Cargando…
Benzidine Derivatives as Electroactive Materials for Aqueous Organic Redox Flow Batteries
[Image: see text] This paper presents a theoretical and experimental evaluation of benzidine derivatives as electroactive molecules for organic redox flow batteries. These redox indicators are novel electroactive materials that can perform multielectron transfers in aqueous media. We performed the s...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10500672/ https://www.ncbi.nlm.nih.gov/pubmed/37720753 http://dx.doi.org/10.1021/acsomega.3c02297 |
_version_ | 1785105958558498816 |
---|---|
author | Flores-Leonar, Martha M. Acosta-Tejada, Gloria Laguna, Humberto G. Amador-Bedolla, Carlos Sánchez-Castellanos, Mariano Ugalde-Saldívar, Víctor M. |
author_facet | Flores-Leonar, Martha M. Acosta-Tejada, Gloria Laguna, Humberto G. Amador-Bedolla, Carlos Sánchez-Castellanos, Mariano Ugalde-Saldívar, Víctor M. |
author_sort | Flores-Leonar, Martha M. |
collection | PubMed |
description | [Image: see text] This paper presents a theoretical and experimental evaluation of benzidine derivatives as electroactive molecules for organic redox flow batteries. These redox indicators are novel electroactive materials that can perform multielectron transfers in aqueous media. We performed the synthesis, electrochemical characterization, and theoretical study of the dimer of sodium 4-diphenylamine sulfonate, a benzidine derivative with high water solubility properties. The Pourbaix diagram of the dimer shows a bielectronic process at highly acidic pH values (≤ 0.9) and two single-electron transfers in a pH range from 0 to 9. The dimer was prepared in situ and tested on a neutral electrochemical flow cell as a stability diagnostic. To improve cell performance, we calculate and calibrate, with experimental data, the Pourbaix diagrams of benzidine derivatives using different substitution patterns and functional groups. A screening process allowed the selection of those derivatives with a bielectronic process in the entire pH window or at acidic/neutral pH values. Given the redox potential difference, they can be potential catholytes or anolytes in a flow cell. The couples formed with the final candidates can generate a theoretical cell voltage of 0.60 V at pH 0 and up to 0.68 V at pH 7. These candidate molecules could be viable as electroactive materials for a full-organic redox flow battery. |
format | Online Article Text |
id | pubmed-10500672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-105006722023-09-15 Benzidine Derivatives as Electroactive Materials for Aqueous Organic Redox Flow Batteries Flores-Leonar, Martha M. Acosta-Tejada, Gloria Laguna, Humberto G. Amador-Bedolla, Carlos Sánchez-Castellanos, Mariano Ugalde-Saldívar, Víctor M. ACS Omega [Image: see text] This paper presents a theoretical and experimental evaluation of benzidine derivatives as electroactive molecules for organic redox flow batteries. These redox indicators are novel electroactive materials that can perform multielectron transfers in aqueous media. We performed the synthesis, electrochemical characterization, and theoretical study of the dimer of sodium 4-diphenylamine sulfonate, a benzidine derivative with high water solubility properties. The Pourbaix diagram of the dimer shows a bielectronic process at highly acidic pH values (≤ 0.9) and two single-electron transfers in a pH range from 0 to 9. The dimer was prepared in situ and tested on a neutral electrochemical flow cell as a stability diagnostic. To improve cell performance, we calculate and calibrate, with experimental data, the Pourbaix diagrams of benzidine derivatives using different substitution patterns and functional groups. A screening process allowed the selection of those derivatives with a bielectronic process in the entire pH window or at acidic/neutral pH values. Given the redox potential difference, they can be potential catholytes or anolytes in a flow cell. The couples formed with the final candidates can generate a theoretical cell voltage of 0.60 V at pH 0 and up to 0.68 V at pH 7. These candidate molecules could be viable as electroactive materials for a full-organic redox flow battery. American Chemical Society 2023-08-31 /pmc/articles/PMC10500672/ /pubmed/37720753 http://dx.doi.org/10.1021/acsomega.3c02297 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Flores-Leonar, Martha M. Acosta-Tejada, Gloria Laguna, Humberto G. Amador-Bedolla, Carlos Sánchez-Castellanos, Mariano Ugalde-Saldívar, Víctor M. Benzidine Derivatives as Electroactive Materials for Aqueous Organic Redox Flow Batteries |
title | Benzidine Derivatives
as Electroactive Materials for
Aqueous Organic Redox Flow Batteries |
title_full | Benzidine Derivatives
as Electroactive Materials for
Aqueous Organic Redox Flow Batteries |
title_fullStr | Benzidine Derivatives
as Electroactive Materials for
Aqueous Organic Redox Flow Batteries |
title_full_unstemmed | Benzidine Derivatives
as Electroactive Materials for
Aqueous Organic Redox Flow Batteries |
title_short | Benzidine Derivatives
as Electroactive Materials for
Aqueous Organic Redox Flow Batteries |
title_sort | benzidine derivatives
as electroactive materials for
aqueous organic redox flow batteries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10500672/ https://www.ncbi.nlm.nih.gov/pubmed/37720753 http://dx.doi.org/10.1021/acsomega.3c02297 |
work_keys_str_mv | AT floresleonarmartham benzidinederivativesaselectroactivematerialsforaqueousorganicredoxflowbatteries AT acostatejadagloria benzidinederivativesaselectroactivematerialsforaqueousorganicredoxflowbatteries AT lagunahumbertog benzidinederivativesaselectroactivematerialsforaqueousorganicredoxflowbatteries AT amadorbedollacarlos benzidinederivativesaselectroactivematerialsforaqueousorganicredoxflowbatteries AT sanchezcastellanosmariano benzidinederivativesaselectroactivematerialsforaqueousorganicredoxflowbatteries AT ugaldesaldivarvictorm benzidinederivativesaselectroactivematerialsforaqueousorganicredoxflowbatteries |