离子液体
共晶体系
电化学
化学
溶剂
反应性(心理学)
吉布斯自由能
活度系数
化学稳定性
水活度
化学工程
电导率
热力学
无机化学
深共晶溶剂
水蒸气
离子键合
水的性质
材料科学
溶剂效应
含水量
溶剂化
分子动力学
物理化学
水溶液
C4毫米
液态水
蒸汽压
电化学窗口
分子
有机化学
摩尔电导率
电解质
作者
Desiree Mae Prado,Aaron Niño Gonzaga,Clemens Burda
出处
期刊:ChemPhysChem
[Wiley]
日期:2025-12-16
卷期号:27 (4): e202500510-e202500510
被引量:1
标识
DOI:10.1002/cphc.202500510
摘要
Water is widely recognized as critical to the tunability and electrochemical stability of nonaqueous solvents such as deep eutectic solvents (DESs) and ionic liquids (ILs). Traditionally, the water content of these solvents has been controlled by either drying or adding small amounts of water to control their bulk properties to meet specific application requirements. The total water content by itself, does not provide sufficient information about the chemical reactivity and molecular interactions within DES- and IL-water mixtures. In this concept article, water activity is highlighted as a thermodynamically more rigorous descriptor to quantify the influence of the co-solvent water on DES- and IL-water mixtures. Water activity relates measurable physical properties, such as vapor pressure, density, viscosity, electrochemical stability, and conductivity of DESs and ILs to the underlying molecular interactions between their components. Furthermore, water activity of DESs and ILs correlates with changes in local solvent structures and thermodynamic excess properties, including excess molar volume, enthalpy, and Gibbs energy.
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