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Controllable preparation of one-dimensional Li(1.2)Mn(0.54)Ni(0.13)Co(0.13)O(2) cathode materials for high-performance lithium-ion batteries
Lithium-rich layered oxides are attractive candidates of high-energy-density cathode materials for high-performance lithium ion batteries because of their high specific capacity and low cost. Nevertheless, their unsatisfactory rate capability and poor cycling stability have strongly hindered commerc...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8694466/ https://www.ncbi.nlm.nih.gov/pubmed/35424457 http://dx.doi.org/10.1039/d0ra09880a |
Sumario: | Lithium-rich layered oxides are attractive candidates of high-energy-density cathode materials for high-performance lithium ion batteries because of their high specific capacity and low cost. Nevertheless, their unsatisfactory rate capability and poor cycling stability have strongly hindered commercial applications in lithium ion batteries, mainly due to the ineffectiveness of the complicated synthesis techniques to control their morphologies and sizes. In this work, the Li(1.2)Mn(0.54)Ni(0.13)Co(0.13)O(2) cathode materials with a one-dimensional rod-like morphology were synthesized via a facile co-precipitation route followed by a post-calcination treatment. By reasonably adding NH(3)·H(2)O in the co-precipitation reaction, the sizes of the metal oxalate precursors could be rationally varied. The electrochemical measurements displayed that the Li(1.2)Mn(0.54)Ni(0.13)Co(0.13)O(2) short rods delivered a high capacity of 286 mA h g(−1) at 0.1C and excellent capacity retention of 85% after 100 cycles, which could be contributed to the improvement of the electrolyte contact, Li(+) diffusion, and structural stability of the one-dimension porous structure. |
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