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Vibrational dynamics and structural relaxation in aqueous electrolyte solutions in the liquid, undercooled liquid and glassy states

机译:液体,过冷液体和玻璃状液体电解质溶液中的振动动力学和结构松弛

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摘要

In very concentrated aqueous electrolyte solutions, the competition between dipolar and ionic forces and most of the system properties, are finely monitored by the concentration. For LiCl, RH2O (R being the number of water moles per mole of salt) two domains of concentration exist around even hydration numbers R = 6 and R = 4, which can be reversibly undercooled from the liquid to the glassy state. At other concentrations, for [MATH], metastability is achieved only in a restricted temperature range. The collective behaviour as well as individual atomic motions, have been studied by neutron inelastic scattering in the metastable state of LiCl, 6H2O and LiCl, 4H2O down to the glass transition. The study of the structural relaxation by neutron spin echo (NSE) allows us to show that the temperature dependence of the response of the system follows a scaling relation with a cross-over at a phase transition present in the liquid phase.
机译:在非常浓缩的水电解质溶液中,通过浓度细细地监测偶极和离子力与大部分系统性能之间的竞争。对于LiCl,RH2O(R是每摩尔盐的水摩尔数)甚至存在均匀的浓度域甚至是均匀的r = 6和r = 4,其可以从液体到玻璃状状态可逆地过冷却。在其他浓度下,对于[MATH],仅在限制温度范围内实现延展性。通过LICL,6H2O和LICL的亚稳态中的中子空间散射研究了集体行为以及单独的原子动作,将4H2O下降至玻璃化转变。通过中子旋转回波(NSE)的结构弛豫的研究允许我们表明系统响应的温度依赖性跟随液相中存在的相变的横跨的缩放关系。

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