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Association–Dissociation Dynamics of Ionic Electrolytes in Low Dielectric Medium

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dc.contributor.advisor Bagchi, Sayan
dc.contributor.author Ghosh, Deborin
dc.contributor.author Sakpal, Sushil
dc.contributor.author Chatterjee, Srijan
dc.contributor.author Deshmukh, Samadhan
dc.contributor.author Kwon, Hyejin
dc.contributor.author Kim, Yung Sam
dc.contributor.author Bagchi, Sayan
dc.date.accessioned 2023-10-10T06:19:22Z
dc.date.available 2023-10-10T06:19:22Z
dc.date.issued 2021-12-27
dc.identifier.other https://doi.org/10.1021/acs.jpcb.1c08613
dc.identifier.uri https://hdl.handle.net/20.500.12252/6252
dc.description.abstract Ionic electrolytes are known to form various complexes which exist in dynamic equilibrium in a low dielectric medium. However, structural characterization of these complexes has always posed a great challenge to the scientific community. An additional challenge is the estimation of the dynamic association–dissociation time scales (lifetime of the complexes), which are key to the fundamental understanding of ion transport. In this work, we have used a combination of infrared absorption spectroscopy, two-dimensional infrared spectroscopy, molecular dynamics simulations, and density functional theory calculations to characterize the various ion complexes formed by the thiocyanate-based ionic electrolytes as a function of different cations in a low dielectric medium. Our results demonstrate that thiocyanate is an excellent vibrational reporter of the heterogeneous ion complexes undergoing association–dissociation dynamics. We find that the ionic electrolytes exist as contact ion pairs, dimers, and clusters in a low dielectric medium. The relative ratios of the various ion complexes are sensitive to the cations. In addition to the interactions between the thiocyanate anion and the countercation, the solute–solvent interactions drive the dynamic equilibrium. We have estimated the association–dissociation dynamics time scales from two-dimensional infrared spectroscopy. The exchange time scale involving the cluster is faster than that between a dimer and an ion pair. Moreover, we find that the dynamic equilibrium between the cluster and another ion complex is correlated to the solvent fluctuations. en
dc.format.extent 10 en
dc.language.iso en_US en
dc.publisher The Journal of Physical Chemistry B en
dc.subject Ionic liquids en
dc.title Association–Dissociation Dynamics of Ionic Electrolytes in Low Dielectric Medium en
dc.type Article en
local.division.division Physical and Materials Chemistry Division en
dc.description.university -- en


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