Funahashi Masahiro, Koshiba Yasuko, Horike Shohei, Uemura Shinobu
Department of Chemical Science and Engineering, Graduate School of Engineering, Kobe University, Kobe, Japan.
Research Center for Membrane and Film Technology, Kobe University, Kobe, Japan.
Sci Technol Adv Mater. 2025 Jul 1;26(1):2525058. doi: 10.1080/14686996.2025.2525058. eCollection 2025.
Room-temperature bulk photovoltaic effect of a ferroelectric liquid crystal based on diphenylterthiophene bearing dilactate side chains is provided in this study. In the polarized smectic phase of this compound, the improved bulk photovoltaic effect was observed without electron acceptors, indicating the open-circuit voltage of 1.1 V. A time-of-flight measurement revealed that the hole and electron mobilities were retained to be over 1 × 10 cmVs at room temperature. Dielectric relaxation spectra exhibited that the relaxation of dipolar fluctuation shifted from 10 Hz to 10 Hz in the polarized smectic phase, indicating suppression of thermal motion of the polar side chains. By doping a fullerene derivative as an electron acceptor, the performance of the bulk photovoltaic effect was also enhanced at room temperature, indicating the power conversion efficiency of 0.24 %. The double chiral structure of the dilactate side chain should restrict the conformation of the carbonyl groups in the side chains to enhance packing of the π-conjugated units and to stabilize the polarized structure of the smectic phase.
本研究报道了一种基于带有双乳酸侧链的二苯基三联噻吩的铁电液晶的室温体光伏效应。在该化合物的极化近晶相中,无需电子受体即可观察到增强的体光伏效应,开路电压为1.1 V。飞行时间测量表明,在室温下,空穴和电子迁移率保持在1×10 cmVs以上。介电弛豫谱显示,在极化近晶相中,偶极涨落的弛豫从10 Hz移至10 Hz,表明极性侧链的热运动受到抑制。通过掺杂富勒烯衍生物作为电子受体,室温下体光伏效应的性能也得到了增强,功率转换效率为0.24%。双乳酸侧链的双螺旋结构应能限制侧链中羰基的构象,从而增强π共轭单元的堆积,并稳定近晶相的极化结构。