Department of Chemistry, The Pennsylvania State University, University Park, Pennsylvania 16802, USA.
J Phys Chem B. 2010 Jul 1;114(25):8410-24. doi: 10.1021/jp1004709.
An idealized four-site ionic liquid model having characteristics approximating those of 1-butyl-3-methylimidazolium hexafluorophosphate ([Im(41)][PF(6)]) is introduced as a low-cost alternative to existing all-atom models for purposes of simulating solute-based dynamics over nanosecond and longer time scales. The structural and energetic properties of the model are in reasonable agreement with those of [Im(41)][PF(6)] and similar ionic liquids, but the dynamics are unrealistically slow. A temperature shift of approximately 100 K is required to produce agreement between the viscosity and diffusion coefficients of the model and experimental values. Several aspects of the ion dynamics such as subdiffusive translational motions, non-Gaussian van Hove distributions, and jumplike displacements in both positions and orientations, are similar to behavior observed in supercooled liquids. Translational diffusion coefficients and rotational correlation times show roughly the proportionalities to viscosity expected from hydrodynamic models, and slip hydrodynamic calculations provide reasonable accuracy in some cases. But anomalously high rotational diffusion coefficients which decouple from viscosity at low temperature are also observed. These anomalies are explained in terms of the prevalence of 180 degrees rotational jumps coupled to the presence of marked heterogeneity in rotational motions, especially about one molecular axis. Comparisons between the dynamics observed in the ionic liquid (IL) model and a neutral mixture (NM) counterpart help to explain the origins of the distinctive dynamics in ionic liquids compared to conventional solvents. The requirement for balancing electrostatic interactions in the IL leads to uniform and interleaved distributions of cations and anions resembling a distorted ionic lattice, similar to the structure of molten NaCl. The resistance to reorganizing this structure is what leads to the slow dynamics of ionic liquids. The coupling among large collections of ions is presumably responsible for the similarity of ionic liquids to supercooled conventional liquids.
引入了一个理想化的四站点离子液体模型,该模型具有类似于 1-丁基-3-甲基咪唑六氟磷酸盐([Im(41)][PF(6)])的特性,可作为现有全原子模型的低成本替代品,用于模拟纳秒及更长时间尺度上基于溶质的动力学。该模型的结构和能量特性与[Im(41)][PF(6)]和类似的离子液体相符,但动力学却异常缓慢。需要将温度升高约 100 K,才能使模型的粘度和扩散系数与实验值相符。离子动力学的几个方面,如亚扩散平移运动、非高斯范霍夫分布以及位置和取向的跳跃式位移,与过冷液体中的行为相似。平移扩散系数和旋转相关时间大致表现出与流体力学模型预期的粘度成正比的关系,而滑移流体力学计算在某些情况下提供了合理的准确性。但也观察到了异常高的旋转扩散系数,这些系数在低温下与粘度解耦。这些异常现象可以用 180 度旋转跳跃的普遍性以及旋转运动中明显的异质性来解释,尤其是关于一个分子轴。离子液体(IL)模型和中性混合物(NM)模型之间的动力学比较有助于解释与传统溶剂相比离子液体独特动力学的起源。在 IL 中平衡静电相互作用的要求导致阳离子和阴离子的均匀和交错分布,类似于扭曲的离子晶格,类似于熔融 NaCl 的结构。抵抗重新组织这种结构的能力导致了离子液体的缓慢动力学。大量离子之间的耦合可能是离子液体与过冷传统液体相似的原因。