The electrostatic screening properties of ionic fluids are of paramount importance in countless physical processes. Yet the screening behavior of ionic conductors out of thermal equilibrium has to date mainly been studied in the context of thermoelectric phenomena by virtue of direct extensions of Debye-Hückel theories. We investigate how the static response of a symmetric ionic fluid is influenced by the presence of a thermal gradient by introducing a theory of electrostatic screening under a stationary temperature profile. By borrowing mathematical methods commonly used in the semiclassical approximation of quantum particles, we find analytical solutions to the asymptotic decay of the charge density which can be used to describe the nonequilibrium response of the system to external charge perturbations and for arbitrary ionic concentrations. Notably, a transition between monotonic and oscillatory screening regimes is observed as an effect of the temperature variation which generalizes known results of thermal equilibrium to out of equilibrium conditions. A final quantitative example on the screening of charged surfaces in aqueous electrolytes shows that the deviation from thermal equilibrium predicted by our solutions is generally larger than thermoelectric effects and should therefore be taken into account for a comprehensive description of the electrical double layer. Our findings pave the way to the rigorous treatment of nonequilibrium steady states in ionic systems with potential applications to the study of energy materials, nanostructured systems, and waste-heat-recovery technologies.
Effect of a temperature gradient on the screening properties of ionic fluids / Grisafi, Andrea; Grasselli, Federico. - In: PHYSICAL REVIEW MATERIALS. - ISSN 2475-9953. - 7:4(2023), pp. 045803-1-045803-10. [10.1103/PhysRevMaterials.7.045803]
Effect of a temperature gradient on the screening properties of ionic fluids
Grasselli Federico
2023
Abstract
The electrostatic screening properties of ionic fluids are of paramount importance in countless physical processes. Yet the screening behavior of ionic conductors out of thermal equilibrium has to date mainly been studied in the context of thermoelectric phenomena by virtue of direct extensions of Debye-Hückel theories. We investigate how the static response of a symmetric ionic fluid is influenced by the presence of a thermal gradient by introducing a theory of electrostatic screening under a stationary temperature profile. By borrowing mathematical methods commonly used in the semiclassical approximation of quantum particles, we find analytical solutions to the asymptotic decay of the charge density which can be used to describe the nonequilibrium response of the system to external charge perturbations and for arbitrary ionic concentrations. Notably, a transition between monotonic and oscillatory screening regimes is observed as an effect of the temperature variation which generalizes known results of thermal equilibrium to out of equilibrium conditions. A final quantitative example on the screening of charged surfaces in aqueous electrolytes shows that the deviation from thermal equilibrium predicted by our solutions is generally larger than thermoelectric effects and should therefore be taken into account for a comprehensive description of the electrical double layer. Our findings pave the way to the rigorous treatment of nonequilibrium steady states in ionic systems with potential applications to the study of energy materials, nanostructured systems, and waste-heat-recovery technologies.File | Dimensione | Formato | |
---|---|---|---|
PhysRevMaterials.7.045803.pdf
Accesso riservato
Tipologia:
Versione pubblicata dall'editore
Dimensione
539.44 kB
Formato
Adobe PDF
|
539.44 kB | Adobe PDF | Visualizza/Apri Richiedi una copia |
Pubblicazioni consigliate
I metadati presenti in IRIS UNIMORE sono rilasciati con licenza Creative Commons CC0 1.0 Universal, mentre i file delle pubblicazioni sono rilasciati con licenza Attribuzione 4.0 Internazionale (CC BY 4.0), salvo diversa indicazione.
In caso di violazione di copyright, contattare Supporto Iris