Phenothiazine Dimer as Efficient and Recyclable p‐Type Organic Positive Electrode Material for Anion‐Ion and Dual‐Ion Batteries

This article presents the electrochemical properties of a series of phenothiazine and phenoxazine dimers, by involving an aromatic central core, efficiently synthesized in a single step through a Buckwald–Hartwig coupling reaction. A synergistic approach combining experimental and quantum chemical studies was used in view of providing a thorough characterization of their capabilities as electrodes in the context of electrochemical energy storage applications. A detailed study of the electrochemical activity was then conducted with the aim of optimizing performance, i.e., achieving a specific capacity of around 100 mAh.g −1 , close to the theoretical values at a potential of 3.6 V relative to Li metal. The dimerization strategy also emerged as an interesting methodology, since it gives rise to molecular materials having specific solubility properties. This finding opens up the possibility of recovering the active material from the electrode at the end of its life, thus paving the way for improved organic electrodes and batteries, especially with respect to their recyclable character.

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Publication Details

Journal
Batteries & Supercaps
Published
2025-09-08
DOI
https://doi.org/10.1002/batt.202500403
Citations
1
Primary Topic
Phenothiazines and Benzothiazines Synthesis and Activities
Type
article
Field-Weighted Citation Impact
0.81

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article

Phenothiazine Dimer as Efficient and Recyclable p‐Type Organic Positive Electrode Material for Anion‐Ion and Dual‐Ion Batteries

Christine Frayret, Sylvestre Toumieux, Yann Danten, Carlo Gatti et al.
1 citations
Batteries & Supercaps
Phenothiazines and Benzothiazines Synthesis and Activities
0.81
article

Phenothiazine Dimer as Efficient and Recyclable p‐Type Organic Positive Electrode Material for Anion‐Ion and Dual‐Ion Batteries

Christine Frayret, Sylvestre Toumieux, Yann Danten, Carlo Gatti, Matthieu Bécuwe, Murugesan Rajesh, Seybou Hassane Diallo
article en
1 citations

Abstract

This article presents the electrochemical properties of a series of phenothiazine and phenoxazine dimers, by involving an aromatic central core, efficiently synthesized in a single step through a Buckwald–Hartwig coupling reaction. A synergistic approach combining experimental and quantum chemical studies was used in view of providing a thorough characterization of their capabilities as electrodes in the context of electrochemical energy storage applications. A detailed study of the electrochemical activity was then conducted with the aim of optimizing performance, i.e., achieving a specific capacity of around 100 mAh.g −1 , close to the theoretical values at a potential of 3.6 V relative to Li metal. The dimerization strategy also emerged as an interesting methodology, since it gives rise to molecular materials having specific solubility properties. This finding opens up the possibility of recovering the active material from the electrode at the end of its life, thus paving the way for improved organic electrodes and batteries, especially with respect to their recyclable character.

Batteries & SupercapsVol. 9(1)
Centre National de la Recherche Scientifique (FR), Institut des Sciences Moléculaires (FR), Réseau sur le Stockage Electrochimique de l'énergie (FR), Laboratoire de Glycochimie, des Antimicrobiens et des Agroressources (FR), Laboratoire de Réactivité et Chimie des Solides (FR), Institute of Molecular Science and Technologies (IT), Tecnologie Avanzate (Italy) (IT), Université de Picardie Jules Verne (FR)
Agence Nationale de la Recherche, Université de Bordeaux, Grand Équipement National De Calcul Intensif
Openalex Percentile: Top 24%
Phenothiazines and Benzothiazines Synthesis and Activities
0.81
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