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Ultrafast synthesis of spinel AMn2O4 (A= Co, Mn, Zn) nanopolyhedras and their composites applied to lithium ion battery anode

Spinel oxide anode materials are hardly used for commercial lithium-ion batteries because of their evident volume expansion in the discharging process and poor electronic conduction. Preparing a composite material of nanostructured spinel bimetallic oxides and carbon will solve the above problems an...

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Bibliographic Details
Published in:Journal of alloys and compounds 2024-06, Vol.987, p.174212, Article 174212
Main Authors: Zhang, Dan, Zhang, Chunyan, Xu, Huishi, Huo, Zhe, Shi, Xinyu, Luo, Baomin, Liu, Guangyin, Liu, Xiaodi, Li, Liping, Yu, Chuang
Format: Article
Language:English
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Summary:Spinel oxide anode materials are hardly used for commercial lithium-ion batteries because of their evident volume expansion in the discharging process and poor electronic conduction. Preparing a composite material of nanostructured spinel bimetallic oxides and carbon will solve the above problems and achieve outstanding electrochemical performance. In this study, an ultrafast approach (only 10 min) to synthesize spinel AMn2O4 (A= Co, Mn, Zn) nanopolyhedras and their composites with GO was successfully developed. Integrating spinel CoMn2O4 nanopolyhedras with GO can profoundly inhibit the problem of volume expansion but also eminently upgrading conductivity. The CoMn2O4/GO composite anode displays competent cyclic life and rate capability for lithium ion battery, delivering a large capacity of 738 mAh g−1 after 340 cycles at 2 A g−1. The ultrafast approach and alluring electrochemical performance of this work will inevitably give impetus to the fast development and application of spinel oxides. [Display omitted] •Spinel CoMn2O4 and CoMn2O4/GO were synthesized by an ultrafast method.•The ultrafast synthetic method can be expanded to other spinel oxides.•Nanopolyhedras grown on GO leads to the alluring electrochemical performance.•High capacity of 738 mA h g−1 after 340 cycles is achieved at 2 A g−1.
ISSN:0925-8388
1873-4669
DOI:10.1016/j.jallcom.2024.174212