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太赫兹克尔效应揭示的甲醇介电响应的本质

The Nature of the Dielectric Response of Methanol Revealed by the Terahertz Kerr Effect.

作者信息

Kampfrath Tobias, Campen R Kramer, Wolf Martin, Sajadi Mohsen

机构信息

Fritz-Haber-Institut der Max-Planck-Gesellschaft , Berlin , Germany.

Department of Physics , Freie Universität Berlin , Berlin , Germany.

出版信息

J Phys Chem Lett. 2018 Mar 15;9(6):1279-1283. doi: 10.1021/acs.jpclett.7b03281. Epub 2018 Feb 28.

Abstract

The dielectric response of liquids in the terahertz (THz) and sub-THz frequency range arises from low-energy collective molecular motions, which are often strongly influenced by intermolecular interactions. To shed light on the microscopic origin of the THz dielectric response of the simplest alcohol, methanol, we resonantly excite this liquid with an intense THz electric-field pulse and monitor the relaxation of the induced optical birefringence. We find a unipolar THz-Kerr-effect signal which, in contrast to aprotic polar liquids, shows a weak coupling between the THz electric field and the permanent molecular dipole moment of the liquid. We assign this weak coupling to the restricted translational rather than rotational nature of the excited mode. Our approach opens a new avenue to the assignment of the dielectric spectrum of liquids to a microscopic origin.

摘要

液体在太赫兹(THz)和亚太赫兹频率范围内的介电响应源于低能量的集体分子运动,而这些运动通常受到分子间相互作用的强烈影响。为了阐明最简单的醇类——甲醇的太赫兹介电响应的微观起源,我们用强太赫兹电场脉冲对这种液体进行共振激发,并监测诱导光学双折射的弛豫过程。我们发现了一个单极太赫兹克尔效应信号,与非质子极性液体相比,该信号表明太赫兹电场与液体的永久分子偶极矩之间存在弱耦合。我们将这种弱耦合归因于激发模式的受限平移性质而非旋转性质。我们的方法为将液体介电谱归因于微观起源开辟了一条新途径。

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