Highly uniform nitrogen-doped carbon decorated MoO2 nanopopcorns as anode for high-performance lithium/sodium-ion storage

[Display omitted] •Highly uniform nitrogen-doped carbon decorated MoO2 nanopopcorns as anode for lithium/sodium-ion storage.•The facile synthesis involves self-templated solvothermal, double-annealing treatment and in-situ pyrolysis of polypyrrole.•The N-doped carbon shell confines MoO2 nanopopcorns...

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Veröffentlicht in:Journal of colloid and interface science 2020-03, Vol.563, p.318-327
Hauptverfasser: Zhang, Peilin, Guo, Shouzhi, Liu, Jinzhe, Zhou, Chencheng, Li, Shuo, Yang, Yun, Wu, Jing, Yu, Di, Chen, Luyang
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Sprache:eng
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Zusammenfassung:[Display omitted] •Highly uniform nitrogen-doped carbon decorated MoO2 nanopopcorns as anode for lithium/sodium-ion storage.•The facile synthesis involves self-templated solvothermal, double-annealing treatment and in-situ pyrolysis of polypyrrole.•The N-doped carbon shell confines MoO2 nanopopcorns with high structural integrity and electrical conductivity. Molybdenum dioxides (MoO2) featuring low cost and high theoretical capacity endow them competitive anode materials for lithium-ion batteries (LIBs)/sodium-ion batteries (SIBs). However, the low electrical conductivity and severe volume expansion occurring during the ion insertion/extraction process hamper their practical application. Herein, a novel dual-annealing design has been developed for the synthesis of highly uniform MoO2 nanopopcorns decorated with nitrogen-doped carbon shell (MoO2/NC). Owing to the unique structural characteristics and vital amorphous NC component, the MoO2/NC nanopopcorn hybrid composite exhibits stabilized charge storage capacity of 1073 mAh g−1 after 200 cycles for LIBs, while 301 mAh g−1 after 500 cycles for SIBs at 0.5 A g−1. Furthermore, when the current density increases to 5 A g−1, the specific capacity could still maintain 630 mAh g−1 and 174 mAh g−1 for LIBs and SIBs, respectively, which disclose the outstanding rate capability of MoO2/NC nanopopcorn anode.
ISSN:0021-9797
1095-7103
DOI:10.1016/j.jcis.2019.12.062