Macroscopic conductivity of aqueous electrolyte solutions scales with ultrafast microscopic ion motions

被引:44
作者
Balos, Vasileios [1 ,4 ]
Imoto, Sho [1 ]
Netz, Roland R. [2 ]
Bonn, Mischa [1 ]
Bonthuis, Douwe Jan [2 ,3 ]
Nagata, Yuki [1 ]
Hunger, Johannes [1 ]
机构
[1] Max Planck Inst Polymer Res, Dept Mol Spect, Ackermannweg 10, D-55128 Mainz, Germany
[2] Free Univ Berlin, Fachbereich Phys, Arnimallee 14, D-14195 Berlin, Germany
[3] Graz Univ Technol, Inst Theoret & Computat Phys, Petersgasse 16-2, A-8010 Graz, Austria
[4] Max Planck Gesell, Fritz Haber Inst, Dept Phys Chem, Faradayweg 4-6, D-14195 Berlin, Germany
基金
欧洲研究理事会;
关键词
DIELECTRIC-RELAXATION; TEMPERATURE-DEPENDENCE; WATER DYNAMICS; SPECTROSCOPY; SOLVATION; EXCHANGE; SHELL;
D O I
10.1038/s41467-020-15450-2
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Despite the widespread use of aqueous electrolytes as conductors, the molecular mechanism of ionic conductivity at moderate to high electrolyte concentrations remains largely unresolved. Using a combination of dielectric spectroscopy and molecular dynamics simulations, we show that the absorption of electrolytes at similar to 0.3 THz sensitively reports on the local environment of ions. The magnitude of these high-frequency ionic motions scales linearly with conductivity for a wide range of ions and concentrations. This scaling is rationalized within a harmonic oscillator model based on the potential of mean force extracted from simulations. Our results thus suggest that long-ranged ionic transport is intimately related to the local energy landscape and to the friction for short-ranged ion dynamics: a high macroscopic electrolyte conductivity is thereby shown to be related to large-amplitude motions at a molecular scale.
引用
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页数:8
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