Issue 18, 2016

On the impact of isomer structure and packing disorder in thienoacene organic semiconductors

Abstract

Many high performing organic semiconductor materials contain heteroaromatic rings in order to control the molecular packing and material electronic properties. Here we use a combination of density functional theory and symmetry-adapted perturbation theory calculations to explore the intermolecular noncovalent interactions, which guide solid-state molecular packing, and electronic couplings in a series of benzodithiophene-based dimer models. A novel concept, termed the disordermer, is introduced to delineate how the reduced molecular symmetry of benzodithiophene, when compared to the more highly symmetric anthracene molecule, can present intermolecular isomerism in the solid state that results in a wide range of available molecular packing arrangements that in turn influence the magnitudes of the electronic couplings. The insight developed through the investigation of these disordermers is demonstrated to hold important implications in the design of new generations of organic semiconductor materials.

Graphical abstract: On the impact of isomer structure and packing disorder in thienoacene organic semiconductors

Supplementary files

Article information

Article type
Paper
Submitted
08 صفر 1437
Accepted
02 جمادى الثانية 1437
First published
02 جمادى الثانية 1437

J. Mater. Chem. C, 2016,4, 4040-4048

On the impact of isomer structure and packing disorder in thienoacene organic semiconductors

K. J. Thorley and C. Risko, J. Mater. Chem. C, 2016, 4, 4040 DOI: 10.1039/C5TC03900B

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