Nickel Complex Based Electrodes for Li‐ion Batteries

Abstract This work focuses on the development of nickel‐based quinone complexes as electrode materials for next‐generation rechargeable batteries. These complexes were synthesized with different substituents and their potential as anode materials in lithium‐based systems was investigated. Scanning electron microscopy (SEM) and energy‐dispersive X‐ray spectroscopy (EDX) confirmed the uniform distribution and composition of the electrode materials deposited by spin coating. Comprehensive electrochemical testing, including galvanostatic charge‐discharge cycling and impedance spectroscopy, showed that the dinickel complex 2 a present low capacity (10 mA h g −1 ) while the 2 b presents a maximum specific capacity up to 28 mA h g −1 at 0.4 C and very good stability over more than 200 cycles. Analogue 2 c exhibited a maximum specific capacity up to 25 mA h g −1 at 0.2 C, maintaining high cycling stability across different C‐rates but significantly lower capacity at higher C‐rates, indicating mass transport limitations.

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Publication Details

Journal
European Journal of Inorganic Chemistry
Published
2024-12-06
DOI
https://doi.org/10.1002/ejic.202400649
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
0.00

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article

Nickel Complex Based Electrodes for Li‐ion Batteries

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European Journal of Inorganic Chemistry
Advancements in Battery Materials
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Nickel Complex Based Electrodes for Li‐ion Batteries

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article en

Abstract

Abstract This work focuses on the development of nickel‐based quinone complexes as electrode materials for next‐generation rechargeable batteries. These complexes were synthesized with different substituents and their potential as anode materials in lithium‐based systems was investigated. Scanning electron microscopy (SEM) and energy‐dispersive X‐ray spectroscopy (EDX) confirmed the uniform distribution and composition of the electrode materials deposited by spin coating. Comprehensive electrochemical testing, including galvanostatic charge‐discharge cycling and impedance spectroscopy, showed that the dinickel complex 2 a present low capacity (10 mA h g −1 ) while the 2 b presents a maximum specific capacity up to 28 mA h g −1 at 0.4 C and very good stability over more than 200 cycles. Analogue 2 c exhibited a maximum specific capacity up to 25 mA h g −1 at 0.2 C, maintaining high cycling stability across different C‐rates but significantly lower capacity at higher C‐rates, indicating mass transport limitations.

European Journal of Inorganic ChemistryVol. 28(3)
Centre National de la Recherche Scientifique (FR), Aix-Marseille Université (FR), Turin Polytechnic University (UZ), Centre Interdisciplinaire de Nanoscience de Marseille (FR)
Agence Nationale de la Recherche, Centre National de la Recherche Scientifique
Affordable and clean energy
Openalex Percentile: Top 80%
Advancements in Battery Materials
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