Enhancing Thermoelectric Performance of Polyaniline/Single-Walled Carbon Nanotube Composites via Dimethyl Sulfoxide-Mediated Electropolymerization
Source abstract
Abstract
The fabrication of flexible high-performance organic/inorganic thermoelectric (TE) composite films has been a hot spot for researchers in recent years. In this work, dynamic 3-phase interfacial electropolymerization of aniline, together with physical mixing with single-walled carbon nanotubes (SWCNTs), was adopted to prepare polyaniline/SWCNT (PANI/SWCNT) TE composites. The dimethyl sulfoxide (DMSO) added into the electrochemical polymerization system affords strong capability in improving the TE performance of composite films. Moreover, varying loadings of SWCNTs can also conveniently tune the TE performance of composites. Hence, the resultant composites afford the highest power factor (PF) of 236.4 ± 5.9 μW m–1 K–2 at room temperature. This work demonstrates that the introduction of DMSO into the electrolyte and the electrochemical polymerization are highly effective in fabricating high-performance PANI/SWCNT TE composites.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Thermoelectric Materials and Devices · Conducting polymers and applications · Advanced Battery Materials and Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemical Sciences, University of Chinese Academy of Sciences, Beijing 100049, P. R. China
School of Chemical Engineering, University of Chinese Academy of Sciences, Beijing 100049, P. R. China
Funding
National Natural Science Foundation of China
References (39)
Show source-provided references
1. 10.1016/j.compscitech.2016.01.01410.1016/j.compscitech.2016.01.014 ↗
2. 10.1039/c8tc01900b10.1039/c8tc01900b ↗
3. 10.1039/c8qi00366a10.1039/c8qi00366a ↗
4. 10.3390/polym1101010710.3390/polym11010107 ↗
5. 10.1002/adma.20130537110.1002/adma.201305371 ↗
6. 10.1039/c9ta11717b10.1039/c9ta11717b ↗
7. 10.1021/acs.macromol.9b0245310.1021/acs.macromol.9b02453 ↗
8. 10.1016/j.synthmet.2020.11631810.1016/j.synthmet.2020.116318 ↗
9. 10.1016/j.carbon.2019.03.08810.1016/j.carbon.2019.03.088 ↗
10. 10.1021/acsami.9b1794710.1021/acsami.9b17947 ↗
11. 10.1002/adfm.20190559010.1002/adfm.201905590 ↗
12. 10.1016/j.orgel.2019.03.00610.1016/j.orgel.2019.03.006 ↗
13. 10.1016/j.carbon.2018.04.08310.1016/j.carbon.2018.04.083 ↗
14. 10.1021/acsami.7b0838210.1021/acsami.7b08382 ↗
15. 10.1016/j.apsusc.2019.06.24910.1016/j.apsusc.2019.06.249 ↗
16. 10.1016/j.compscitech.2019.10779410.1016/j.compscitech.2019.107794 ↗
17. 10.1016/j.synthmet.2018.11.01610.1016/j.synthmet.2018.11.016 ↗
18. 10.1039/c4tc02471k10.1039/c4tc02471k ↗
19. 10.1002/anie.20190110610.1002/anie.201901106 ↗
20. 10.1039/c9tc05710b10.1039/c9tc05710b ↗
21. 10.1016/j.orgel.2016.09.00810.1016/j.orgel.2016.09.008 ↗
22. 10.1016/j.compscitech.2019.10776710.1016/j.compscitech.2019.107767 ↗
23. 10.1002/er.553510.1002/er.5535 ↗
24. 10.1002/adma.20090222110.1002/adma.200902221 ↗
25. 10.1039/c4ee01905a10.1039/c4ee01905a ↗
26. 10.1039/c7cp07896j10.1039/c7cp07896j ↗
27. 10.1021/acsami.6b1532710.1021/acsami.6b15327 ↗
28. 10.1039/c8ta04838j10.1039/c8ta04838j ↗
29. 10.1016/j.carbon.2019.04.00710.1016/j.carbon.2019.04.007 ↗
30. 10.1039/c3ta14960a10.1039/c3ta14960a ↗
31. 10.1039/c4ta01541j10.1039/c4ta01541j ↗
32. 10.1021/nn100256210.1021/nn1002562 ↗
33. 10.1016/j.orgel.2017.09.03010.1016/j.orgel.2017.09.030 ↗
34. 10.1088/0957-4484/24/21/21570310.1088/0957-4484/24/21/215703 ↗
35. 10.1016/j.compositesb.2012.02.02810.1016/j.compositesb.2012.02.028 ↗
36. 10.1039/c2jm32750c10.1039/c2jm32750c ↗
37. 10.1177/095400831453808110.1177/0954008314538081 ↗
38. 10.1039/b104009j10.1039/b104009j ↗
39. 10.1016/j.compscitech.2020.10802310.1016/j.compscitech.2020.108023 ↗