journal article·2022-08

Highly Efficient Mixed Conduction in N‐type Fused Small Molecule Semiconductors

Jiayao Duan, Genming Zhu, Lewen Wang, Junxin Chen, Shengyu Cong, Xiuyuan Zhu, Yecheng Zhou, Zhengke Li, Iain McCulloch, Wan Yue

Advanced Functional Materials· Volume 32· Issue 34
Publisher page

Abstract

Abstract Highly efficient mixed ionic and electronic conduction is critical to developing high‐performance organic electrochemical transistors (OECTs) devices. While currently, the n‐type small molecules mixed conductors design strategy remains extremely lacking. Herein, ethylene glycol (EG) chain substituted electron‐deficient naphthalene bis‐isatin and rhodanine acceptor units with easily accessible steps are rationally fused, affording fused and planar novel semiconductors with weak intramolecular S–O ‘conformation locks', where gNR with EG side chain and hgNR with hybrid alkyl‐EG side chain. The rigid, planar and highly electron‐deficient skeleton enables the resulting small molecule semiconductors to be efficient mixed ionic‐electronic conductors with very high OECT electron mobility up to 0.01 cm2 V−1 s−1. Remarkedly, gNR displays the record value of geometry‐normalized transconductance of 0.4 S cm−1 and μC* of 2.6 F V−1 cm−1 s−1, which can also be compared with the state‐of‐art n‐type semiconducting polymers in OECTs. Moreover, the effect of the alkyl spacer on the n‐type mixed ionic and electronic conduction features of the small molecule materials is investigated. The fused electron‐deficient acceptor‐acceptor (A–A) system with intramolecular conformation lock design strategy in this work provides a new avenue to realize next‐generation high‐performance small molecule mixed ionic and electronic conductors for OECT materials.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Conducting polymers and applications · Organic Electronics and Photovoltaics · Perovskite Materials and Applications

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

Affiliations

Guangzhou Key Laboratory of Flexible Electronic Materials and Wearable Devices School of Materials and Engineering Sun Yat‐Sen University Guangzhou 510275 China

Department of Chemistry Chemistry Research Laboratory University of Oxford Oxford OX1 3TA UK

Funding

National Natural Science Foundation of China

References (68)

Show source-provided references
1. 10.1038/natrevmats.2017.8610.1038/natrevmats.2017.86 ↗
2. 10.1002/adma.20180094110.1002/adma.201800941 ↗
3. 10.1038/s41563-019-0435-z10.1038/s41563-019-0435-z ↗
4. 10.1002/adfm.20180703310.1002/adfm.201807033 ↗
5. 10.1021/acs.accounts.8b0044810.1021/acs.accounts.8b00448 ↗
6. 10.1002/adma.20210187410.1002/adma.202101874 ↗
7. 10.3390/molecules2522528810.3390/molecules25225288 ↗
8. 10.1002/adma.20200143910.1002/adma.202001439 ↗
9. 10.1002/adfm.20060123910.1002/adfm.200601239 ↗
10. 10.1073/pnas.110706310810.1073/pnas.1107063108 ↗
11. 10.1126/sciadv.140025110.1126/sciadv.1400251 ↗
12. 10.1021/acsmacrolett.0c0003710.1021/acsmacrolett.0c00037 ↗
13. 10.1039/D1ME00134E10.1039/D1ME00134E ↗
14. 10.1021/jacs.6b0528010.1021/jacs.6b05280 ↗
15. 10.1021/acs.chemrev.1c0026610.1021/acs.chemrev.1c00266 ↗
16. 10.1002/pol.2021050310.1002/pol.20210503 ↗
17. 10.1039/D1TC02048J10.1039/D1TC02048J ↗
18. 10.1021/jacs.1c0351610.1021/jacs.1c03516 ↗
19. 10.1021/acs.chemmater.1c0379710.1021/acs.chemmater.1c03797 ↗
20. 10.1002/adma.20200274810.1002/adma.202002748 ↗
21. 10.1039/D1MH01889B10.1039/D1MH01889B ↗
22. 10.1002/adma.20210623510.1002/adma.202106235 ↗
23. 10.1002/anie.20210928110.1002/anie.202109281 ↗
24. 10.1002/adfm.20211143910.1002/adfm.202111439 ↗
25. 10.1002/adfm.20211195010.1002/adfm.202111950 ↗
26. 10.1002/adfm.20200871810.1002/adfm.202008718 ↗
27. 10.1038/s41563-019-0556-410.1038/s41563-019-0556-4 ↗
28. 10.1039/D0MH00548G10.1039/D0MH00548G ↗
29. 10.1039/C7TC01680H10.1039/C7TC01680H ↗
30. 10.1126/sciadv.aaz063210.1126/sciadv.aaz0632 ↗
31. 10.1021/acs.chemrev.1c0031410.1021/acs.chemrev.1c00314 ↗
32. 10.1002/aelm.20200021510.1002/aelm.202000215 ↗
33. 10.1021/acsami.9b1137010.1021/acsami.9b11370 ↗
34. 10.1021/acsami.1c2426710.1021/acsami.1c24267 ↗
35. 10.1126/sciadv.abe528010.1126/sciadv.abe5280 ↗
36. 10.1002/adma.20200006310.1002/adma.202000063 ↗
37. 10.1038/s41467-018-02852-610.1038/s41467-018-02852-6 ↗
38. 10.1021/acs.accounts.0c0048010.1021/acs.accounts.0c00480 ↗
39. 10.1002/adfm.20201016510.1002/adfm.202010165 ↗
40. 10.1002/anie.20201399810.1002/anie.202013998 ↗
41. 10.1039/C9TC02021G10.1039/C9TC02021G ↗
42. 10.1002/adfm.20201097910.1002/adfm.202010979 ↗
43. 10.1021/acs.macromol.1c0174010.1021/acs.macromol.1c01740 ↗
44. 10.1002/anie.20211307810.1002/anie.202113078 ↗
45. 10.1039/D0TC03347B10.1039/D0TC03347B ↗
46. 10.1007/s40843-019-9465-410.1007/s40843-019-9465-4 ↗
47. 10.1002/aenm.20110057210.1002/aenm.201100572 ↗
48. 10.1021/acsami.6b1571710.1021/acsami.6b15717 ↗
49. 10.1021/acsami.9b0428410.1021/acsami.9b04284 ↗
50. 10.1021/acs.chemrev.7b0008410.1021/acs.chemrev.7b00084 ↗
51. 10.1021/jp304009g10.1021/jp304009g ↗
52. 10.1039/D0SC06583H10.1039/D0SC06583H ↗
53. 10.1039/C8ME00093J10.1039/C8ME00093J ↗
54. 10.1038/ncomms270710.1038/ncomms2707 ↗
55. 10.1002/asia.20190014210.1002/asia.201900142 ↗
56. 10.1021/jacs.9b0964010.1021/jacs.9b09640 ↗
57. 10.1016/0584-8539(88)80091-610.1016/0584-8539(88)80091-6 ↗
58. 10.1021/ma990567410.1021/ma9905674 ↗
59. 10.1021/acsapm.8b0006110.1021/acsapm.8b00061 ↗
60. 10.1038/ncomms1306610.1038/ncomms13066 ↗
61. 10.1016/j.snb.2007.05.04610.1016/j.snb.2007.05.046 ↗
62. 10.1021/acsami.0c1859910.1021/acsami.0c18599 ↗
63. 10.1021/jacs.1c0671310.1021/jacs.1c06713 ↗
64. 10.1038/s41467-018-06084-610.1038/s41467-018-06084-6 ↗
65. 10.1021/acs.chemmater.5b0334910.1021/acs.chemmater.5b03349 ↗
66. 10.1021/jacs.2c0073510.1021/jacs.2c00735 ↗
67. 10.1002/anie.20210608410.1002/anie.202106084 ↗
68. 10.1002/adma.20210782910.1002/adma.202107829 ↗