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    Experimental Evidence of Long-Lived Electric Fields of Ionic Liquid Bilayers

    90303.pdf (1.195Mb)
    Access Status
    Open access
    Authors
    Belotti, Mattia
    Lyu, Xin
    Xu, L.
    Halat, P.
    Darwish, Nadim
    Silvester-Dean, Debbie
    Goh, Ching
    Izgorodina, E.I.
    Coote, M.L.
    Ciampi, Simone
    Date
    2021
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Belotti, M. and Lyu, X. and Xu, L. and Halat, P. and Darwish, N. and Silvester, D.S. and Goh, C. et al. 2021. Experimental Evidence of Long-Lived Electric Fields of Ionic Liquid Bilayers. Journal of the American Chemical Society. 143 (42): pp. 17431-17440.
    Source Title
    Journal of the American Chemical Society
    DOI
    10.1021/jacs.1c06385
    ISSN
    0002-7863
    Faculty
    Faculty of Science and Engineering
    School
    School of Molecular and Life Sciences (MLS)
    Science and Engineering Technical
    Funding and Sponsorship
    http://purl.org/au-research/grants/arc/DP190100735
    http://purl.org/au-research/grants/arc/FT190100148
    http://purl.org/au-research/grants/arc/FL170100041
    Remarks

    This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of the American Chemical Society, copyright © American Chemical Society, after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/jacs.1c06385.

    URI
    http://hdl.handle.net/20.500.11937/90479
    Collection
    • Curtin Research Publications
    Abstract

    Herein we demonstrate that ionic liquids can form long-lived double layers, generating electric fields detectable by straightforward open circuit potential (OCP) measurements. In imidazolium-based ionic liquids an external negative voltage pulse leads to an exceedingly stable near-surface dipolar layer, whose field manifests as long-lived (∼1-100 h) discrete plateaus in OCP versus time traces. These plateaus occur within an ionic liquid-specific and sharp potential window, defining a simple experimental method to probe the onset of interfacial ordering phenomena, such as overscreening and crowding. Molecular dynamics modeling reveals that the OCP arises from the alignment of the individual ion dipoles to the external electric field pulse, with the magnitude of the resulting OCP correlating with the product of the projected dipole moment of the cation and the ratio between the cation diffusion coefficient and its volume. Our findings also reveal that a stable overscreened structure is more likely to form if the interface is first forced through crowding, possibly accounting for the scattered literature data on relaxation kinetics of near-surface structures in ionic liquids.

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