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控制可溶性聚酰亚胺栅极电介质的氟化密度及其对有机晶体生长和器件操作稳定性的影响。

Controlling Fluorination Density of Soluble Polyimide Gate Dielectrics and its Influence on Organic Crystal Growth and Device Operational Stability.

作者信息

Yoon Tae Woong, Park Hyunjin, Lee Jaehoon, Yoo Sungmi, Kim Yun Ho, Weon Byung Mook, Kim Junki, Kim Young Yong, Kang Boseok

机构信息

SKKU Advanced Institute of Nanotechnology (SAINT) and Department of Nano Science and Engineering, Sungkyunkwan University (SKKU), Suwon 16419, Republic of Korea.

Chemical Materials Solutions Center, Korea Research Institute of Chemical Technology (KRICT), Daejeon 34114, Republic of Korea.

出版信息

ACS Appl Mater Interfaces. 2024 Apr 26. doi: 10.1021/acsami.4c01767.

DOI:10.1021/acsami.4c01767
PMID:38669100
Abstract

Fluorinated polyimides (PIs) are among the most promising candidates for gate dielectric materials in organic electronic devices because of their solution processability and outstanding chemical, mechanical, and thermal stabilities. Additionally, fluorine (F) substitution improves the electrical properties of PI thin films, such as enhanced dielectric properties and reduced surface trap densities. However, the relationship between the fluorination density of PIs and crystal growth modes of vacuum-deposited conjugated molecules on PI thin films, which is directly related to the lateral charge transport along the PI-organic semiconductor interface, has not been systematically studied. Herein, five different soluble PIs with different F densities were synthesized, and the correlation between fluorination and thin-film properties was systematically investigated. Not only were their dielectric properties modulated, but the growth modes of the organic molecules deposited on the PI thin films also changed with increasing surface F density. This phenomenon was observed by both surface and crystallographic analyses, which resulted in extremely high operational stability of field-effect transistors and the successful fabrication of organic complementary circuits. We believe that the correlation between PI backbone fluorination and its thin-film properties will provide practical insights into the material design based on controlled molecular directed surface assembly on fluorinated polymer dielectrics.

摘要

氟化聚酰亚胺(PIs)因其可溶液加工性以及出色的化学、机械和热稳定性,成为有机电子器件中栅极介电材料最具潜力的候选材料之一。此外,氟(F)取代改善了PI薄膜的电学性能,如增强的介电性能和降低的表面陷阱密度。然而,PI的氟化密度与PI薄膜上真空沉积的共轭分子的晶体生长模式之间的关系尚未得到系统研究,而这一关系与沿PI - 有机半导体界面的横向电荷传输直接相关。在此,合成了五种具有不同F密度的可溶性PI,并系统地研究了氟化与薄膜性能之间的相关性。不仅调节了它们的介电性能,而且沉积在PI薄膜上的有机分子的生长模式也随着表面F密度的增加而改变。通过表面分析和晶体学分析均观察到了这一现象,这导致场效应晶体管具有极高的操作稳定性,并成功制造了有机互补电路。我们相信,PI主链氟化与其薄膜性能之间的相关性将为基于氟化聚合物电介质上可控分子定向表面组装的材料设计提供实际见解。

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