Department of Molecular Design and Engineering, Graduate School of Engineering, Nagoya University, Chikusa, Nagoya, Aichi 464-8603, Japan.
J Phys Chem B. 2012 Jun 21;116(24):7322-7. doi: 10.1021/jp3032308. Epub 2012 Jun 7.
The shear relaxation spectra of the solutions of lithium salts in ionic liquids composed of N-methyl-N-propylpyrrolidinium cation paired with bis(trifluoromethanesulfonyl)amide (TFSA(-)) or bis(fluorosulfonyl)amide (FSA(-)) anions are determined from 5 to 205 MHz at various concentrations of lithium salts. The addition of lithium salt retards the shear relaxation, together with the increase in the shear viscosity. The normalized spectra reduce to a single curve when plotted against the product of the frequency and zero-frequency shear viscosity, which indicates that the increase in the shear viscosity by lithium salts is ascribed to the increase in the relaxation time. The difference in the shear viscosity of TFSA- and FSA-based ionic liquids is also elucidated in terms of the shear relaxation time. The relationship with previous studies on ionic mobility and liquid structure is also discussed.
在各种锂盐浓度下,通过 5 至 205 MHz 的测量,确定了由 N-甲基-N-丙基吡咯烷阳离子与双(三氟甲烷磺酰基)酰胺(TFSA(-))或双(氟磺酰基)酰胺(FSA(-))阴离子组成的离子液体中锂盐溶液的剪切松弛谱。锂盐的加入会减缓剪切松弛,同时增加剪切粘度。当将归一化光谱绘制为频率与零频剪切粘度的乘积时,它们会归一到单个曲线,这表明锂盐引起的剪切粘度增加归因于松弛时间的增加。还根据剪切松弛时间阐明了基于 TFSA-和 FSA-的离子液体的剪切粘度差异。还讨论了与离子迁移率和液体结构的先前研究的关系。