High Tg Cyclic Olefin Copolymer Gate Dielectrics for N,N′‐Ditridecyl Perylene Diimide Based Field‐Effect Transistors: Improving Performance and Stability with Thermal Treatment
Source abstract
Abstract
Abstract A novel application of ethylene‐norbornene cyclic olefin copolymers (COC) as gate dielectric layers in organic field‐effect transistors (OFETs) that require thermal annealing as a strategy for improving the OFET performance and stability is reported. The thermally‐treated N,N′‐ditridecyl perylene diimide (PTCDI‐C13)‐based n‐type FETs using a COC/SiO2 gate dielectric show remarkably enhanced atmospheric performance and stability. The COC gate dielectric layer displays a hydrophobic surface (water contact angle = 95° ± 1°) and high thermal stability (glass transition temperature = 181 °C) without producing crosslinking. After thermal annealing, the crystallinity improves and the grain size of PTCDI‐C13 domains grown on the COC/SiO2 gate dielectric increases significantly. The resulting n‐type FETs exhibit high atmospheric field‐effect mobilities, up to 0.90 cm2 V−1 s−1 in the 20 V saturation regime and long‐term stability with respect to H2O/O2 degradation, hysteresis, or sweep‐stress over 110 days. By integrating the n‐type FETs with p‐type pentacene‐based FETs in a single device, high performance organic complementary inverters that exhibit high gain (exceeding 45 in ambient air) are realized.
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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.
References (40)
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1. 10.1002/1521-4095(20020116)14:2<99::AID-ADMA99>3.0.CO;2-910.1002/1521-4095(20020116)14:2<99::AID-ADMA99>3.0.CO;2-9 ↗
2. 10.1002/adma.20080273310.1002/adma.200802733 ↗
3. 10.1063/1.157955410.1063/1.1579554 ↗
4. 10.1038/nature0249810.1038/nature02498 ↗
5. 10.1073/pnas.040191810110.1073/pnas.0401918101 ↗
6. 10.1002/adfm.20080115510.1002/adfm.200801155 ↗
7. 10.1063/1.307719210.1063/1.3077192 ↗
8. 10.1038/nature0553310.1038/nature05533 ↗
9. 10.1002/adma.20080062910.1002/adma.200800629 ↗
10. 10.1021/cm049391x10.1021/cm049391x ↗
11. 10.1002/anie.20046132410.1002/anie.200461324 ↗
12. 10.1038/3500660310.1038/35006603 ↗
13. 10.1021/ja972762910.1021/ja9727629 ↗
14. 10.1021/ja901077a10.1021/ja901077a ↗
15. 10.1002/adma.20080320710.1002/adma.200803207 ↗
16. 10.1002/adma.20080293410.1002/adma.200802934 ↗
17. 10.1063/1.298042110.1063/1.2980421 ↗
18. 10.1038/nature0337610.1038/nature03376 ↗
19. 10.1021/nl071495u10.1021/nl071495u ↗
20. 10.1063/1.234929010.1063/1.2349290 ↗
21. 10.1002/pssr.20070126710.1002/pssr.200701267 ↗
22. 10.1063/1.219959210.1063/1.2199592 ↗
23. 10.1063/1.242466610.1063/1.2424666 ↗
24. 10.1021/ma971041r10.1021/ma971041r ↗
25. 10.1002/anie.20046197110.1002/anie.200461971 ↗
26. 10.1021/ie030412r10.1021/ie030412r ↗
27. 10.1103/PhysRevE.56.570510.1103/PhysRevE.56.5705 ↗
28. 10.1126/science.114645810.1126/science.1146458 ↗
29. 10.1063/1.217685810.1063/1.2176858 ↗
30. 10.1103/PhysRevB.70.12540110.1103/PhysRevB.70.125401 ↗
31. 10.1063/1.214605910.1063/1.2146059 ↗
32. 10.1063/1.289085310.1063/1.2890853 ↗
33. 10.1063/1.290797410.1063/1.2907974 ↗
34. 10.1063/1.195490110.1063/1.1954901 ↗
35. 10.1063/1.274338610.1063/1.2743386 ↗
36. 10.1002/adma.20090027710.1002/adma.200900277 ↗
37. 10.1021/ja052478e10.1021/ja052478e ↗
38. 10.1063/1.269587310.1063/1.2695873 ↗
39. 10.1038/nature0772710.1038/nature07727 ↗
40. 10.1007/978-94-015-7764-9_210.1007/978-94-015-7764-9_2 ↗