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Molybdenum Oxynitride Atomic Nanoclusters Bonded in Nanosheets of N-Doped Carbon Hierarchical Microspheres for Efficient Sodium Storage
Transition metal nitrides have attracted considerable attention as great potential anode materials due to their excellent metallic conductivity and high theoretical specific capacity. However, their cycling performance is impeded by their instability caused by the reaction mechanism. Herein, we repo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Nature Singapore
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9375813/ https://www.ncbi.nlm.nih.gov/pubmed/35962882 http://dx.doi.org/10.1007/s40820-022-00893-7 |
Sumario: | Transition metal nitrides have attracted considerable attention as great potential anode materials due to their excellent metallic conductivity and high theoretical specific capacity. However, their cycling performance is impeded by their instability caused by the reaction mechanism. Herein, we report the engineering and synthesis of a novel hybrid architecture composed of MoO(2.0)N(0.5) atomic nanoclusters bonded in nanosheets of N-doped carbon hierarchical hollow microspheres (MoO(2.0)N(0.5)/NC) as an anode material for sodium-ion batteries. The facile self-templating strategy for the synthesis of MoO(2.0)N(0.5)/NC involves chemical polymerization and subsequent one-step calcination treatments. The design is beneficial to improve the electrochemical kinetics, buffer the volume variation of electrodes during cycling, and provide more interfacial active sites for sodium uptake. Due to these unique structural and compositional merits, these MoO(2.0)N(0.5)/NC exhibits excellent sodium storage performance in terms of superior rate capability and stable long cycle life. The work shows a feasible and effective way to design novel host candidates and solve the long-term cycling stability issues for sodium-ion batteries. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40820-022-00893-7. |
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