Extremely slow dynamics of ionic liquid self-assembled nanostructures near a solid surface
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Updated: Aug 22, 2025

Liquid-cell Transmission Electron Microscopy for Tracking Self-assembly of Nanoparticles
Published on: October 16, 2017
Hua Li1, Jianan Wang2, Gregory G Warr3
1School of Molecular Sciences, The University of Western Australia, Perth, Western Australia, Australia; Centre for Microscopy, Characterisation and Analysis, The University of Western Australia, Perth, Western Australia, Australia.
Hypothesis:
The dynamics of the self-assembled liquid nanostructure of the ionic liquids (ILs) near a mica surface can be determined from video-rate atomic force microscopy (AFM) data.
Experiments:
Video-rate AFM has been used to record the nanostructure dynamics of two most widely studied ILs, 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (BMIM TFSI) and ethylammonium nitrate (EAN), as well as EAN-water mixtures, above a model anode, mica. Diffusion coefficients were extracted from the AFM videos using dynamic differential microscopy and direct tracking.
Findings:
Video rate AFM is able to record the movement of the IL nanostructure. This is the first time that any liquid has been directly visualized at a scale of 10 nm × 10 nm in real-time. Diffusion coefficients determined from AFM videos reveal IL nanostructures near surfaces diffuse orders of magnitude more slowly than individual ions in the bulk. Thus, rather than free-flowing liquid, the near-surface nanostructure is better conceptualized as self-assembled aggregates of IL ions diffusing slowly over the cation-rich Stern layer, akin to adsorbed surfactant micelles in aqueous systems. This new and surprising insight affects wide-ranging processes involving the interfacial dynamics of concentrated electrolytes.
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