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Raising the redox potential in carboxyphenolate-based positive organic materials via cation substitution
Meeting the ever-growing demand for electrical storage devices requires both superior and “greener” battery technologies. Nearly 40 years after the discovery of conductive polymers, long cycling stability in lithium organic batteries has now been achieved. However, the synthesis of high-voltage lith...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199296/ https://www.ncbi.nlm.nih.gov/pubmed/30353001 http://dx.doi.org/10.1038/s41467-018-06708-x |
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author | Jouhara, Alia Dupré, Nicolas Gaillot, Anne-Claire Guyomard, Dominique Dolhem, Franck Poizot, Philippe |
author_facet | Jouhara, Alia Dupré, Nicolas Gaillot, Anne-Claire Guyomard, Dominique Dolhem, Franck Poizot, Philippe |
author_sort | Jouhara, Alia |
collection | PubMed |
description | Meeting the ever-growing demand for electrical storage devices requires both superior and “greener” battery technologies. Nearly 40 years after the discovery of conductive polymers, long cycling stability in lithium organic batteries has now been achieved. However, the synthesis of high-voltage lithiated organic cathode materials is rather challenging, so very few examples of all-organic lithium-ion cells currently exist. Herein, we present an inventive chemical approach leading to a significant increase of the redox potential of lithiated organic electrode materials. This is achieved by tuning the electronic effects in the redox-active organic skeleton thanks to the permanent presence of a spectator cation in the host structure exhibiting a high ionic potential (or electronegativity). Thus, substituting magnesium (2,5-dilithium-oxy)-terephthalate for lithium (2,5-dilithium-oxy)-terephthalate enables a voltage gain of nearly +800 mV. This compound being also able to act as negative electrode via the carboxylate functional groups, an all-organic symmetric lithium-ion cell exhibiting an output voltage of 2.5 V is demonstrated. |
format | Online Article Text |
id | pubmed-6199296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61992962018-10-25 Raising the redox potential in carboxyphenolate-based positive organic materials via cation substitution Jouhara, Alia Dupré, Nicolas Gaillot, Anne-Claire Guyomard, Dominique Dolhem, Franck Poizot, Philippe Nat Commun Article Meeting the ever-growing demand for electrical storage devices requires both superior and “greener” battery technologies. Nearly 40 years after the discovery of conductive polymers, long cycling stability in lithium organic batteries has now been achieved. However, the synthesis of high-voltage lithiated organic cathode materials is rather challenging, so very few examples of all-organic lithium-ion cells currently exist. Herein, we present an inventive chemical approach leading to a significant increase of the redox potential of lithiated organic electrode materials. This is achieved by tuning the electronic effects in the redox-active organic skeleton thanks to the permanent presence of a spectator cation in the host structure exhibiting a high ionic potential (or electronegativity). Thus, substituting magnesium (2,5-dilithium-oxy)-terephthalate for lithium (2,5-dilithium-oxy)-terephthalate enables a voltage gain of nearly +800 mV. This compound being also able to act as negative electrode via the carboxylate functional groups, an all-organic symmetric lithium-ion cell exhibiting an output voltage of 2.5 V is demonstrated. Nature Publishing Group UK 2018-10-23 /pmc/articles/PMC6199296/ /pubmed/30353001 http://dx.doi.org/10.1038/s41467-018-06708-x Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jouhara, Alia Dupré, Nicolas Gaillot, Anne-Claire Guyomard, Dominique Dolhem, Franck Poizot, Philippe Raising the redox potential in carboxyphenolate-based positive organic materials via cation substitution |
title | Raising the redox potential in carboxyphenolate-based positive organic materials via cation substitution |
title_full | Raising the redox potential in carboxyphenolate-based positive organic materials via cation substitution |
title_fullStr | Raising the redox potential in carboxyphenolate-based positive organic materials via cation substitution |
title_full_unstemmed | Raising the redox potential in carboxyphenolate-based positive organic materials via cation substitution |
title_short | Raising the redox potential in carboxyphenolate-based positive organic materials via cation substitution |
title_sort | raising the redox potential in carboxyphenolate-based positive organic materials via cation substitution |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199296/ https://www.ncbi.nlm.nih.gov/pubmed/30353001 http://dx.doi.org/10.1038/s41467-018-06708-x |
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