| Literature DB >> 28736833 |
Jie Yang1,2, Zhiyuan Zhao2, Hua Geng3, Changli Cheng4, Jinyang Chen2, Yunlong Sun2, Longxian Shi2, Yuanping Yi2, Zhigang Shuai4, Yunlong Guo2, Shuai Wang1, Yunqi Liu2.
Abstract
So far, most of the reported high-mobility conjugated polymers are p-type semiconductors. By contrast, the advances in high-mobility ambipolar polymers fall greatly behind those of p-type counterparts. Instead of unipolar p-type and n-type materials, ambipolar polymers, especially balanced ambipolar polymers, are potentially serviceable for easy-fabrication and low-cost complementary metal-oxide-semiconductor circuits. Therefore, it is a critical issue to develop high-mobility ambipolar polymers. Here, three isoindigo-based polymers, PIID-2FBT, P1FIID-2FBT, and P2FIID-2FBT are developed for high-performance ambipolar organic field-effect transistors. After the incorporation of fluorine atoms, the polymers exhibit enhanced coplanarity, lower energy levels, higher crystallinity, and thus increased µe . P2FIID-2FBT exhibits n-type dominant performance with a µe of 9.70 cm2 V-1 s-1 . Moreover, P1FIID-2FBT exhibits a highly balanced µh and µe of 6.41 and 6.76 cm2 V-1 s-1 , respectively, which are among the highest values for balanced ambipolar polymers. Moreover, a concept "effective mass" is introduced to further study the reasons for the high performance of the polymers. All the polymers have small effective masses, indicating good intramolecular charge transport. The results demonstrate that high-mobility ambipolar semiconductors can be obtained by designing polymers with fine-tuned energy levels, small effective masses, and high crystallinity.Entities:
Keywords: ambipolar; effective mass; field-effect transistors; fluorosubstitution; high mobility
Year: 2017 PMID: 28736833 DOI: 10.1002/adma.201702115
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849