Issue 43, 2020

Quinoidal thioalkyl-substituted bithiophene small molecule semiconductors for n-type organic field effect transistors

Abstract

Two tetrathioalkyl-substituted bithiophene-based small molecule quinoids (TSBTQs) having different chain lengths (thio-hexyl and -decyl) are synthesized and applied as an n-type active component in organic field effect transistors (OFETs). The resulting two TSBTQs exhibit good solubility in various organic solvents and LUMO levels below −4.0 eV. The theoretical DFT calculation supported by single crystal structures confirms the π-conjugated backbone planarity due to the S(thiophene)⋯S(alkyl) non-covalent interaction. Optimized TSBQT-10 OFETs exhibit an electron mobility of 0.18 cm2 V−1 s−1, which is higher than that of TSBTQ-6 (0.09 cm2 V−1 s−1). The reliability of the OFETs under representative environmental and operational conditions is also determined. The effects of side chains including their lengths and contribution to the main chain π-system coplanarity presented here demonstrate an efficient method to manipulate the charge carrier mobility of the quinoidal organic semiconductors.

Graphical abstract: Quinoidal thioalkyl-substituted bithiophene small molecule semiconductors for n-type organic field effect transistors

Supplementary files

Article information

Article type
Paper
Submitted
10 Aug. 2020
Accepted
21 Sept. 2020
First published
23 Sept. 2020

J. Mater. Chem. C, 2020,8, 15450-15458

Quinoidal thioalkyl-substituted bithiophene small molecule semiconductors for n-type organic field effect transistors

V. Joseph, C. Yu, C. Lin, W. Lien, H. Tsai, C. Chen, A. A. A. Torimtubun, A. Velusamy, P. Huang, G. Lee, S. Yau, S. Tung, T. Minari, C. Liu and M. Chen, J. Mater. Chem. C, 2020, 8, 15450 DOI: 10.1039/D0TC03808C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements