González Miguel Angel, Akiba Hiroshi, Borodin Oleg, Cuello Gabriel Julio, Hennet Louis, Kohara Shinji, Maginn Edward J, Mangin-Thro Lucile, Yamamuro Osamu, Zhang Yong, Price David L, Saboungi Marie-Louise
Institut Laue-Langevin, 71 avenue des Martyrs, 38042 Grenoble Cedex 9, France.
Institute for Solid State Physics, University of Tokyo, Kashiwa, Chiba 277-8581, Japan.
Phys Chem Chem Phys. 2022 May 11;24(18):10727-10736. doi: 10.1039/d2cp00537a.
We report a systematic diffraction study of two "water-in-salt" electrolytes and a "water-in-bisalt" electrolyte combining high-energy X-ray diffraction (HEXRD) with polarized and unpolarized neutron diffraction (ND) on both HO and DO solutions. The measurements provide three independent combinations of correlations between the different pairs of atom types that reveal the short- and intermediate-range order in considerable detail. The ND interference functions show pronounced peaks around a scattering vector ∼ 0.5 Å that change dramatically with composition, indicating significant rearrangements of the water network on a length scale around 12 Å. The experimental results are compared with two sets of Molecular Dynamics (MD) simulations, one including polarization effects and the other based on a non-polarizable force field. The two simulations reproduce the general shapes of the experimental structure factors and their changes with concentration, but differ in many detailed respects, suggesting ways in which their force fields might be modified to better represent the actual systems.
我们报告了对两种“盐包水”电解质和一种“双盐包水”电解质的系统衍射研究,该研究在HO和DO溶液上结合了高能X射线衍射(HEXRD)与极化和非极化中子衍射(ND)。这些测量提供了不同原子类型对之间相关性的三种独立组合,相当详细地揭示了短程和中程有序。ND干涉函数在散射矢量约为0.5 Å处显示出明显的峰值,该峰值随组成发生显著变化,表明水网络在约12 Å的长度尺度上发生了重大重排。将实验结果与两组分子动力学(MD)模拟进行了比较,一组包括极化效应,另一组基于非极化力场。这两种模拟再现了实验结构因子的一般形状及其随浓度的变化,但在许多细节方面存在差异,这表明了可能修改其力场以更好地表示实际系统的方法。