Capacitive energy storage in single-file pores: Exactly-solvable models and simulations
| Autor: | Svyatoslav Kondrat, Taras Verkholyak, A. R. Kuzmak |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2021 |
| Předmět: |
Chemical Physics (physics.chem-ph)
Materials science Differential capacitance media_common.quotation_subject Monte Carlo method Lattice (group) FOS: Physical sciences General Physics and Astronomy Inverse Condensed Matter - Soft Condensed Matter Capacitance Asymmetry Ion Chemical physics Physics - Chemical Physics Soft Condensed Matter (cond-mat.soft) Physical and Theoretical Chemistry Lattice model (physics) media_common |
| Popis: | Understanding charge storage in low-dimensional electrodes is crucial for developing novel ecologically friendly devices for capacitive energy storage and conversion, water desalination, etc. Exactly-solvable models allow in-depth analyses and essential physical insights into the charging mechanisms. So far, however, such analytical approaches have been mainly limited to lattice models. Herein, we develop a versatile, exactly-solvable, one-dimensional off-lattice model for charging single-file pores. Unlike the lattice model, this model shows an excellent quantitative agreement with three-dimensional Monte Carlo simulations. With analytical calculations and simulations, we show that the differential capacitance can be bell-shaped (one peak), camel-shaped (two peaks), or have four peaks. Transformations between these capacitance shapes can be induced by changing pore ionophilicity, cation-anion size asymmetry, or by adding solvent. We find that the camel-shaped capacitance, characteristic of dilute electrolytes, appears for strongly ionophilic pores with high ion densities, which we relate to charging mechanisms specific to narrow pores. We also derive a large-voltage asymptotic expression for the capacitance, showing that the capacitance decays to zero as the inverse square of the voltage, $C \sim u^{-2}$. This dependence follows from hard-core interactions and is not captured by the lattice model. The following article has been accepted by the Journal of Chemical Physics. After it is published, it will be found at https://doi.org/10.1063/5.0066786 . (29 pages, 6 figures) |
| Databáze: | OpenAIRE |
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