Issue 9, 2015

Ferroelectric liquid-crystalline semiconductors based on a phenylterthiophene skeleton: effect of the introduction of oligosiloxane moieties and photovoltaic effect

Abstract

Ferroelectric liquid-crystalline phenylterthiophene derivatives bearing a decenyl group, disiloxane chain, and cyclotetrasiloxane ring were synthesized. These compounds exhibited a chiral smectic C (SmC*) phase. The spontaneous polarizations of the compounds exceeded 50 nC cm−2. The hole mobilities determined by the time-of-flight method were in the order of 1 × 10−4 cm2 V−1 s−1. The compound with a decenyl group exhibited an anomalous photovoltaic effect in the SmC* phase although the conversion efficiency was lower than 0.01%. Notably, even the compound bearing a bulky cyclotetrasiloxane ring exhibited an enantiotropic SmC* phase.

Graphical abstract: Ferroelectric liquid-crystalline semiconductors based on a phenylterthiophene skeleton: effect of the introduction of oligosiloxane moieties and photovoltaic effect

Supplementary files

Article information

Article type
Paper
Submitted
31 Jul 2014
Accepted
14 Dec 2014
First published
17 Dec 2014

J. Mater. Chem. C, 2015,3, 1982-1993

Author version available

Ferroelectric liquid-crystalline semiconductors based on a phenylterthiophene skeleton: effect of the introduction of oligosiloxane moieties and photovoltaic effect

Y. Funatsu, A. Sonoda and M. Funahashi, J. Mater. Chem. C, 2015, 3, 1982 DOI: 10.1039/C4TC01690D

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