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Electrochemical cell recharging by solvent separation and transfer processes
Electrochemical conversion and storage of unutilized renewable energy will contribute to decarbonization. Here, we create the concept of a liquid electrochemical cell that discharges between the anodic and cathodic sides by reverse reactions of the same redox couple in different solvation states, wh...
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/PMC8904837/ https://www.ncbi.nlm.nih.gov/pubmed/35260617 http://dx.doi.org/10.1038/s41598-022-07573-x |
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author | Matsui, Yohei Kawase, Makoto Suzuki, Takahiro Tsushima, Shohji |
author_facet | Matsui, Yohei Kawase, Makoto Suzuki, Takahiro Tsushima, Shohji |
author_sort | Matsui, Yohei |
collection | PubMed |
description | Electrochemical conversion and storage of unutilized renewable energy will contribute to decarbonization. Here, we create the concept of a liquid electrochemical cell that discharges between the anodic and cathodic sides by reverse reactions of the same redox couple in different solvation states, which are created by differences in the mixture ratios of two solvents called the main solvent (MS) and the transferred solvent (TS). The cell can be charged by a transfer of the TS between the discharged anolyte and catholyte. As an example, we demonstrate a cell utilizing a ferro-/ferricyanide redox couple. Stable discharging and charging via the proposed method is achieved by utilizing water (MS) and acetone (TS). Additionally, dominating factors in the design of a high-performance system are discussed, focusing on the electron acceptability of the MS and the TS. The cell voltages are successfully tuned, and a cell voltage of 0.63 V is achieved by the combination of dimethyl sulfoxide (MS) and water (TS). Moreover, the cell can be customized by various electrochemical reaction systems, which can allow multiple options for the charging processes. This concept provides new approaches for the utilization of diverse energy sources as an input for the charging of electrochemical cells. |
format | Online Article Text |
id | pubmed-8904837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89048372022-03-10 Electrochemical cell recharging by solvent separation and transfer processes Matsui, Yohei Kawase, Makoto Suzuki, Takahiro Tsushima, Shohji Sci Rep Article Electrochemical conversion and storage of unutilized renewable energy will contribute to decarbonization. Here, we create the concept of a liquid electrochemical cell that discharges between the anodic and cathodic sides by reverse reactions of the same redox couple in different solvation states, which are created by differences in the mixture ratios of two solvents called the main solvent (MS) and the transferred solvent (TS). The cell can be charged by a transfer of the TS between the discharged anolyte and catholyte. As an example, we demonstrate a cell utilizing a ferro-/ferricyanide redox couple. Stable discharging and charging via the proposed method is achieved by utilizing water (MS) and acetone (TS). Additionally, dominating factors in the design of a high-performance system are discussed, focusing on the electron acceptability of the MS and the TS. The cell voltages are successfully tuned, and a cell voltage of 0.63 V is achieved by the combination of dimethyl sulfoxide (MS) and water (TS). Moreover, the cell can be customized by various electrochemical reaction systems, which can allow multiple options for the charging processes. This concept provides new approaches for the utilization of diverse energy sources as an input for the charging of electrochemical cells. Nature Publishing Group UK 2022-03-08 /pmc/articles/PMC8904837/ /pubmed/35260617 http://dx.doi.org/10.1038/s41598-022-07573-x 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 Matsui, Yohei Kawase, Makoto Suzuki, Takahiro Tsushima, Shohji Electrochemical cell recharging by solvent separation and transfer processes |
title | Electrochemical cell recharging by solvent separation and transfer processes |
title_full | Electrochemical cell recharging by solvent separation and transfer processes |
title_fullStr | Electrochemical cell recharging by solvent separation and transfer processes |
title_full_unstemmed | Electrochemical cell recharging by solvent separation and transfer processes |
title_short | Electrochemical cell recharging by solvent separation and transfer processes |
title_sort | electrochemical cell recharging by solvent separation and transfer processes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8904837/ https://www.ncbi.nlm.nih.gov/pubmed/35260617 http://dx.doi.org/10.1038/s41598-022-07573-x |
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