journal article·2022-02-07

Dynamics of Preaggregation and Film Formation of Donor–Acceptor π-Conjugated Polymers

Yuta Yabuuchi, Yu Minowa, Shuichi Nagamatsu, Akihiko Fujii, Masanori Ozaki

ACS Materials Letters· Volume 4· Issue 2
Publisher page

Abstract

It is important to understand the film formation mechanism of π-conjugated polymers to realize their high-performance electronic devices. In this study, the dynamics of the preaggregate, which affects the conformation and alignment of a typical donor–acceptor (D-A) π-conjugated polymer during film formation, was investigated by two approaches based on a small-angle X-ray scattering (SAXS) method. SAXS analysis of a highly concentrated solution, assuming the state before becoming the solid-state thin film, provided insight into the aggregation phenomena of the D-A π-conjugated polymer during the film formation process. In solution, the small rod-like structure of the polymer seems to form a large preaggregate, the shape of which almost coincided with that of the aggregate in the solid-state thin film. Besides, in situ grading incident SAXS (in situ GISAXS) analysis in the actual film formation process from the solution state revealed a microstructural change of the aggregate over time.
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

Graduate School of Engineering, Osaka University, 2-1 Yamada-oka, Suita, Osaka 565-0871, Japan

Department of Physics and Information Technology, Kyushu Institute of Technology, 680-4 Kawazu, Iizuka, Fukuoka 820-8502, Japan

Funding

Japan Society for the Promotion of Science · Iketani Science and Technology Foundation

References (36)

Show source-provided references
1. 10.1088/1468-6996/15/3/03420310.1088/1468-6996/15/3/034203 ↗
2. 10.1039/C9TC04397G10.1039/C9TC04397G ↗
3. 10.1038/4435910.1038/44359 ↗
4. 10.1039/C0JM02109A10.1039/C0JM02109A ↗
5. 10.1021/jp411668g10.1021/jp411668g ↗
6. 10.1039/c0cp00785d10.1039/c0cp00785d ↗
7. 10.1039/C5CP02769A10.1039/C5CP02769A ↗
8. 10.1021/nn901568w10.1021/nn901568w ↗
9. 10.1021/acs.macromol.7b0079010.1021/acs.macromol.7b00790 ↗
10. 10.7567/1347-4065/aafb5d10.7567/1347-4065/aafb5d ↗
11. 10.7567/1347-4065/ab51a810.7567/1347-4065/ab51a8 ↗
12. 10.1038/nmat161210.1038/nmat1612 ↗
13. 10.1002/adma.20120131810.1002/adma.201201318 ↗
14. 10.1002/adma.20120179510.1002/adma.201201795 ↗
15. 10.1021/acsmaterialslett.1c0032010.1021/acsmaterialslett.1c00320 ↗
16. 10.1038/srep0075410.1038/srep00754 ↗
17. 10.1002/adma.20150040110.1002/adma.201500401 ↗
18. 10.1039/D0CS00037J10.1039/D0CS00037J ↗
19. 10.1038/srep0342510.1038/srep03425 ↗
20. 10.1021/acs.chemmater.5b0377510.1021/acs.chemmater.5b03775 ↗
21. 10.1039/C5TC01425E10.1039/C5TC01425E ↗
22. 10.1021/jacs.9b1093510.1021/jacs.9b10935 ↗
23. 10.1016/j.orgel.2018.01.00610.1016/j.orgel.2018.01.006 ↗
24. 10.1002/aelm.20210031310.1002/aelm.202100313 ↗
25. 10.1002/aelm.20170055910.1002/aelm.201700559 ↗
26. 10.1021/acsami.7b0813310.1021/acsami.7b08133 ↗
27. 10.1002/adma.20150243710.1002/adma.201502437 ↗
28. 10.1126/sciadv.aaw775710.1126/sciadv.aaw7757 ↗
29. 10.1021/acsami.6b0160710.1021/acsami.6b01607 ↗
30. 10.1002/adma.20170107210.1002/adma.201701072 ↗
31. 10.1021/acs.macromol.0c0164610.1021/acs.macromol.0c01646 ↗
32. 10.1002/adma.20160237710.1002/adma.201602377 ↗
33. 10.1002/aenm.20100005410.1002/aenm.201000054 ↗
34. 10.1021/jacs.5b0049310.1021/jacs.5b00493 ↗
35. 10.1039/C8SM02517G10.1039/C8SM02517G ↗
36. Roe R.-J. · 2000