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Enhancing Hydrophilicity of Thick Electrodes for High Energy Density Aqueous Batteries

Thick electrodes can substantially enhance the overall energy density of batteries. However, insufficient wettability of aqueous electrolytes toward electrodes with conventional hydrophobic binders severely limits utilization of active materials with increasing the thickness of electrodes for aqueou...

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Autores principales: Lee, Jungeun, Lee, Hyeonsoo, Bak, Cheol, Hong, Youngsun, Joung, Daeha, Ko, Jeong Beom, Lee, Yong Min, Kim, Chanhoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10086092/
https://www.ncbi.nlm.nih.gov/pubmed/37038025
http://dx.doi.org/10.1007/s40820-023-01072-y
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author Lee, Jungeun
Lee, Hyeonsoo
Bak, Cheol
Hong, Youngsun
Joung, Daeha
Ko, Jeong Beom
Lee, Yong Min
Kim, Chanhoon
author_facet Lee, Jungeun
Lee, Hyeonsoo
Bak, Cheol
Hong, Youngsun
Joung, Daeha
Ko, Jeong Beom
Lee, Yong Min
Kim, Chanhoon
author_sort Lee, Jungeun
collection PubMed
description Thick electrodes can substantially enhance the overall energy density of batteries. However, insufficient wettability of aqueous electrolytes toward electrodes with conventional hydrophobic binders severely limits utilization of active materials with increasing the thickness of electrodes for aqueous batteries, resulting in battery performance deterioration with a reduced capacity. Here, we demonstrate that controlling the hydrophilicity of the thicker electrodes is critical to enhancing the overall energy density of batteries. Hydrophilic binders are synthesized via a simple sulfonation process of conventional polyvinylidene fluoride binders, considering physicochemical properties such as mechanical properties and adhesion. The introduction of abundant sulfonate groups of binders (i) allows fast and sufficient electrolyte wetting, and (ii) improves ionic conduction in thick electrodes, enabling a significant increase in reversible capacities under various current densities. Further, the sulfonated binder effectively inhibits the dissolution of cathode materials in reactive aqueous electrolytes. Overall, our findings significantly enhance the energy density and contribute to the development of practical zinc-ion batteries. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40820-023-01072-y.
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spelling pubmed-100860922023-04-12 Enhancing Hydrophilicity of Thick Electrodes for High Energy Density Aqueous Batteries Lee, Jungeun Lee, Hyeonsoo Bak, Cheol Hong, Youngsun Joung, Daeha Ko, Jeong Beom Lee, Yong Min Kim, Chanhoon Nanomicro Lett Article Thick electrodes can substantially enhance the overall energy density of batteries. However, insufficient wettability of aqueous electrolytes toward electrodes with conventional hydrophobic binders severely limits utilization of active materials with increasing the thickness of electrodes for aqueous batteries, resulting in battery performance deterioration with a reduced capacity. Here, we demonstrate that controlling the hydrophilicity of the thicker electrodes is critical to enhancing the overall energy density of batteries. Hydrophilic binders are synthesized via a simple sulfonation process of conventional polyvinylidene fluoride binders, considering physicochemical properties such as mechanical properties and adhesion. The introduction of abundant sulfonate groups of binders (i) allows fast and sufficient electrolyte wetting, and (ii) improves ionic conduction in thick electrodes, enabling a significant increase in reversible capacities under various current densities. Further, the sulfonated binder effectively inhibits the dissolution of cathode materials in reactive aqueous electrolytes. Overall, our findings significantly enhance the energy density and contribute to the development of practical zinc-ion batteries. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40820-023-01072-y. Springer Nature Singapore 2023-04-10 /pmc/articles/PMC10086092/ /pubmed/37038025 http://dx.doi.org/10.1007/s40820-023-01072-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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
Lee, Jungeun
Lee, Hyeonsoo
Bak, Cheol
Hong, Youngsun
Joung, Daeha
Ko, Jeong Beom
Lee, Yong Min
Kim, Chanhoon
Enhancing Hydrophilicity of Thick Electrodes for High Energy Density Aqueous Batteries
title Enhancing Hydrophilicity of Thick Electrodes for High Energy Density Aqueous Batteries
title_full Enhancing Hydrophilicity of Thick Electrodes for High Energy Density Aqueous Batteries
title_fullStr Enhancing Hydrophilicity of Thick Electrodes for High Energy Density Aqueous Batteries
title_full_unstemmed Enhancing Hydrophilicity of Thick Electrodes for High Energy Density Aqueous Batteries
title_short Enhancing Hydrophilicity of Thick Electrodes for High Energy Density Aqueous Batteries
title_sort enhancing hydrophilicity of thick electrodes for high energy density aqueous batteries
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10086092/
https://www.ncbi.nlm.nih.gov/pubmed/37038025
http://dx.doi.org/10.1007/s40820-023-01072-y
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