Abstract
Solution-crystallizable small-molecule organic semiconductors, such as 6,13-bis(triisopropylsilylethynyl)pentacene (TIPS pentacene), 5,11-bis(triethylgermylethynyl)anthradithiophene (diF-TEG-ADT), 2,7-dioctyl[1]benzothieno[3,2-b][1]benzothiophene (C8-BTBT), and N,N′-1H,1H-perfluorobutyl dicyanoperylenecarboxydiimide (PDIF-CN2), demonstrate various practical advantages including high mobility, air stability and solution processibility. In this article, we review various polymer additive based approaches to control the crystal morphology and the resultant charge transport of some bench-mark, high performance, solution crystallizable, small-molecule organic semiconductors. The polymer additives are discussed under the categories of non-conjugated polymers and conjugated polymers. The approaches and structure-performance correlations that we discussed here may be applied far beyond the examples shown in this review and have important implications for high performance organic semiconductors in general.
Original language | English |
---|---|
Pages (from-to) | 5790-5803 |
Number of pages | 14 |
Journal | Soft Matter |
Volume | 15 |
Issue number | 29 |
DOIs | |
State | Published - 2019 |
Funding
This work was supported by the National Science Foundation (NSF) (no. ECCS-1151140) and a postdoctoral research fellowship from the University of Alabama. A part of this research was conducted at the Center for Nanophase Materials Sciences, which is a DOE Office of Science User Facility.