journal article·2014-06

Effect of Non‐Chlorinated Mixed Solvents on Charge Transport and Morphology of Solution‐Processed Polymer Field‐Effect Transistors

Wen‐Ya Lee, Gaurav Giri, Ying Diao, Christopher J. Tassone, James R. Matthews, Michael L. Sorensen, Stefan C. B. Mannsfeld, Wen‐Chang Chen, Hon H. Fong, Jeffrey B.‐H. Tok, Michael F. Toney, Mingqian He, Zhenan Bao

Advanced Functional Materials· Volume 24· Issue 23
Publisher page

Abstract

Using non‐chlorinated solvents for polymer device fabrication is highly desirable to avoid the negative environmental and health effects of chlorinated solvents. Here, a non‐chlorinated mixed solvent system, composed by a mixture of tetrahydronaphthalene and p­‐xylene, is described for processing a high mobility donor‐acceptor fused thiophene‐diketopyrrolopyrrole copolymer (PTDPPTFT4) in thin film transistors. The effects of the use of a mixed solvent system on the device performance, e.g., charge transport, morphology, and molecular packing, are investigated. p‐Xylene is chosen to promote polymer aggregation in solution, while a higher boiling point solvent, tetrahydronaphthalene, is used to allow a longer evaporation time and better solubility, which further facilitates morphological tuning. By optimizing the ratio of the two solvents, the charge transport characteristics of the polymer semiconductor device are observed to significantly improve for polymer devices deposited by spin coating and solution shearing. Average charge carrier mobilities of 3.13 cm2 V−1 s−1 and a maximum value as high as 3.94 cm2 V−1 s−1 are obtained by solution shearing. The combination of non‐chlorinated mixed solvents and the solution shearing film deposition provide a practical and environmentally‐friendly approach to achieve high performance polymer transistor devices.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Advanced Memory and Neural Computing · Semiconductor materials and devices

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

Affiliations

Department of Chemical Engineering Stanford University 381 North‐South Mall Stanford CA 94305 USA

Stanford Synchrotron Radiation Laboratory 2575 Sand Hill Rd Menlo Park CA 94025 USA

Corning Incorporated SP‐FR‐06–1 Corning NY 14831 USA

Department of Chemical Engineering National Taiwan University Taipei 106 Taiwan

Shanghai Jiao Tong University, Comprehensive Laboratory Building Room 2–603, 800 DongChuan Rd. Shanghai 200240 China

Funding

National Science Foundation DMR Solid State Chemistry · Corning Corporation · National Science Council, Taiwan · Department of Energy, Laboratory Directed Research and Development funding

References (55)

Show source-provided references
1. 10.1021/cr050154310.1021/cr0501543 ↗
2. 10.1201/978142000801210.1201/9781420008012 ↗
3. 10.1021/cr900150b10.1021/cr900150b ↗
4. 10.1063/1.11783410.1063/1.117834 ↗
5. 10.1002/adma.20080272210.1002/adma.200802722 ↗
6. 10.1063/1.282484510.1063/1.2824845 ↗
7. 10.1021/ja108861q10.1021/ja108861q ↗
8. 10.1002/adma.20110305710.1002/adma.201103057 ↗
9. 10.1021/ja209328m10.1021/ja209328m ↗
10. 10.1021/ja310283f10.1021/ja310283f ↗
11. 10.1002/adma.20100231310.1002/adma.201002313 ↗
12. 10.1038/srep0075410.1038/srep00754 ↗
13. 10.1039/C1JM14640H10.1039/C1JM14640H ↗
14. 10.1002/adma.20120286710.1002/adma.201202867 ↗
15. 10.1021/cm302341m10.1021/cm302341m ↗
16. 10.1021/ja308211n10.1021/ja308211n ↗
17. 10.1021/ja308927g10.1021/ja308927g ↗
18. 10.1002/adma.20129020410.1002/adma.201290204 ↗
19. 10.1021/ja203189h10.1021/ja203189h ↗
20. 10.1021/ja110619k10.1021/ja110619k ↗
21. 10.1021/ja104932410.1021/ja1049324 ↗
22. 10.1021/cm049617w10.1021/cm049617w ↗
23. 10.1002/adfm.20040029710.1002/adfm.200400297 ↗
24. 10.1002/adfm.20080176310.1002/adfm.200801763 ↗
25. 10.1021/cm900628j10.1021/cm900628j ↗
26. 10.1021/ja210430b10.1021/ja210430b ↗
27. 10.1002/adma.20120015110.1002/adma.201200151 ↗
28. 10.1002/adma.20137006210.1002/adma.201370062 ↗
29. 10.1002/adma.20040117110.1002/adma.200401171 ↗
30. 10.1002/adma.20070312010.1002/adma.200703120 ↗
31. 10.1038/nature1068310.1038/nature10683 ↗
32. 10.1002/adfm.20110160610.1002/adfm.201101606 ↗
33. 10.1021/ja110486s10.1021/ja110486s ↗
34. 10.1002/adfm.20120094010.1002/adfm.201200940 ↗
35. 10.1038/nmat365010.1038/nmat3650 ↗
36. 10.1021/cm303953e10.1021/cm303953e ↗
37. 10.1021/ma900544510.1021/ma9005445 ↗
38. 10.1002/macp.20110028410.1002/macp.201100284 ↗
39. 10.1002/aenm.20100005410.1002/aenm.201000054 ↗
40. 10.1002/adfm.20080172710.1002/adfm.200801727 ↗
41. 10.1021/ja902995710.1021/ja9029957 ↗
42. 10.1039/B819210C10.1039/B819210C ↗
43. 10.1038/nmat365010.1038/nmat3650 ↗
44. 10.1107/S002188981001577310.1107/S0021889810015773 ↗
45. 10.1107/S002188989501160510.1107/S0021889895011605 ↗
46. 10.1107/S002188989500529210.1107/S0021889895005292 ↗
47. 10.1063/1.306006910.1063/1.3060069 ↗
48. Roe R.‐J. · 2000
49. Flory P. J. · 1953
50. 10.1021/ma070900110.1021/ma0709001 ↗
51. 10.1021/cr300110910.1021/cr3001109 ↗
52. 10.1002/adfm.20120240810.1002/adfm.201202408 ↗
53. 10.1002/adma.20100313510.1002/adma.201003135 ↗
54. 10.1021/cm900637p10.1021/cm900637p ↗
55. 10.1063/1.313390210.1063/1.3133902 ↗