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Nickel Complex Based Electrodes for Li‐ion Batteries

Luca PasquiniAix Marseille Univ. CNRS MADIREL (UMR 7246) and International Laboratory: Ionomer Materials for Energy Campus St Jérôme 13013 Marseille FranceSurafel Mustefa BeyanAix Marseille Univ. CNRS CINaM (UMR 7325) Campus Luminy 13288 cedex 09 Marseille FranceAnvar KhamidovTurin Polytechnic University in Tashkent Department of Natural and Mathematical Science 100095 Tashkent City UzbekistanValentin JubaultAix Marseille Univ. CNRS CINaM (UMR 7325) Campus Luminy 13288 cedex 09 Marseille FranceTatiana MunteanuAix Marseille Univ. CNRS CINaM (UMR 7325) Campus Luminy 13288 cedex 09 Marseille FranceGabriel CanardAix Marseille Univ. CNRS CINaM (UMR 7325) Campus Luminy 13288 cedex 09 Marseille FrancePhilippe KnauthAix Marseille Univ. CNRS MADIREL (UMR 7246) and International Laboratory: Ionomer Materials for Energy Campus St Jérôme 13013 Marseille FranceOlivier SiriCentre Interdisciplinaire de Nanoscience de Marseille
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Аннотация

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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