Issue 6, 2022

Twisted tetrathiafulvalene crystals

Abstract

Optically-active optoelectronic materials are of great interest for many applications, including chiral sensing and circularly polarized light emission. Traditionally, such applications have been enabled by synthetic strategies to design chiral organic semiconductors and conductors. Here, centrosymmetric tetrathiafulvalene (TTF) crystals are rendered chiral on the mesoscale by crystal twisting. During crystallization from the melt, helicoidal TTF fibers were observed to grow radially outwards from a nucleation centre as spherulites, twisting in concert about the growth direction. Because molecular crystals exhibit orientation-dependent refractive indices, periodic concentric bands associated with continually rotating crystal orientations were observed within the spherulites when imaged between crossed polarizers. Under certain conditions, concomitant crystal twisting and bending was observed, resulting in anomolous crystal optical behavior. X-ray diffraction measurements collected on different spherulite bands indicated no difference in the molecular packing between straight and twisted TTF crystals, as expected for microscopic twisting pitches between 20–200 μm. Mueller matrix imaging, however, revealed preferential absorption and refraction of left- or right-circularly polarized light in twisted crystals depending on the twist sense, either clockwise or counterclockwise, about the growth direction. Furthermore, hole mobilities of 2.0 ± 0.9 × 10−6 cm2 V−1 s−1 and 1.9 ± 0.8 × 10−5 cm2 V−1 s−1 were measured for straight and twisted TTF crystals deposited on organic field-effect transistor platforms, respectively, demonstrating that crystal twisting does not negatively impact charge transport in these systems.

Graphical abstract: Twisted tetrathiafulvalene crystals

Article information

Article type
Paper
Submitted
21 Jan 2022
Accepted
16 Feb 2022
First published
16 Feb 2022

Mol. Syst. Des. Eng., 2022,7, 569-576

Author version available

Twisted tetrathiafulvalene crystals

Y. Yang, K. Zong, St. J. Whittaker, Z. An, M. Tan, H. Zhou, A. G. Shtukenberg, B. Kahr and S. S. Lee, Mol. Syst. Des. Eng., 2022, 7, 569 DOI: 10.1039/D2ME00010E

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