溶剂化
硫酸
化学
电解质
位阻效应
对分布函数
化学物理
溶剂化壳
相(物质)
分子
结晶学
无机化学
物理化学
立体化学
有机化学
物理
电极
量子力学
作者
Tiffany L. Kinnibrugh,T. T. Fister
标识
DOI:10.1021/acs.jpcb.2c00523
摘要
Solvation and mesoscale ordering of sulfuric acid and other strong acid solutions leads to suppressed freezing points and strong rheological changes with varying concentration. While the solid-state structures are well-understood, studies focused on the evolving solvation structure in the solution phase have probed a limited concentration range (∼1-6 M). This study applies a total scattering approach in both the wide-angle X-ray scattering (WAXS) and pair distribution function (PDF) regimes to elucidate the evolving solvation structure over its full range of acid concentration (0-18 M). The emergence of a prepeak in the WAXS regime at intermediate concentrations indicates a transition from noninteracting sulfate molecules in the dilute limit to sterically limited sulfates at concentrations near its deep eutectic point. Fits to the PDF data quantify this trend, showing a transition from octahedrally hydrated sulfates up to 6-7 M concentrations, followed by gradual dehydration, and eventually reaching a solution structure similar to that of water-in-salt electrolyte systems at high acid concentrations.
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