journal article·2022-09-28

Fluorinated Alcohol-Processed N-Type Organic Electrochemical Transistor with High Performance and Enhanced Stability

Genming Zhu, Junxin Chen, Jiayao Duan, Hailiang Liao, Xiuyuan Zhu, Zhengke Li, Iain McCulloch, Wan Yue

ACS Applied Materials & Interfaces· Volume 14· Issue 38
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Abstract

Tuning the film morphology and aggregated structure is a vital means to improve the performance of the mixed ionic–electronic conductors in organic electrochemical transistors (OECTs). Herein, three fluorinated alcohols (FAs), including 2,2,2-trifluoroethanol (TFE), 1,1,1,3,3,3-hexafluoroisopropanol (HFIP), and perfluoro-tert-butanol (PFTB), were employed as the alternative solvents for engineering the n-type small-molecule active layer gNR. Remarkedly, an impressive μC* of 5.12 F V–1 cm–1 s–1 and a normalized transconductance of 1.216 S cm–1 are achieved from the HFIP-fabricated gNR OECTs, which is three times higher than that of chloroform. The operational stability has been significantly enhanced by the FA-fabricated devices. Such enhancements can be ascribed to the aggregation-induced structural ordering by FAs during spin coating, which optimizes the microstructure of the films for a better mixed ion and electron transport. These results prove the huge research potential of FAs to improve OECT materials’ processability, device performance, and stability, therefore promoting practical bio-applications.
Source: openalex_inverted_index · 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, State Key Laboratory of Optoelectronic Materials and Technologies, 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 (67)

Show source-provided references
1. 10.1038/natrevmats.2017.8610.1038/natrevmats.2017.86 ↗
2. 10.1002/adma.20110201710.1002/adma.201102017 ↗
3. 10.1002/adfm.20060124110.1002/adfm.200601241 ↗
4. 10.1002/adfm.20200720510.1002/adfm.202007205 ↗
5. 10.1038/nmat485610.1038/nmat4856 ↗
6. 10.1002/adhm.20140035610.1002/adhm.201400356 ↗
7. 10.1002/adfm.20190698210.1002/adfm.201906982 ↗
8. 10.1126/sciadv.aau737810.1126/sciadv.aau7378 ↗
9. 10.1021/jacs.1c0351610.1021/jacs.1c03516 ↗
10. 10.1002/adma.20200274810.1002/adma.202002748 ↗
11. 10.1126/sciadv.aat091110.1126/sciadv.aat0911 ↗
12. 10.1038/ncomms509710.1038/ncomms5097 ↗
13. 10.1039/C8TC03185A10.1039/C8TC03185A ↗
14. 10.1002/adma.20130434610.1002/adma.201304346 ↗
15. 10.1021/acsami.9b2160410.1021/acsami.9b21604 ↗
16. 10.1021/acs.chemrev.1c0031410.1021/acs.chemrev.1c00314 ↗
17. 10.1039/c2cs15313k10.1039/c2cs15313k ↗
18. 10.1021/acsami.9b1137010.1021/acsami.9b11370 ↗
19. 10.1021/acsami.1c2426710.1021/acsami.1c24267 ↗
20. 10.1002/adfm.20220393710.1002/adfm.202203937 ↗
21. 10.1039/D1TC00440A10.1039/D1TC00440A ↗
22. 10.1016/j.orgel.2013.11.00410.1016/j.orgel.2013.11.004 ↗
23. 10.1038/s41467-020-16648-010.1038/s41467-020-16648-0 ↗
24. 10.1021/acs.chemmater.8b0032110.1021/acs.chemmater.8b00321 ↗
25. 10.1021/jacs.6b0528010.1021/jacs.6b05280 ↗
26. 10.1002/adfm.20201016510.1002/adfm.202010165 ↗
27. 10.1039/D1ME00134E10.1039/D1ME00134E ↗
28. 10.1002/adma.20170711410.1002/adma.201707114 ↗
29. 10.1021/ja710079w10.1021/ja710079w ↗
30. 10.1063/1.355387810.1063/1.3553878 ↗
31. 10.1002/aelm.20190024910.1002/aelm.201900249 ↗
32. Lingstedt L. V. · Adv. Electron. Mater. · 2019 · 5 · 180080410.1002/aelm.201800804 ↗
33. 10.1039/c3ee41838c10.1039/c3ee41838c ↗
34. 10.1002/adma.20170397310.1002/adma.201703973 ↗
35. 10.1002/adsc.20150050010.1002/adsc.201500500 ↗
36. 10.1002/tcr.20190002010.1002/tcr.201900020 ↗
37. 10.1002/adfm.20211195010.1002/adfm.202111950 ↗
38. 10.1016/j.orgel.2017.10.02810.1016/j.orgel.2017.10.028 ↗
39. 10.1021/ja054546310.1021/ja0545463 ↗
40. 10.1002/adma.20220134010.1002/adma.202201340 ↗
41. 10.1002/adma.20190344110.1002/adma.201903441 ↗
42. 10.1146/annurev-physchem-040513-10363910.1146/annurev-physchem-040513-103639 ↗
43. 10.1002/aenm.20110057210.1002/aenm.201100572 ↗
44. 10.1021/jacs.6b0104610.1021/jacs.6b01046 ↗
45. 10.1021/ja903636q10.1021/ja903636q ↗
46. 10.1016/j.jphotochem.2009.02.01810.1016/j.jphotochem.2009.02.018 ↗
47. 10.1016/j.tsf.2007.04.14910.1016/j.tsf.2007.04.149 ↗
48. 10.1002/adma.20110397810.1002/adma.201103978 ↗
49. 10.1021/acs.chemmater.9b0379810.1021/acs.chemmater.9b03798 ↗
50. 10.1021/acs.jpcc.2c0215510.1021/acs.jpcc.2c02155 ↗
51. Szumska A. A. · J. Am. Chem. Soc. · 2021 · 143 · 1479510.1021/jacs.1c06713 ↗
52. 10.1021/acs.accounts.9b0015910.1021/acs.accounts.9b00159 ↗
53. 10.1021/acssensors.1c0194210.1021/acssensors.1c01942 ↗
54. 10.1002/solr.20180023010.1002/solr.201800230 ↗
55. 10.1002/adma.20200704110.1002/adma.202007041 ↗
56. 10.1002/adfm.20190765710.1002/adfm.201907657 ↗
57. 10.1021/acsami.0c1156110.1021/acsami.0c11561 ↗
58. 10.1039/D1CE01536B10.1039/D1CE01536B ↗
59. 10.1002/anie.20191048910.1002/anie.201910489 ↗
60. 10.1021/jacs.1c1065110.1021/jacs.1c10651 ↗
61. 10.1002/adma.20170548510.1002/adma.201705485 ↗
62. 10.1039/D1EE01310F10.1039/D1EE01310F ↗
63. 10.1002/adfm.20130357110.1002/adfm.201303571 ↗
64. 10.1038/nature1068310.1038/nature10683 ↗
65. 10.1021/acs.jpclett.7b0280810.1021/acs.jpclett.7b02808 ↗
66. 10.1002/ange.20030173910.1002/ange.200301739 ↗
67. 10.1055/s-2003-4497310.1055/s-2003-44973 ↗