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室温离子液体中的取向动力学和平动动力学

Orientational and translational dynamics in room temperature ionic liquids.

作者信息

Rivera A, Brodin A, Pugachev A, Rössler E A

机构信息

Experimentalphysik II, Universität Bayreuth, 95440 Bayreuth, Germany.

出版信息

J Chem Phys. 2007 Mar 21;126(11):114503. doi: 10.1063/1.2712184.

Abstract

The authors investigate the dynamics of a series of room temperature ionic liquids, based on the same 1-butyl-3-methylimidazolium cation with different anions, by means of broadband (10(-6)-10(9) Hz) dielectric spectroscopy and depolarized light scattering in the temperature range from 400 K down to 35 K. Typical ionic conductivity is observed above the glass transition temperature Tg. Below Tg the authors detect relaxation processes that exhibit characteristics of secondary relaxations, as typically observed in molecular glasses. At high temperatures, the characteristic times of cation reorientation, deduced from the light scattering data, are approximately equal to the electric modulus relaxation times related to ionic conductivity. In the supercooled regime and close to Tg, the authors observe decoupling of conductivity from structural relaxation. Overall, room temperature ionic liquids exhibit typical glass transition dynamics, apparently unaltered by Coulomb interactions.

摘要

作者通过宽带(10⁻⁶ - 10⁹ Hz)介电谱和在400 K至35 K温度范围内的去偏振光散射,研究了一系列基于相同的1-丁基-3-甲基咪唑阳离子与不同阴离子的室温离子液体的动力学。在玻璃化转变温度Tg以上观察到典型的离子电导率。在Tg以下,作者检测到表现出次级弛豫特征的弛豫过程,这在分子玻璃中通常可以观察到。在高温下,由光散射数据推导的阳离子重排特征时间大约等于与离子电导率相关的电模量弛豫时间。在过冷状态且接近Tg时,作者观察到电导率与结构弛豫的解耦。总体而言,室温离子液体表现出典型的玻璃化转变动力学,显然未受库仑相互作用的影响。

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