Insights into the Nanostructure, Solvation, and Dynamics of Liquid Electrolytes through Small-Angle X-Ray Scattering

被引:62
作者
Qian, Kun [1 ]
Winans, Randall E. [2 ,3 ]
Li, Tao [1 ,2 ,3 ]
机构
[1] Northern Illinois Univ, Dept Chem & Biochem, De Kalb, IL 60115 USA
[2] Argonne Natl Lab, Xray Sci Div, Lemont, IL 60439 USA
[3] Argonne Natl Lab, Joint Ctr Energy Storage Res, Lemont, IL 60439 USA
关键词
electrolytes; intermolecular relation; nanostructure; small-angle X-ray scattering; SAXS; AMORPHOUS CONCENTRATED LIQUID; LI-ION; DIFFRACTION; METAL; SOLUBILITY; BATTERIES; MIXTURES; LITFSI; MODELS;
D O I
10.1002/aenm.202002821
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The fundamental understanding of nanostructures of liquid electrolytes is expected to enable transformative gains in electrochemical energy storage capacities. However, the solvation structures and molecular dynamics in electrolytes are hard to probe, which limits further performance improvements in macroscopic properties such as ionic conductivity, viscosity, and stability. Small-angle X-ray scattering (SAXS), a non-destructive method for nanostructures characterization in liquids, offers a unique perspective on molecular clusters, anion-cation pairs, solvation sheath, percolating network, aggregates, and domain sizes of electrolytes. Notably, the SAXS method has excellent time-resolution, enabling the study of molecular dynamics by operando characterization. This review focuses on the microscopic understanding of liquid electrolytes by SAXS and operando SAXS. The unique capabilities of X-ray scattering for intra- and inter-molecular relationship and nanostructure characterization of electrolytes are highlighted.
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页数:22
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