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Ion transport and limited currents in supporting electrolytes and ionic liquids
Supporting electrolytes contain inert dissolved salts to increase the conductivity, to change microenvironments near the electrodes and to assist in electrochemical reactions. This combined experimental and computational study examines the impact of supporting salts on the ion transport and related ...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9008042/ https://www.ncbi.nlm.nih.gov/pubmed/35418198 http://dx.doi.org/10.1038/s41598-022-10183-2 |
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author | Schalenbach, Maximilian Durmus, Yasin Emre Tempel, Hermann Kungl, Hans Eichel, Rüdiger-A. |
author_facet | Schalenbach, Maximilian Durmus, Yasin Emre Tempel, Hermann Kungl, Hans Eichel, Rüdiger-A. |
author_sort | Schalenbach, Maximilian |
collection | PubMed |
description | Supporting electrolytes contain inert dissolved salts to increase the conductivity, to change microenvironments near the electrodes and to assist in electrochemical reactions. This combined experimental and computational study examines the impact of supporting salts on the ion transport and related limited currents in electrochemical cells. A physical model that describes the multi-ion transport in liquid electrolytes and the resulting concentration gradients is presented. This model and its parameterization are evaluated by the measured limited current of the copper deposition in a CuSO(4) electrolyte under a gradually increasing amount of Na(2)SO(4) that acts as a supporting salt. A computational sensibility analysis of the transport model reveals that the shared conductance between the ions lowers the limited currents with larger supporting salt concentrations. When the supporting salt supplies most of the conductance, the electric-field-driven transport of the electrochemically active ions becomes negligible so that the limited current drops to the diffusion-limited current that is described by Fick’s first law. The transition from diluted supporting electrolyte to the case of ionic liquids is elucidated with the transport model, highlighting the different physical transport mechanisms in a non-conducting (polar) and a conducting (ionic) solvent. |
format | Online Article Text |
id | pubmed-9008042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90080422022-04-15 Ion transport and limited currents in supporting electrolytes and ionic liquids Schalenbach, Maximilian Durmus, Yasin Emre Tempel, Hermann Kungl, Hans Eichel, Rüdiger-A. Sci Rep Article Supporting electrolytes contain inert dissolved salts to increase the conductivity, to change microenvironments near the electrodes and to assist in electrochemical reactions. This combined experimental and computational study examines the impact of supporting salts on the ion transport and related limited currents in electrochemical cells. A physical model that describes the multi-ion transport in liquid electrolytes and the resulting concentration gradients is presented. This model and its parameterization are evaluated by the measured limited current of the copper deposition in a CuSO(4) electrolyte under a gradually increasing amount of Na(2)SO(4) that acts as a supporting salt. A computational sensibility analysis of the transport model reveals that the shared conductance between the ions lowers the limited currents with larger supporting salt concentrations. When the supporting salt supplies most of the conductance, the electric-field-driven transport of the electrochemically active ions becomes negligible so that the limited current drops to the diffusion-limited current that is described by Fick’s first law. The transition from diluted supporting electrolyte to the case of ionic liquids is elucidated with the transport model, highlighting the different physical transport mechanisms in a non-conducting (polar) and a conducting (ionic) solvent. Nature Publishing Group UK 2022-04-13 /pmc/articles/PMC9008042/ /pubmed/35418198 http://dx.doi.org/10.1038/s41598-022-10183-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Schalenbach, Maximilian Durmus, Yasin Emre Tempel, Hermann Kungl, Hans Eichel, Rüdiger-A. Ion transport and limited currents in supporting electrolytes and ionic liquids |
title | Ion transport and limited currents in supporting electrolytes and ionic liquids |
title_full | Ion transport and limited currents in supporting electrolytes and ionic liquids |
title_fullStr | Ion transport and limited currents in supporting electrolytes and ionic liquids |
title_full_unstemmed | Ion transport and limited currents in supporting electrolytes and ionic liquids |
title_short | Ion transport and limited currents in supporting electrolytes and ionic liquids |
title_sort | ion transport and limited currents in supporting electrolytes and ionic liquids |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9008042/ https://www.ncbi.nlm.nih.gov/pubmed/35418198 http://dx.doi.org/10.1038/s41598-022-10183-2 |
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