. · 2018 · 42 · 1927910.1039/C8NJ03941K ↗
31. Ibrahim · IEEE Trans. Electron Devices · 2019 · 66 · 312410.1109/TED.2019.2917594 ↗