journal article·2019-04-23

A Solution Processed Ultrathin Molecular Dielectric for Organic Field-Effect Transistors

Kadaba Swathi, Vajjiravel Murugesan, Kalishankar Bhattacharyya, Titas Kumar Mukhopadhyay, Ayan Datta, Kavassery Sureswaran Narayan

Publisher page

Abstract

Leakage-free, thin molecular dielectric layers with sizable macroscopic polarization are valuable for organic field-effect transistor applications. Molecules that are designed for large polarizability tend to be accompanied by a rigid structure which limits their dynamic field response. In this context, we report a novel molecular dielectric material based on a derivative of tetrabromophthalic anhydride (TBPA). By introduction of an intramolecular twist in the molecule design, steric hindrance between neighboring polar moieties is introduced which disrupts extended ordering and leads to the formation of homogeneous, pinhole-free, amorphous and ultrathin films down to a monolayer. A high specific capacitance of the order of microfarads is observed in solution processed monolayer films which are utilized to fabricate low-voltage polymer transistors. The molecular picture shows the formation of self-assembled nanoclusters due to noncovalent intermolecular interactions which result in a macroscopic dipole moment and subsequently a high dielectric constant. The structure–property correlation is interpreted from frequency-dependent dielectric constant measurements (ε(ω)) and density functional theory studies. Subsequently, these unique properties are utilized in polymer field-effect transistors (PFET), which exhibit low leakage and turn-on at 0.6 V.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Molecular Junctions and Nanostructures · Luminescence and Fluorescent Materials

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

Affiliations

Chemistry and Physics of Materials Unit, School of Advanced Materials, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur P. O., Bangalore, India 560064

Department of Chemistry, B S Abdur Rahman Crescent Institute of Science and Technology, Vandalur, Chennai, India 600048

School of Chemical Sciences, Indian Association for the Cultivation of Science, 2A and 2B Raja S. C. Mullick Road, Jadavpur , Kolkata, West Bengal, India 700032

Funding

Indian National Science Academy · Jawaharlal Nehru Centre for Advanced Scientific Research · Department of Science and Technology, Ministry of Science and Technology · Russian Foundation for Basic Research

References (44)

Show source-provided references
1. 10.1021/ja405112s10.1021/ja405112s ↗
2. 10.1038/srep0075410.1038/srep00754 ↗
3. 10.1002/adma.20100231310.1002/adma.201002313 ↗
4. 10.1002/adfm.20090159710.1002/adfm.200901597 ↗
5. 10.1002/adma.20130117610.1002/adma.201301176 ↗
6. 10.1016/j.orgel.2014.10.00510.1016/j.orgel.2014.10.005 ↗
7. 10.1038/ncomms939410.1038/ncomms9394 ↗
8. 10.1002/polb.2214810.1002/polb.22148 ↗
9. 10.1063/1.317648010.1063/1.3176480 ↗
10. 10.1002/aelm.20157001310.1002/aelm.201570013 ↗
11. 10.1002/adma.20050115210.1002/adma.200501152 ↗
12. 10.1103/PhysRevLett.92.11680210.1103/PhysRevLett.92.116802 ↗
13. 10.1021/cm049598q10.1021/cm049598q ↗
14. 10.1002/(SICI)1521-4095(199803)10:5<365::AID-ADMA365>3.0.CO;2-U10.1002/(SICI)1521-4095(199803)10:5<365::AID-ADMA365>3.0.CO;2-U ↗
15. 10.1038/nature0553310.1038/nature05533 ↗
16. 10.1002/aelm.20150022610.1002/aelm.201500226 ↗
17. Swathi K. · 2016 · 99440T
18. 10.1021/la201161q10.1021/la201161q ↗
19. 10.1002/chem.20170257710.1002/chem.201702577 ↗
20. 10.1021/jacs.5b0041210.1021/jacs.5b00412 ↗
21. 10.1021/jacs.5b0330110.1021/jacs.5b03301 ↗
22. Wright J. D. · 1995
23. 10.1021/acs.accounts.6b0017310.1021/acs.accounts.6b00173 ↗
24. 10.1021/acs.chemrev.7b0008410.1021/acs.chemrev.7b00084 ↗
25. 10.1002/aenm.20180375510.1002/aenm.201803755 ↗
26. 10.1103/PhysRev.95.35910.1103/PhysRev.95.359 ↗
27. 10.1038/nature0298710.1038/nature02987 ↗
28. 10.1007/BF0053348510.1007/BF00533485 ↗
29. Frisch, M. J.; Trucks, G.; Schlegel, H. B.; Scuseria, G.; Robb, M.; Cheeseman, J.; Scalmani, G.; Barone, V.; Mennucci, B.; Petersson, G. Gaussian 09, Revision A.1; Gaussian Inc.:Wallingford, CT, 2009; Vol. 27, p 34.
30. 10.1021/jz400263y10.1021/jz400263y ↗
31. 10.1021/ja100936w10.1021/ja100936w ↗
32. 10.1021/ct100641a10.1021/ct100641a ↗
33. 10.1021/acs.inorgchem.6b0191110.1021/acs.inorgchem.6b01911 ↗
34. 10.1021/jp070186p10.1021/jp070186p ↗
35. 10.1021/ct300849w10.1021/ct300849w ↗
36. 10.1021/ct100684s10.1021/ct100684s ↗
37. 10.1016/j.eurpolymj.2011.02.01610.1016/j.eurpolymj.2011.02.016 ↗
38. 10.1063/1.341396110.1063/1.3413961 ↗
39. 10.1002/andp.1912344140410.1002/andp.19123441404 ↗
40. 10.1088/0022-3727/32/14/20110.1088/0022-3727/32/14/201 ↗
41. 10.1021/acsami.6b0948010.1021/acsami.6b09480 ↗
42. 10.1103/PhysRevB.91.11530210.1103/PhysRevB.91.115302 ↗
43. 10.1021/ja308211n10.1021/ja308211n ↗
44. Sze S. M. · 200610.1002/0470068329 ↗