A new ambipolar copolymer for organic electronics
Source abstract
Abstract
The 5-(heptadecan-9-yl)dithieno[3,2-b:2′,3′-d]pyridine (NET) structure was designed as a new donor unit for copolymer synthesis. Benzothiadiazole (BT) was used as the electron acceptor unit. The new donor–acceptor copolymer was obtained through the Stille coupling reaction. The density functional theory analysis of the new copolymer showed that the highest occupied molecular orbital electron density was localized on the NET unit while the lowest unoccupied molecular orbital electron density was localized partially on the BT and partially on the pyridine group of the NET unit. The polymer presented good solubility and thermal stability, which are desirable properties for use in solution-processed devices. The new polymer is expected to show a potential for application in organic electronics, such as thin-film transistors.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Organic Light-Emitting Diodes Research · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Materials Science and Engineering and Research Institute for Green Energy Convergence Technology (RIGET), Gyeongsang National University, Jin-ju, Republic of Korea
Department of Materials Engineering, Convergence Technology and Institute for Green Energy Convergence Technology (RIGET), Gyeongsang National University, Jin-ju, Republic of Korea
Funding
National Research Foundation of Korea (NRF)
References (20)
Show source-provided references
1. 10.1063/1.494688810.1063/1.4946888 ↗
2. 10.1002/adma.20090405410.1002/adma.200904054 ↗
3. 10.1002/bkcs.1039710.1002/bkcs.10397 ↗
4. 10.1021/acsami.6b0185210.1021/acsami.6b01852 ↗
5. 10.1166/jnn.2015.932410.1166/jnn.2015.9324 ↗
6. 10.1016/j.orgel.2016.04.02710.1016/j.orgel.2016.04.027 ↗
7. 10.1002/adma.20120286710.1002/adma.201202867 ↗
8. 10.1021/acs.chemmater.6b0474510.1021/acs.chemmater.6b04745 ↗
9. 10.1016/j.matchemphys.2014.12.03510.1016/j.matchemphys.2014.12.035 ↗
10. 10.1007/s11426-015-0511-910.1007/s11426-015-0511-9 ↗
11. 10.1166/jnn.2014.880510.1166/jnn.2014.8805 ↗
12. 10.1016/j.orgel.2016.03.03410.1016/j.orgel.2016.03.034 ↗
13. 10.1039/c6ra03221d10.1039/c6ra03221d ↗
14. 10.1063/1.494314010.1063/1.4943140 ↗
15. 10.1016/j.snb.2015.12.05610.1016/j.snb.2015.12.056 ↗
16. 10.1016/j.orgel.2016.02.01310.1016/j.orgel.2016.02.013 ↗
17. 10.1166/jnn.2014.880410.1166/jnn.2014.8804 ↗
18. 10.1016/j.orgel.2017.08.02310.1016/j.orgel.2017.08.023 ↗
19. 10.1166/jnn.2017.1312010.1166/jnn.2017.13120 ↗
20. 10.1021/ma400452j10.1021/ma400452j ↗