Friebel Patrick, Galimberti Daria Ruth, Savoini Matteo, Cattaneo Laura
Max Planck Institute for Nuclear Physics, Saupfercheckweg 1, Heidelberg 69117, Germany.
Institute for Molecules and Materials, Radboud University, Heyendaalsweg 135, Nijmegen 6526 AJ, The Netherlands.
J Phys Chem B. 2024 Jan 18;128(2):596-602. doi: 10.1021/acs.jpcb.3c07947. Epub 2024 Jan 8.
Liquid crystals have found a wide area of application over the last few decades, proving to be excellent materials for tunable optics from visible to near-infrared frequencies. Currently, much effort is devoted to demonstrating their applicability at THz frequencies (1-10 THz), where tremendous advances of broadband and intense sources have been achieved. Yet, a detailed understanding of THz-triggered dynamics in liquid crystals is incomplete. Here, we perform broadband THz time domain spectroscopy on 4-cyano-4'-alkyl-biphenyl (CB) and 5-phenylcyclohexanes (PCH5) across mesophases. Density functional theory calculations on isolated molecules capture the majority of the response. In particular, the pronounced modes around 4.5 and 5.5 THz mainly originate from bending modes of the cyano group. In contrast, the broad response below 3 THz, linked to modes of the alkyl chain, disagrees with the single molecule calculation. Here, we identify a clear intermolecular character of the response, supported by dimer and trimer calculations.
在过去几十年里,液晶已得到广泛应用,事实证明它是从可见光到近红外频率的可调谐光学领域的优秀材料。目前,人们致力于证明其在太赫兹频率(1 - 10太赫兹)下的适用性,在该频率范围内,宽带和强光源已取得了巨大进展。然而,对液晶中太赫兹触发动力学的详细理解仍不完整。在此,我们对4 - 氰基 - 4'- 烷基 - 联苯(CB)和5 - 苯基环己烷(PCH5)跨中间相进行宽带太赫兹时域光谱分析。对孤立分子的密度泛函理论计算捕捉到了大部分响应。特别是,4.5和5.5太赫兹附近的明显模式主要源于氰基的弯曲模式。相比之下,低于3太赫兹的宽响应与烷基链的模式有关,这与单分子计算结果不一致。在此,我们通过二聚体和三聚体计算确定了响应具有明显的分子间特征。