合作性
离子
分子
化学
溶剂化壳
化学物理
反离子
高氯酸盐
无机化学
氯化锂
氯化物
碘化物
溶剂化
有机化学
生物化学
作者
Klaas‐Jan Tielrooij,Nuria Garcı́a-Aráez,Mischa Bonn,Huib J. Bakker
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2010-05-20
卷期号:328 (5981): 1006-1009
被引量:625
标识
DOI:10.1126/science.1183512
摘要
Despite prolonged scientific efforts to unravel the effects of ions on the structure and dynamics of water, many open questions remain, in particular concerning the spatial extent of this effect (i.e., the number of water molecules affected) and the origin of ion-specific effects. A combined terahertz and femtosecond infrared spectroscopic study of water dynamics around different ions (specifically magnesium, lithium, sodium, and cesium cations, as well as sulfate, chloride, iodide, and perchlorate anions) reveals that the effect of ions and counterions on water can be strongly interdependent and nonadditive, and in certain cases extends well beyond the first solvation shell of water molecules directly surrounding the ion.
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