| Literature DB >> 33437584 |
Arulmozhi Velusamy1, Chih-Hsin Yu2, Shakil N Afraj1, Chia-Chi Lin2, Wei-Yu Lo1, Chia-Jung Yeh1, Ya-Wen Wu1, Hsin-Chun Hsieh1, Jianhua Chen3, Gene-Hsiang Lee4, Shih-Huang Tung5, Cheng-Liang Liu6, Ming-Chou Chen1, Antonio Facchetti3.
Abstract
A novel quinoidal thienoisoindigo (TII)-containing small molecule family with dicyanomethylene end-capping units and various alkyl chains is synthesized as n-type organic small molecules for solution-processable organic field effect transistors (OFETs). The molecular structure of the 2-hexyldecyl substituted derivative, TIIQ-b16, is determined via single-crystal X-ray diffraction and shows that the TIIQ core is planar and exhibits molecular layers stacked in a "face-to-face" arrangement with short core intermolecular distances of 3.28 Å. The very planar core structure, shortest intermolecular N···H distance (2.52 Å), existence of an intramolecular non-bonded contact between sulfur and oxygen atom (S···O) of 2.80 Å, and a very low-lying LUMO energy level of -4.16 eV suggest that TIIQ molecules should be electron transporting semiconductors. The physical, thermal, and electrochemical properties as well as OFET performance and thin film morphologies of these new TIIQs are systematically studied. Thus, air-processed TIIQ-b16 OFETs exhibit an electron mobility up to 2.54 cm2 V-1 s-1 with a current ON/OFF ratio of 105-106, which is the first demonstration of TII-based small molecules exhibiting unipolar electron transport characteristics and enhanced ambient stability. These results indicate that construction of quinoidal molecule from TII moiety is a successful approach to enhance n-type charge transport characteristics.Entities:
Keywords: organic field effect transistors; organic semiconductors; quinoid; solution‐shearing; thienoisoindigo
Year: 2020 PMID: 33437584 PMCID: PMC7788596 DOI: 10.1002/advs.202002930
Source DB: PubMed Journal: Adv Sci (Weinh) ISSN: 2198-3844 Impact factor: 16.806