journal article·2025-12-28Open access

Acceptor–Acceptor-Type Conjugated Polymers for Energy Level Modulation in Semiconducting Carbon Nanotube Transistors

You-Chen Chen, Megumi Matsuda, Yi-Hsuan Tung, Guo-Hao Jiang, Yu-Che Kan, Shang-Wen Su, Chien-Chung Shih, Tomoya Higashihara, Yan-Cheng Lin

Abstract

High Resolution Image Download MS PowerPoint Slide Numerous methods have been developed for sorting single-walled carbon nanotubes (SWCNTs), and polymer wrapping has become one of the most widely applied strategies for obtaining high-purity semiconducting SWCNTs (s-SWCNTs). Conjugated polymers can selectively sort s-SWCNTs, yet the role of frontier orbital level tuning in this process remains underexplored. In this study, we designed and compared four naphthalene diimide (NDI)–based copolymers with distinct backbones. Among them, the NDI-copolymers with a bithiophene donor (PNDI-2T) or a bis(thienyl)imide acceptor (PNDI-BTI) can effectively wrap onto the s-SWCNTs for investigating how modulation of the frontier energy levels affects polymer–nanotube interactions and device performance. Optical characterizations revealed that PNDI-BTI achieves s-SWCNT purity above 99%, higher than that obtained with PNDI-2T. Furthermore, PNDI-BTI exhibits stronger aggregation, leading to enhanced wrapping and the formation of longer, more uniform s-SWCNT networks, whereas PNDI-2T tends to produce more bundled structures. On the other hand, photoluminescence excitation mapping confirmed that the two polymers selectively wrap distinct nanotube chiralities, leading to noticeable differences in average tube diameter: PNDI-BTI favors large-diameter s-SWCNTs, while PNDI-2T preferentially interacts with small-diameter ones. Field-effect transistors fabricated with PNDI-BTI/s-SWCNTs show superior performance, exhibiting a high hole mobility of 2.1 cm 2 V –1 s –1 and a stably I on / I off ratio of 9 × 10 3, as well as improved endurance and bias stability, which are attributed to the lower-lying energy levels and stronger π–π interactions of PNDI-BTI. These findings demonstrate that tuning the frontier orbital levels of polymers provides an effective strategy to improve sorting selectivity and device performance, offering new insights into the design of high-performance acceptor–acceptor type conjugated polymers for s-SWCNT sorting.
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Research context

OpenAlex topics: Carbon Nanotubes in Composites · Conducting polymers and applications · Organic Electronics and Photovoltaics

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemical Engineering

National Cheng Kung University

Department of Organic Materials Science, Graduate School of Organic Materials Science, Yamagata University, 4-3-16 Jonan, Yonezawa, Yamagata 992-8510, Japan

Department of Chemical Engineering and Materials Engineering

National Yunlin University of Science and Technology

Advanced Research Center for Green Materials Science and Technology

National Taiwan University

Funding

Japan Society for the Promotion of Science · Japan Science and Technology Agency · National Science and Technology Council · Ministry of Education's Higher Education Sprout Project, Featured Area Research Center Program

References (51)

Show source-provided references
1. 10.1002/adfm.20190454510.1002/adfm.201904545 ↗
2. 10.1021/acs.chemrev.2c0069610.1021/acs.chemrev.2c00696 ↗
3. 10.1021/jacs.2c0007210.1021/jacs.2c00072 ↗
4. 10.1002/smll.20180079610.1002/smll.201800796 ↗
5. 10.1002/anie.20180751310.1002/anie.201807513 ↗
6. 10.1021/acs.chemrev.7b0000310.1021/acs.chemrev.7b00003 ↗
7. 10.1039/C6TC04269D10.1039/C6TC04269D ↗
8. 10.1002/adfm.20180183410.1002/adfm.201801834 ↗
9. 10.1021/acs.accounts.8b0001510.1021/acs.accounts.8b00015 ↗
10. 10.1021/acsami.8b0458210.1021/acsami.8b04582 ↗
11. 10.1021/acs.chemmater.0c0225810.1021/acs.chemmater.0c02258 ↗
12. 10.1021/ja806109z10.1021/ja806109z ↗
13. 10.1038/s41586-019-1493-810.1038/s41586-019-1493-8 ↗
14. 10.1021/nl050133o10.1021/nl050133o ↗
15. 10.1039/C7QM00427C10.1039/C7QM00427C ↗
16. 10.1007/s12274-011-0152-710.1007/s12274-011-0152-7 ↗
17. 10.1007/s12274-009-9057-010.1007/s12274-009-9057-0 ↗
18. 10.1143/APEX.1.11400110.1143/APEX.1.114001 ↗
19. 10.1039/c3nr05511f10.1039/c3nr05511f ↗
20. 10.1021/jz501781310.1021/jz5017813 ↗
21. 10.1002/adma.20130026710.1002/adma.201300267 ↗
22. 10.1038/nnano.2007.29010.1038/nnano.2007.290 ↗
23. 10.1021/acsami.4c0898110.1021/acsami.4c08981 ↗
24. 10.1021/nn504873410.1021/nn5048734 ↗
25. 10.1016/j.carbon.2015.07.07210.1016/j.carbon.2015.07.072 ↗
26. 10.1021/acs.macromol.0c0019310.1021/acs.macromol.0c00193 ↗
27. 10.1021/nn406256y10.1021/nn406256y ↗
28. Lee H. W. · Nat. Commun. · 2011 · 2 · 54110.1038/ncomms1545 ↗
29. 10.3390/polym1207154810.3390/polym12071548 ↗
30. 10.1002/smll.20140376110.1002/smll.201403761 ↗
31. 10.1002/aelm.20150007410.1002/aelm.201500074 ↗
32. 10.1016/j.dyepig.2014.07.01810.1016/j.dyepig.2014.07.018 ↗
33. 10.1038/s41467-022-32964-z10.1038/s41467-022-32964-z ↗
34. 10.1021/ja304198e10.1021/ja304198e ↗
35. 10.1126/science.108769110.1126/science.1087691 ↗
36. 10.1038/nmat372210.1038/nmat3722 ↗
37. 10.1021/acsnano.7b0107610.1021/acsnano.7b01076 ↗
38. 10.1021/acsnano.7b0881810.1021/acsnano.7b08818 ↗
39. 10.1016/j.physrep.2004.10.00610.1016/j.physrep.2004.10.006 ↗
40. 10.1063/5.003080910.1063/5.0030809 ↗
41. 10.1021/acssensors.0c0076410.1021/acssensors.0c00764 ↗
42. 10.1002/smll.20240365110.1002/smll.202403651 ↗
43. 10.1016/j.physrep.2004.10.00610.1016/j.physrep.2004.10.006 ↗
44. 10.1021/acs.chemrev.9b0083510.1021/acs.chemrev.9b00835 ↗
45. 10.1021/accountsmr.1c0011110.1021/accountsmr.1c00111 ↗
46. 10.1021/acs.chemmater.6b0182510.1021/acs.chemmater.6b01825 ↗
47. 10.1021/acsnano.0c0858410.1021/acsnano.0c08584 ↗
48. 10.1126/science.aba598010.1126/science.aba5980 ↗
49. 10.1039/D4NH00427B10.1039/D4NH00427B ↗
50. 10.1021/acs.macromol.1c0232910.1021/acs.macromol.1c02329 ↗
51. 10.1002/smsc.20230026810.1002/smsc.202300268 ↗