Kinetic dielectric decrement revisited: phenomenology of finite ion concentrations

Literature Information

Publication Date 2014-11-05
DOI 10.1039/C4CP04182H
Impact Factor 3.676
Authors

Marcello Sega, Axel Arnold


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Abstract

With the help of a recently developed non-equilibrium approach, we investigate the ionic strength dependence of the Hubbard–Onsager dielectric decrement. We compute the depolarization of water molecules caused by the motion of ions in sodium chloride solutions from the dilute regime (0.035 M) up close to the saturation concentration (4.24 M), and find that the kinetic decrement displays a strong non-monotonic behavior, in contrast to the prediction of available models. We introduce a phenomenological modification of the Hubbard–Onsager continuum theory, which takes into account the screening due to the ionic cloud at the mean-field level and, which is able to describe the kinetic decrement at high concentrations including the presence of a pronounced minimum.

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DOI: 10.1039/C6CP90036D

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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
Self-citation Rate: 10.3%
Articles per Year: 3036

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

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