小角X射线散射
溶剂化
材料科学
电解质
纳米结构
化学物理
表征(材料科学)
纳米技术
分子动力学
散射
化学工程
离子液体
离子
物理化学
计算化学
化学
有机化学
光学
物理
电极
工程类
催化作用
作者
Kun Qian,Randall E. Winans,Tao Li
标识
DOI:10.1002/aenm.202002821
摘要
Abstract 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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