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High-performance lithium-ion battery anodes based on Mn3O4/nitrogen-doped porous carbon hybrid structures
Manganese oxide is a promising anode material in next-generation rechargeable batteries due to its high theoretical specific capacity and low reduction potential. Here we report a facile and scalable approach to fabricate the novel Mn3O4 and nitrogen-doped porous carbon hybrid nanocomposite (Mn3O4/C...
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Published in: | Journal of alloys and compounds 2019-02, Vol.775, p.51-58 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Manganese oxide is a promising anode material in next-generation rechargeable batteries due to its high theoretical specific capacity and low reduction potential. Here we report a facile and scalable approach to fabricate the novel Mn3O4 and nitrogen-doped porous carbon hybrid nanocomposite (Mn3O4/CN) as lithium-ion battery anodes. The obtained nanocomposite has numerous nanosized Mn3O4 nanoparticles (∼30 nm), which are uniformly dispersed in N-doped porous carbon matrix (the N content is ∼12.2%). The N-doped porous carbon matrix can not only improve the electronic conductivity and increase the Li+ storage active sites, but also accommodate the structural stress generated by volume change of Mn3O4 nanoparticles during cycling. Remarkably, the Mn3O4/CN anode exhibits long-term cycling stability for a reversible discharge capacity of 945 mA h g−1 (the specific capacity is calculated using the mass of the whole hybrid) at a current density of 1 A g−1 after 400 cycles, indicating a capacity retention of 94.7%. The Mn3O4/CN anode with excellent performance shows its immense potential for lithium-ion batteries.
•Synthesis of Mn3O4 and N-doped porous carbon network hybrid nanocomposite.•The Mn3O4/CN anode delivers 945 mA h g−1 at 1 A g−1 after 400 cycles.•The Mn3O4/CN anode exhibits excellent rate performance. |
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ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2018.10.106 |