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Superior conductive 1D and 2D network structured carbon-coated Ni-rich Li 1.05 Ni 0.88 Co 0.08 Mn 0.04 O 2 as high-ion-diffusion cathodes for lithium-ion batteries

Numerous studies have addressed the low electrical conductivity of Li Ni Co Mn O (Ni-rich NCM). Among these approaches, surface treatment using multiwalled carbon nanotubes (MWCNTs) has emerged as a promising strategy for enhancing the depolarization of Ni-rich NCM and improving its electrochemical...

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Bibliographic Details
Published in:Physical chemistry chemical physics : PCCP 2024-12, Vol.27 (1), p.254-260
Main Authors: Na, Sungmin, Park, Junwoo, An, Hyunjin, Lee, Seonhwa, Yu, Byongyong, Park, Kwangjin
Format: Article
Language:English
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Summary:Numerous studies have addressed the low electrical conductivity of Li Ni Co Mn O (Ni-rich NCM). Among these approaches, surface treatment using multiwalled carbon nanotubes (MWCNTs) has emerged as a promising strategy for enhancing the depolarization of Ni-rich NCM and improving its electrochemical performance. However, MWCNT coatings applied by various methods often result in agglomeration and increase the ion-transfer resistance of the coating layer, leading to degraded electrochemical performance. In this study, 1D and 2D network structures are assembled on Ni-rich NCM surfaces using a MWCNT solution dispersed in ethanol solvent by an incipient method. The resulting highly conductive network structure facilitates electron movement without interfering with Li-ion transport, enhancing the depolarization of Ni-rich NCM and enabling high electrochemical performance. The 1D and 2D network structure coated Ni-rich NCM exhibits an excellent rate capability of 87.64% at 3C/0.2C and a cycle retention of 94.53% after 50 cycles at 1C/1C. Moreover, the incipient method used herein effectively maximizes the electrochemical performance with less coating weight than other methods. These findings highlight the potential of the 1D and 2D network structure coated Ni-rich NCM for advanced energy storage applications.
ISSN:1463-9076
1463-9084
DOI:10.1039/d4cp03144j